Nutritionally Mediated Programming of the Developing Immune System

Immunobiology: the immune system in health and disease

(1995) · Choice Reviews Online · doi:10.5860/choice.32-3876 · Cited by 4,110 · see citing works

WEIGHT IN INFANCY AND DEATH FROM ISCHAEMIC HEART DISEASE

Barker, D. J. P., Osmond, C., Winter, P. D., Margetts, B., & Simmonds, S. J. (1989) · The Lancet · doi:10.1016/s0140-6736(89)90710-1 · Cited by 3,574 · see citing works

Towards a network theory of the immune system.

Nk, J. (1974) · PubMed · Cited by 3,388 · see citing works

The origins of the developmental origins theory

Barker, D. J. P. (2007) · Journal of Internal Medicine · doi:10.1111/j.1365-2796.2007.01809.x · Cited by 2,955 · see citing works

Bidirectional cytokine interactions in the maternal-fetal relationship: is successful pregnancy a TH2 phenomenon?

Wegmann, T. G., Lin, H., Guilbert, L., & Mosmann, T. R. (1993) · Immunology Today · doi:10.1016/0167-5699(93)90235-d · Cited by 2,852 · see citing works

Growth in utero, blood pressure in childhood and adult life, and mortality from cardiovascular disease.

Barker, D. J., Osmond, C., Golding, J., Kuh, D., & Wadsworth, M. E. (1989) · BMJ · doi:10.1136/bmj.298.6673.564 · Cited by 2,415 · see citing works

The contribution of low birth weight to infant mortality and childhood morbidity

McCormick, M. C. (1985) · New England Journal of Medicine · doi:10.1056/nejm198501103120204 · Cited by 2,119 · see citing works

Promotion of Breastfeeding Intervention Trial (PROBIT)

Kramer, M. S., CHALMERS, B. E., HODNETT, E. D., Sevkovskaya, Z., Dzikovich, I., Shapiro, S. H., Collet, J., Vanilovich, I., Mezen, I., Ducruet, T., et al. (2001) · JAMA · doi:10.1001/jama.285.4.413 · Cited by 1,536 · see citing works

Glucocorticoid activation of a calcium-dependent endonuclease in thymocyte nuclei leads to cell death.

Cohen, J., & Duke, R. C. (1984) · The Journal of Immunology · doi:10.4049/jimmunol.132.1.38 · Cited by 1,406 · see citing works

Principles of Anatomy and Physiology

Baker, G. F., Tortora, G. J., & Nostakos, N. P. A. (1976) · AJN American Journal of Nursing · doi:10.2307/3423898 · Cited by 1,322 · see citing works

Effect of Corticosteroids for Fetal Maturation on Perinatal Outcomes: NIH Consensus Development Panel on the Effect of Corticosteroids for Fetal Maturation on Perinatal Outcomes

Gilstrap, L. C. (1995) · JAMA · doi:10.1001/jama.1995.03520290065031 · Cited by 1,269 · see citing works

Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum

Bianchi, D. W., Zickwolf, G. K., Weil, G. J., Sylvester, S., & DeMaria, M. A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.2.705 · Cited by 1,264 · see citing works

CARBOPLATIN OR CISPLATIN?

Calvert, H., Horwich, A., Newlands, E. S., Beǵent, R. H. J., Rustin, G. J. S., Kaye, S. B., Harris, A. L., Williams, C. J., & Slevin, M. L. (1988) · The Lancet · doi:10.1016/s0140-6736(88)92709-2 · Cited by 1,183 · see citing works

γδ Cells: A Right Time and a Right Place for a Conserved Third Way of Protection

Hayday, A. (2000) · Annual Review of Immunology · doi:10.1146/annurev.immunol.18.1.975 · Cited by 1,134 · see citing works

Effect of breastfeeding on infant and child mortality due to infectious diseases in less developed countries: a pooled analysis

Victora, C. G., Fontaine, O., Morris, S., Schellenburg, J., Gray, R., Black, R., Borros, A., Ashraf, R., Morris, J., Fucks, S., et al. (2000) · The Lancet · doi:10.1016/s0140-6736(00)82011-5 · Cited by 1,058 · see citing works

Delayed Breastfeeding Initiation Increases Risk of Neonatal Mortality

Edmond, K. M., Zandoh, C., QUIGLEY, M. A., Amenga‐Etego, S., Owusu‐Agyei, S., & Kirkwood, B. R. (2006) · PEDIATRICS · doi:10.1542/peds.2005-1496 · Cited by 1,057 · see citing works

Function of the retinoic acid receptors (RARs) during development: (II) Multiple abnormalities at various stages of organogenesis in RAR double mutants

Mendelsohn, C. L., Lohnes, D., Décimo, D., Lufkin, T., LeMeur, M., Chambon, P., & Mark, M. P. (1994) · Development · doi:10.1242/dev.120.10.2749 · Cited by 990 · see citing works

γδ T cell effector functions: a blend of innate programming and acquired plasticity

Bonneville, M., O'Brien, R. L., & Born, W. K. (2010) · Nature Reviews Immunology · doi:10.1038/nri2781 · Cited by 952 · see citing works

Nutritional and physiologic significance of human milk proteins

Lönnerdal, B. L. (2003) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/77.6.1537s · Cited by 879 · see citing works

Maternal Alloantigens Promote the Development of Tolerogenic Fetal Regulatory T Cells in Utero

Mold, J. E., Michaëlsson, J., Burt, T. D., Muench, M. O., Beckerman, K., Busch, M. P., Lee, T., Nixon, D. F., & McCune, J. M. (2008) · Science · doi:10.1126/science.1164511 · Cited by 840 · see citing works

Some immunological and endocrinological problems raised by the evolution of viviparity in verte- brates

Medawar, P. B., & Medawar, P. B. (1953) · Symposia of the Society for Experimental Biology · Cited by 833 · see citing works

MALARIAL DIABETES

Rau, L. (1948) · The Lancet · doi:10.1016/s0140-6736(48)91789-9 · Cited by 826 · see citing works

Gamma/Delta Cells

Haas, W., Pereira, P., & Tonegawa, S. (1993) · Annual Review of Immunology · doi:10.1146/annurev.iy.11.040193.003225 · Cited by 808 · see citing works

Placental transport of immunoglobulin G

Simister, N. (2003) · Vaccine · doi:10.1016/s0264-410x(03)00334-7 · Cited by 783 · see citing works

V ITAMIN A, I NFECTION , AND I MMUNE F UNCTION *

Stephensen, C. B. (2001) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.21.1.167 · Cited by 776 · see citing works

Natural autoantibodies: from ‘horror autotoxicus’ to ‘gnothi seauton’

Avrameas, S. (1991) · Immunology Today · doi:10.1016/s0167-5699(05)80045-3 · Cited by 766 · see citing works

Organogenesis of lymphoid tissues

Mebius, R. E. (2003) · Nature reviews. Immunology · doi:10.1038/nri1054 · Cited by 747 · see citing works

Breastfeeding as prophylaxis against atopic disease: prospective follow-up study until 17 years old

Saarinen, U. M., & Kajosaari, M. (1995) · The Lancet · doi:10.1016/s0140-6736(95)91742-x · Cited by 710 · see citing works

B-1a and B-1b Cells Exhibit Distinct Developmental Requirements and Have Unique Functional Roles in Innate and Adaptive Immunity to S. pneumoniae

Haas, K. M., Poe, J. C., Steeber, D. A., & Tedder, T. F. (2005) · Immunity · doi:10.1016/j.immuni.2005.04.011 · Cited by 628 · see citing works

New insights into the development of lymphoid tissues

van de Pavert, S. A., & Mebius, R. E. (2010) · Nature reviews. Immunology · doi:10.1038/nri2832 · Cited by 597 · see citing works

The journey of developing hematopoietic stem cells

Mikkola, H. K. A., & Orkin, S. H. (2006) · Development · doi:10.1242/dev.02568 · Cited by 577 · see citing works

Natural autoantibodies

Coutinho, A., Kazatchkine, M. D., & Avraméas, S. (1995) · Current Opinion in Immunology · doi:10.1016/0952-7915(95)80053-0 · Cited by 574 · see citing works

Leptin protects mice from starvation-induced lymphoid atrophy and increases thymic cellularity in ob/ob mice

Howard, J. K., Lord, G. M., Matarese, G., Vendetti, S., Ghatei, M. A., Ritter, M. A., Lechler, R. I., & Bloom, S. R. (1999) · Journal of Clinical Investigation · doi:10.1172/jci6762 · Cited by 566 · see citing works

microRNA as a new immune-regulatory agent in breast milk

Kosaka, N., Izumi, H., Sekine, K., & Ochiya, T. (2010) · Silence · doi:10.1186/1758-907x-1-7 · Cited by 563 · see citing works

Evolution of Maternofetal Transport of Immunoglobulins During Human Pregnancy

Malek, A., Sager, R., Kuhn, P., Nicolaides, K. H., & Schneider, H. (1996) · American Journal of Reproductive Immunology · doi:10.1111/j.1600-0897.1996.tb00172.x · Cited by 559 · see citing works

Inherent specificities in natural antibodies: a key to immune defense against pathogen invasion

Baumgarth, N., Tung, J. W., & Herzenberg, L. A. (2005) · Springer Seminars in Immunopathology · doi:10.1007/s00281-004-0182-2 · Cited by 545 · see citing works

Role of the placenta in fetal programming: underlying mechanisms and potential interventional approaches

Jansson, T., & Powell, T. L. (2007) · Clinical Science · doi:10.1042/cs20060339 · Cited by 542 · see citing works

Mechanisms of nutrient modulation of the immune response

Cunningham–Rundles, S., McNeeley, D. F., & Moon, A. (2005) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2005.04.036 · Cited by 535 · see citing works

Early programming of the hypothalamo–pituitary–adrenal axis

MATTHEWS, S. (2002) · Trends in Endocrinology and Metabolism · doi:10.1016/s1043-2760(02)00690-2 · Cited by 513 · see citing works

Association between breast feeding and asthma in 6 year old children: findings of a prospective birth cohort study

Oddy, W. H., Holt, P. G., Sly, P. D., Read, A. W., Landau, L. I., Stanley, F., Kendall, G. E., & Burton, P. R. (1999) · BMJ · doi:10.1136/bmj.319.7213.815 · Cited by 510 · see citing works

Actions of Placental and Fetal Adrenal Steroid Hormones in Primate Pregnancy*

Pepe, G. J., & Albrecht, E. D. (1995) · Endocrine Reviews · doi:10.1210/edrv-16-5-608 · Cited by 491 · see citing works

Immunofluorescent studies of the development of pre‐B cells, B lymphocytes and immunoglobulin isotype diversity in humans

Gathings, W. E., Lawton, A. R., & Cooper, M. D. (1977) · European Journal of Immunology · doi:10.1002/eji.1830071112 · Cited by 486 · see citing works

Reprogramming of the immune system during zinc deficiency

Fraker, P. J., & King, L. E. (2004) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.24.012003.132454 · Cited by 470 · see citing works

THE TRANSMISSION OF IMMUNITY FROM MOTHER TO YOUNG AND THE CATABOLISM OF IMMUNOGLOBULINS

Brambell, F. W. R. (1966) · The Lancet · doi:10.1016/s0140-6736(66)92190-8 · Cited by 463 · see citing works

Fetal and Adult Hematopoietic Stem Cells Give Rise to Distinct T Cell Lineages in Humans

Mold, J. E., Venkatasubrahmanyam, S., Burt, T. D., Michaëlsson, J., Rivera, J. M., Galkina, S. A., Weinberg, K., Stoddart, C. A., & McCune, J. M. (2010) · Science · doi:10.1126/science.1196509 · Cited by 444 · see citing works

Nutrients and their role in host resistance to infection

Field, C. J., Johnson, I. R., & Schley, P. D. (2002) · Journal of Leukocyte Biology · doi:10.1189/jlb.71.1.16 · Cited by 428 · see citing works

Identification of a B-1 B cell–specified progenitor

Montecino‐Rodriguez, E., Leathers, H., & Dorshkind, K. A. (2006) · Nature Immunology · doi:10.1038/ni1301 · Cited by 426 · see citing works

Embryonic retinoic acid synthesis is essential for heart morphogenesis in the mouse

Niederreither, K., Vermot, J., Messaddeq, N., Schuhbaur, B., Chambon, P., & Dollé, P. (2001) · Development · doi:10.1242/dev.128.7.1019 · Cited by 418 · see citing works

B1b Lymphocytes Confer T Cell-Independent Long-Lasting Immunity

Alugupalli, K. R., Leong, J. M., Woodland, R. T., Muramatsu, M., Honjo, T., & Gerstein, R. M. (2004) · Immunity · doi:10.1016/j.immuni.2004.06.019 · Cited by 411 · see citing works

Different roles of αβ and γδ T cells in immunity against an intracellular bacterial pathogen

Mombaerts, P., Arnoldi, J., Russ, F., Tonegawa, S., & Kaufmann, S. H. E. (1993) · Nature · doi:10.1038/365053a0 · Cited by 406 · see citing works

Transfer of antibody via mother's milk

de Perre, P. V. (2003) · Vaccine · doi:10.1016/s0264-410x(03)00336-0 · Cited by 405 · see citing works

Hormones and Growth Factors in Milk

GROSVENOR, C. E., Picciano, M. F., & Baumrucker, C. R. (1993) · Endocrine Reviews · doi:10.1210/edrv-14-6-710 · Cited by 404 · see citing works

Effect of breastfeeding on infant and child mortality due to infectious diseases in less developed countries: a pooled analysis. WHO Collaborative Study Team on the Role of Breastfeeding on the Prevention of Infant Mortality.

(2000) · PubMed · Cited by 404 · see citing works

Zinc deficiency and immune function.

Keen, C. L., & Gershwin, M. (1990) · Annual review of nutrition · doi:10.1146/annurev.nu.10.070190.002215 · Cited by 400 · see citing works

The many faces of the hygiene hypothesis

Schaub, B., Lauener, R. P., & von Mutius, E. (2006) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2006.03.003 · Cited by 380 · see citing works

The zebrafishnecklessmutation reveals a requirement forraldh2in mesodermal signals that pattern the hindbrain

Begemann, G., Schilling, T. F., Rauch, G.-J., Geisler, R., & Ingham, P. W. (2001) · Development · doi:10.1242/dev.128.16.3081 · Cited by 379 · see citing works

Early-life exposure to endotoxin alters hypothalamic-pituitary-adrenal function and predisposition to inflammation

Shanks, N., Windle, R. J., Perks, P. A., Harbuz, M. S., Jessop, D. S., Ingram, C. D., & Lightman, S. L. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.090571897 · Cited by 374 · see citing works

Isolation from human placenta of the IgG transporter, FcRn, and localization to the syncytiotrophoblast: implications for maternal-fetal antibody transport

Leach, J. L., Sedmak, D. D., Osborne, J. M., Rahill, B., Lairmore, M. D., & Anderson, C. L. (1996) · The Journal of Immunology · doi:10.4049/jimmunol.157.8.3317 · Cited by 348 · see citing works

Development of Secondary Lymphoid Organs

Randall, T. D., Carragher, D. M., & Rangel‐Moreno, J. (2008) · Annual Review of Immunology · doi:10.1146/annurev.immunol.26.021607.090257 · Cited by 339 · see citing works

Prenatal Stress Alters Bacterial Colonization of the Gut in Infant Monkeys

Bailey, M. T., Lubach, G. R., & Coe, C. L. (2004) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/00005176-200404000-00009 · Cited by 339 · see citing works

Programming placental nutrient transport capacity

Fowden, A. L., Ward, J. W., Wooding, F. P. B., Forhead, A. J., & Constancia, M. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2005.104141 · Cited by 334 · see citing works

SpsA, a novel pneumococcal surface protein with specific binding to secretory Immunoglobulin A and secretory component

Hammerschmidt, S., Talay, S. R., Brandtzæg, P., & Chhatwal, G. S. (1997) · Molecular Microbiology · doi:10.1046/j.1365-2958.1997.5391899.x · Cited by 332 · see citing works

Elevation of Cord over Maternal IgG Immunoglobulin: Evidence for an Active Placental IgG Transport

KOHLER, P. F., & FARR, R. S. (1966) · Nature · doi:10.1038/2101070a0 · Cited by 325 · see citing works

Mucosal immunity: integration between mother and the breast-fed infant

Brandtzaeg, P. (2003) · Vaccine · doi:10.1016/s0264-410x(03)00338-4 · Cited by 320 · see citing works

Mechanisms involved in the developmental programming of adulthood disease

Warner, M. J., & Ozanne, S. E. (2010) · Biochemical Journal · doi:10.1042/bj20091861 · Cited by 316 · see citing works

Impact of micronutrient supplementation during pregnancy on birth weight, duration of gestation, and perinatal mortality in rural western China: double blind cluster randomised controlled trial

Zeng, L., Cheng, Y., Dang, S., Yan, H., Dibley, M. J., Chang, S., & Kong, L. (2008) · BMJ · doi:10.1136/bmj.a2001 · Cited by 316 · see citing works

Differential development of progenitor activity for three B-cell lineages.

Kantor, A. B., Stall, A. M., Adams, S. D., Herzenberg, L. A., & Herzenberg, L. A. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.8.3320 · Cited by 314 · see citing works

Cohort study of peanut and tree nut sensitisation by age of 4 years

Tariq, S. M., Stevens, M., Matthews, S. P., Ridout, S., Twiselton, R., & Hide, D. W. (1996) · BMJ · doi:10.1136/bmj.313.7056.514 · Cited by 312 · see citing works

Season of birth predicts mortality in rural Gambia

Moore, S. E., Cole, T. J., Poskitt, E. M. E., Sonko, B. J., Whitehead, R. G., McGregor, I. A., & Prentice, A. M. (1997) · Nature · doi:10.1038/41245 · Cited by 311 · see citing works

Antenatal determinants of neonatal immune responses to allergens

Devereux, G. S., Barker, R. N., & Seaton, A. (2002) · Clinical & Experimental Allergy · doi:10.1046/j.0022-0477.2001.01267.x · Cited by 290 · see citing works

Structure and Function of Natural Antibodies

Casali, P., & Schettino, E. W. (1996) · Current topics in microbiology and immunology · doi:10.1007/978-3-642-85226-8_17 · Cited by 288 · see citing works

Markers to measure immunomodulation in human nutrition intervention studies

Albers, R., Antoine, J., Bourdet‐Sicard, R., Calder, P. C., Gleeson, M., Lesourd, B., Samartı́n, S., Sanderson, I. R., Loo, J. V., Dias, F. W. V., et al. (2005) · British Journal Of Nutrition · doi:10.1079/bjn20051469 · Cited by 284 · see citing works

Embryonic day 9 yolk sac and intra-embryonic hemogenic endothelium independently generate a B-1 and marginal zone progenitor lacking B-2 potential

Yoshimoto, M., Montecino‐Rodriguez, E., Ferkowicz, M. J., Porayette, P., Shelley, W. C., Conway, S. J., Dorshkind, K. A., & Yöder, M. C. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1015841108 · Cited by 283 · see citing works

Neonatal endotoxin exposure alters the development of the hypothalamic-pituitary-adrenal axis: early illness and later responsivity to stress

Shanks, N., Larocque, S., & Meaney, M. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-01-00376.1995 · Cited by 278 · see citing works

Early events in human T cell ontogeny. Phenotypic characterization and immunohistologic localization of T cell precursors in early human fetal tissues.

Haynes, B. F., Martin, M. E., Kay, H., & Kurtzberg, J. (1988) · The Journal of Experimental Medicine · doi:10.1084/jem.168.3.1061 · Cited by 270 · see citing works

Early nutrition and immunity - progress and perspectives.

Calder, P. C., Krauss‐Etschmann, S., de Jong, E. C., Dupont, C. M., Frick, J.-S., Frøkiær, H., Heinrich, J., Garn, H., Koletzko, S., Lack, G., et al. (2006) · PubMed · doi:10.1017/bjn20061917 · Cited by 269 · see citing works

Breast feeding and allergic diseases in infants--a prospective birth cohort study

Kull, I. (2002) · Archives of Disease in Childhood · doi:10.1136/adc.87.6.478 · Cited by 268 · see citing works

Low Maternal Vitamin E Intake during Pregnancy Is Associated with Asthma in 5-Year-Old Children

Devereux, G. S., Turner, S. W., Craig, L. C. A., McNeill, G., Martindale, S., Harbour, P. J., Helms, P. J. B., & Seaton, A. (2006) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200512-1946oc · Cited by 268 · see citing works

Modulation of the Immune System by Human Milk and Infant Formula Containing Nucleotides

Pickering, L. K., Granoff, D. M., Erickson, J. R., Masor, M. L., Cordle, C. T., Schaller, J. P., Winship, T. R., Paule, C. L., & Hilty, M. D. (1998) · PEDIATRICS · doi:10.1542/peds.101.2.242 · Cited by 266 · see citing works

Neonatal administration of idiotype or antiidiotype primes for protection against Escherichia coli K13 infection in mice.

Stein, K. E., & Söderström, T. (1984) · The Journal of Experimental Medicine · doi:10.1084/jem.160.4.1001 · Cited by 264 · see citing works

Secondary Lymphoid Organs: Responding to Genetic and Environmental Cues in Ontogeny and the Immune Response

Ruddle, N. H., & Akirav, E. M. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0804324 · Cited by 259 · see citing works

Toward a layered immune system

Herzenberg, L. A., & Herzenberg, L. A. (1989) · Cell · doi:10.1016/0092-8674(89)90748-4 · Cited by 258 · see citing works

Folic acid supplements in pregnancy and early childhood respiratory health

Håberg, S., London, S. J., Stigum, H., Nafstad, P. H. J., & Nystad, W. (2008) · Archives of Disease in Childhood · doi:10.1136/adc.2008.142448 · Cited by 256 · see citing works

Role of B-1a cells in autoimmunity

Duan, B., & Morel, L. (2006) · Autoimmunity Reviews · doi:10.1016/j.autrev.2005.10.007 · Cited by 256 · see citing works

Prenatal or early postnatal events predict infectious deaths in young adulthood in rural Africa

Moore, S. E. (1999) · International Journal of Epidemiology · doi:10.1093/ije/28.6.1088 · Cited by 255 · see citing works

Systematic Review: The Role of Breastfeeding in the Development of Pediatric Inflammatory Bowel Disease

Barclay, A. R., Russell, R. K., Wilson, M. L., Gilmour, W. H., Satsangi, J., & Wilson, D. C. (2009) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2009.03.017 · Cited by 249 · see citing works

Regulation of T Cell Responses in the Developing Human Fetus

Michaëlsson, J., Mold, J. E., McCune, J. M., & Nixon, D. F. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.176.10.5741 · Cited by 249 · see citing works

B-1 B Cell Development

Hardy, R. R. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.5.2749 · Cited by 249 · see citing works

Prebiotic oligosaccharides: In vitro evidence for gastrointestinal epithelial transfer and immunomodulatory properties

Eiwegger, T., Stahl, B., Haidl, P., Schmitt, J., Boehm, G., Dehlink, E., Urbanek, R., & Szépfalusi, Z. (2010) · Pediatric Allergy and Immunology · doi:10.1111/j.1399-3038.2010.01062.x · Cited by 246 · see citing works

Hematological Values of 163 Normal Fetuses between 18 and 30 Weeks of Gestation

Forestier, F., Daffos, F., Galactéros, F., Bardakjian, J., Rainaut, M., & Beuzard, Y. (1986) · Pediatric Research · doi:10.1203/00006450-198604000-00017 · Cited by 243 · see citing works

Effects of intrauterine growth retardation on mortality and morbidity in infants and young children.

Ashworth, A. (1998) · PubMed · Cited by 240 · see citing works

The regional pattern of retinoic acid synthesis by RALDH2 is essential for the development of posterior pharyngeal arches and the enteric nervous system

Niederreither, K., Vermot, J., Roux, I. L., Schuhbaur, B., Chambon, P., & Dollé, P. (2003) · Development · doi:10.1242/dev.00463 · Cited by 238 · see citing works

Breastfeeding protects against infectious diseases during infancy in industrialized countries. A systematic review

Duijts, L., Ramadhani, M. K., & Moll, H. A. (2009) · Maternal and Child Nutrition · doi:10.1111/j.1740-8709.2008.00176.x · Cited by 236 · see citing works

Role of infant feeding practices in development of Crohn's disease in childhood.

Koletzko, S., Sherman, P. M., Corey, M. L., Griffiths, A. M., & Smith, C. (1989) · BMJ · doi:10.1136/bmj.298.6688.1617 · Cited by 236 · see citing works

CCL28 Controls Immunoglobulin (Ig)A Plasma Cell Accumulation in the Lactating Mammary Gland and IgA Antibody Transfer to the Neonate

Wilson, E., & Butcher, E. C. (2004) · The Journal of Experimental Medicine · doi:10.1084/jem.20041069 · Cited by 229 · see citing works

Comparative trial in infants of four conjugate Haemophilus influenzae type b vaccines

Decker, M. D., Edwards, K. M., Bradley, R., & Palmer, P. S. (1992) · The Journal of Pediatrics · doi:10.1016/s0022-3476(05)80424-x · Cited by 228 · see citing works

Composition of Colostrum from Dairy Heifers Exposed to High Air Temperatures During Late Pregnancy and the Early Postpartum Period

Nardone, A., Lacetera, N., Bernabucci, U., & Ronchi, B. (1997) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(97)76005-3 · Cited by 228 · see citing works

Effect of early infant feeding practices on infection-specific neonatal mortality: an investigation of the causal links with observational data from rural Ghana

Edmond, K. M., Kirkwood, B. R., Amenga‐Etego, S., Owusu‐Agyei, S., & Hurt, L. S. (2007) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/86.4.1126 · Cited by 223 · see citing works

Inhibition of NF-κB and Oxidative Pathways in Human Dendritic Cells by Antioxidative Vitamins Generates Regulatory T Cells

Tan, P., Sagoo, P., Chan, C. C. W., Yates, J., Campbell, J., Beutelspacher, S. C., Foxwell, B. M. J., Lombardi, G., & George, A. J. T. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.12.7633 · Cited by 220 · see citing works

Gestational Zinc Deprivation in Mice: Persistence of Immunodeficiency for Three Generations

Beach, R. S., Gershwin, M. E., & Hurley, L. S. (1982) · Science · doi:10.1126/science.7123244 · Cited by 219 · see citing works

Retinoid signaling is essential for patterning the endoderm of the third and fourth pharyngeal arches

Wendling, O., Dennefeld, C., Chambon, P., & Mark, M. P. (2000) · Development · doi:10.1242/dev.127.8.1553 · Cited by 218 · see citing works

INFANT FEEDING AND CHILDHOOD CANCER

Davis, M., Savitz, D., & Graubard, B. I. (1988) · The Lancet · doi:10.1016/s0140-6736(88)92835-8 · Cited by 216 · see citing works

Decreased Mononuclear and Polymorphonuclear Chemotaxis in Human Newborns,Infants, and Young Children

Klein, R. B., Fischer, T. J., Gard, S. E., Biberstein, M., RICH, K. C., & Stiehm, E. R. (1977) · PEDIATRICS · doi:10.1542/peds.60.4.467 · Cited by 210 · see citing works

AN ASSOCIATION BETWEEN ABO BLOOD-GROUP DISTRIBUTION AND GEOGRAPHICAL DIFFERENCES IN DEATH-RATES

Mitchell, J. R. A. (1977) · The Lancet · doi:10.1016/s0140-6736(77)91838-4 · Cited by 209 · see citing works

The J Chain Is Essential for Polymeric Ig Receptor-Mediated Epithelial Transport of IgA

Johansen, F., Braathen, R., & Brandtzæg, P. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.167.9.5185 · Cited by 206 · see citing works

Cytokines in Human Milk

Garofalo, R. P. (2010) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2009.11.019 · Cited by 205 · see citing works

The Impact of Vitamin D on Regulatory T Cells

Chambers, E. S., & Hawrylowicz, C. M. (2010) · Current Allergy and Asthma Reports · doi:10.1007/s11882-010-0161-8 · Cited by 205 · see citing works

Maternal antioxidant intake in pregnancy and wheezing illnesses in children at 2 y of age

Litonjua, A. A., Rifas‐Shiman, S. L., Ly, N. P., Tantisira, K. G., Rich-Edwards, J. W., Camargo, C. A., Weiss, S. T., Gillman, M. W., & Gold, D. R. (2006) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/84.4.903 · Cited by 204 · see citing works

Late dominance of the inflammatory process in murine influenza by gamma/delta + T cells.

Carding, S. R., Allan, W., Kyes, S. A., Hayday, A., Bottomly, K., & Doherty, P. C. (1990) · The Journal of Experimental Medicine · doi:10.1084/jem.172.4.1225 · Cited by 204 · see citing works

Infant sex predicts breast milk energy content

Powe, C. E., Knott, C. D., & Conklin‐Brittain, N. L. (2009) · American Journal of Human Biology · doi:10.1002/ajhb.20941 · Cited by 200 · see citing works

Effects of maternal micronutrient supplementation on fetal loss and infant mortality: a cluster-randomized trial in Nepal

Christian, P. S., West, K. P., Khatry, S. K., LeClerq, S. C., Pradhan, E. K., Katz, J., Shrestha, S. R., & Sommer, A. H. (2003) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/78.6.1194 · Cited by 197 · see citing works

Endocrine and metabolic programming during intrauterine development

Fowden, A. L., Giussani, D. A., & Forhead, A. J. (2005) · Early Human Development · doi:10.1016/j.earlhumdev.2005.06.007 · Cited by 196 · see citing works

Early nutrition and the development of immune function in the neonate

Kelly, D., & Coutts, A. (2000) · Proceedings of The Nutrition Society · doi:10.1017/s0029665100000197 · Cited by 193 · see citing works

Uteroplacental vascular development and placental function: an update

Reynolds, L. P., Borowicz, P. P., Caton, J. S. S., Vonnahme, K. A., Luther, J. S., Buchanan, D. S., Hafez, S. A., Grazul‐Bilska, A. T., & Redmer, D. A. (2009) · The International Journal of Developmental Biology · doi:10.1387/ijdb.082799lr · Cited by 191 · see citing works

The maternal immune system's interaction with circulating fetal cells

Bonney, E. A., & Matzinger, P. (1997) · The Journal of Immunology · doi:10.4049/jimmunol.158.1.40 · Cited by 190 · see citing works

Placental antibody transfer: influence of maternal HIV infection and placental malaria

de Moraes-Pinto, M. I., Verhoeff, F., Chimsuku, L., Milligan, P. J. M., Wesumperuma, L., Broadhead, R. L., Brabin, B. J., Johnson, P. M., & Hart, C. A. (1998) · Archives of Disease in Childhood - Fetal and Neonatal Edition · doi:10.1136/fn.79.3.f202 · Cited by 189 · see citing works

Reduced risk of IDDM among breast-fed children. The Colorado IDDM Registry

Mayer, E. J., Hamman, R. F., Gay, E. C., Lezotte, D. C., Savitz, D. A., & KLINGENSMITH, G. J. (1988) · Diabetes · doi:10.2337/diabetes.37.12.1625 · Cited by 187 · see citing works

The thymus is a common target in malnutrition and infection

Savino, W., Dardenne, M., Velloso, L. A., & Silva-Barbosa, S. D. (2007) · British Journal Of Nutrition · doi:10.1017/s0007114507832880 · Cited by 185 · see citing works

Placental Transfer and Maternally Acquired Neonatal IgG Immunity in Human Immunodeficiency Virus Infection

de Moraes‐Pinto, M. I., de Almeida, A. C. M., Kenj, G., Filgueiras, T., Tobias, W., dos Santos, A. M. N., Carneiro-Sampaio, M. M. S., Farhat, C. K., Milligan, P. J., Johnson, P. M., et al. (1996) · The Journal of Infectious Diseases · doi:10.1093/infdis/173.5.1077 · Cited by 182 · see citing works

Antigen recognition by γδ T cells

Chien, Y., & Konigshofer, Y. (2007) · Immunological Reviews · doi:10.1111/j.1600-065x.2006.00470.x · Cited by 182 · see citing works

Silent mysteries: epigenetic paradigms could hold the key to conquering the epidemic of allergy and immune disease

Martino, D., & Prescott, S. L. (2009) · Allergy · doi:10.1111/j.1398-9995.2009.02186.x · Cited by 180 · see citing works

The development of gut associated lymphoid tissue in the terminal ileum of fetal human intestine.

Spencer, J., MacDonald, T. T., Finn, T., & Isaacson, P. G. (1986) · PubMed Central · Cited by 180 · see citing works

Oxidation‐specific epitopes are important targets of innate immunity

Chou, M. ‐., Hartvigsen, K., Hansen, L. F., Fogelstrand, L., Shaw, P. X., Boullier, A., Binder, C. J., & Witztum, J. L. (2008) · Journal of Internal Medicine · doi:10.1111/j.1365-2796.2008.01968.x · Cited by 179 · see citing works

Development and selection of γδ T cells

Xiong, N., & Raulet, D. H. (2007) · Immunological Reviews · doi:10.1111/j.1600-065x.2006.00478.x · Cited by 178 · see citing works

Abnormal mobility of neonatal polymorphonuclear leukocytes. Relationship to impaired redistribution of surface adhesion sites by chemotactic factor or colchicine.

Anderson, D. C., Hughes, B. J., & Smith, C. W. (1981) · Journal of Clinical Investigation · doi:10.1172/jci110341 · Cited by 174 · see citing works

A role for leptin in sustaining lymphopoiesis and myelopoiesis

Claycombe, K., King, L. E., & Fraker, P. J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0712053105 · Cited by 173 · see citing works

Prenatal undernutrition, postnatal environments, and antibody response to vaccination in adolescence

McDade, T. W., Beck, M. A., Kuzawa, C. W., & Adair, L. S. (2001) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/74.4.543 · Cited by 173 · see citing works

Development and activation of regulatory T cells in the human fetus

Cupedo, T., Nagasawa, M., Weijer, K. C., Blom, B., & Spits, H. (2005) · European Journal of Immunology · doi:10.1002/eji.200425763 · Cited by 171 · see citing works

Lysozyme, lactoferrin, and secretory immunoglobulin A content in breast milk: influence of duration of lactation, nutrition status, prolactin status, and parity of mother

Hennart, P., Brasseur, D., Delogne‐Desnoeck, J., Dramaix, M., & Robyn, C. (1991) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/53.1.32 · Cited by 169 · see citing works

Reduced risk of IDDM among breast-fed children. The Colorado IDDM Registry

Mayer, E. J., Hamman, R. F., Gay, E. C., Lezotte, D. C., Savitz, D. A., & Klingensmith, G. J. (1988) · Diabetes · doi:10.2337/diab.37.12.1625 · Cited by 169 · see citing works

Protein-Energy Malnutrition and Immunological Responses

Chandra, R. K. (1992) · Journal of Nutrition · doi:10.1093/jn/122.suppl_3.597 · Cited by 168 · see citing works

Micronutrients and Innate Immunity

Erickson, K. L., Medina, E. A., & Hubbard, N. E. (2000) · The Journal of Infectious Diseases · doi:10.1086/315922 · Cited by 167 · see citing works

Effects of prenatal stress on cellular and humoral immune responses in neonatal pigs

Tuchscherer, M., Kanitz, E., Otten, W., & Tuchscherer, A. (2002) · Veterinary Immunology and Immunopathology · doi:10.1016/s0165-2427(02)00035-1 · Cited by 165 · see citing works

Decreased embryonic retinoic acid synthesis results in a DiGeorge syndrome phenotype in newborn mice

Vermot, J., Niederreither, K., Garnier, J., Chambon, P., & Dollé, P. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0437920100 · Cited by 163 · see citing works

Maternal HIV infection and placental malaria reduce transplacental antibody transfer and tetanus antibody levels in newborns in Kenya

Cumberland, P., Shulman, C. E., Maple, P. A. C., Bulmer, J. N., Dorman, E. K., Kawuondo, K., Marsh, K., & Cutts, F. T. (2007) · The Journal of Infectious Diseases · doi:10.1086/519845 · Cited by 160 · see citing works

Placental Growth Throughout the Last Two Thirds of Pregnancy in Sheep: Vascular Development and Angiogenic Factor Expression1

Borowicz, P. P., Arnold, D. R., Johnson, M. L., Grazul-Bilska, A. T., Redmer, D. A., & Reynolds, L. P. (2007) · Biology of Reproduction · doi:10.1095/biolreprod.106.054684 · Cited by 160 · see citing works

Fetal B-cell lymphopoiesis and the emergence of B-1-cell potential

Dorshkind, K. A., & Montecino‐Rodriguez, E. (2007) · Nature reviews. Immunology · doi:10.1038/nri2019 · Cited by 159 · see citing works

Glycoproteins of the Human Milk Fat Globule in the Protection of the Breast-Fed Infant against Infections

Peterson, J. A., Patton, S., & Hamosh, M. (1998) · Neonatology · doi:10.1159/000014020 · Cited by 158 · see citing works

Chronic inflammation and mutagenesis

Ferguson, L. R. (2010) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2010.03.007 · Cited by 156 · see citing works

Trophic Effect of Multiple Growth Factors in Amniotic Fluid or Human Milk on Cultured Human Fetal Small Intestinal Cells

Hirai, C., Ichiba, H., Saito, M., Shintaku, H., Yamano, T., & Kusuda, S. (2002) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/00005176-200205000-00010 · Cited by 156 · see citing works

Functional analysis of neutrophil granulocytes from healthy, infected, and stressed neonates

Shigeoka, A. O., Santos, J. I., & Hill, H. R. (1979) · The Journal of Pediatrics · doi:10.1016/s0022-3476(79)80535-1 · Cited by 154 · see citing works

Low birth weight is associated with altered immune function in rural Bangladeshi children: a birth cohort study

Raqib, R., Alam, D. S., Sarker, P., Ahmad, S. M., Ara, G., Yunus, M., Moore, S. E., & Fuchs, G. J. (2007) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/85.3.845 · Cited by 152 · see citing works

The Need for Maternal Zinc Supplementation in Developing Countries: An Unresolved Issue

Osendarp, S. J. M., West, C. E., & Black, R. E. (2003) · The Journal of Nutrition · doi:10.1093/jn/133.3.817s · Cited by 152 · see citing works

ANTIMICROBIAL FACTORS IN HUMAN MILK

Reddy, V., Bhaskaram, C., Raghuramulu, N., & JAGADEESAN, V. (1977) · Acta Paediatrica · doi:10.1111/j.1651-2227.1977.tb07838.x · Cited by 150 · see citing works

Stress in obesity: Cause or consequence?

Foss, B., & Dyrstad, S. M. (2011) · Medical Hypotheses · doi:10.1016/j.mehy.2011.03.011 · Cited by 149 · see citing works

The epidermal barrier

Cartlidge, P. H. (2000) · Seminars in Neonatology · doi:10.1053/siny.2000.0013 · Cited by 144 · see citing works

Development and Basic Mechanisms of Human Gut Immunity

Brandtzæg, P. (2009) · Nutrition Reviews · doi:10.1111/j.1753-4887.1998.tb01645.x · Cited by 143 · see citing works

Effect of breast-feeding on antibody response to conjugate vaccine

Pabst, H., & Spady, D. (1990) · The Lancet · doi:10.1016/0140-6736(90)91802-h · Cited by 143 · see citing works

Long-Term Alterations in Neuroimmune Responses after Neonatal Exposure to Lipopolysaccharide

Lomax, L. B., Mouihate, A., Ellis, S. L., & Pittman, Q. J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1077-04.2004 · Cited by 142 · see citing works

Novel immunoregulatory functions of phenotypically distinct subpopulations of CD4+ cells in the human neonate.

Clement, L. T., Vink, P., & Bradley, G. E. (1990) · The Journal of Immunology · doi:10.4049/jimmunol.145.1.102 · Cited by 141 · see citing works

Zinc supplementation during pregnancy and effects on growth and morbidity in low birthweight infants: a randomsied placebo controlled trial

Osendarp, S. J. M., van Raaij, J. M., Darmstadt, G. L., Baqui, A. H., HAUTVAST, J. G. A. J., & Fuchs, G. J. (2001) · The Lancet · doi:10.1016/s0140-6736(00)04260-4 · Cited by 140 · see citing works

Decreased thymus size in formula‐fed infants compared with breastfed infants

Hasselbalch, H. C., Jeppesen, D. L., Engelmann, M., Michaelsen, K. F., & Nielsen, M. (1996) · Acta Paediatrica · doi:10.1111/j.1651-2227.1996.tb14211.x · Cited by 140 · see citing works

Prenatal Undernutrition and Postnatal Growth Are Associated with Adolescent Thymic Function

McDade, T. W., Beck, M. A., Kuzawa, C. W., & Adair, L. S. (2001) · Journal of Nutrition · doi:10.1093/jn/131.4.1225 · Cited by 138 · see citing works

Antibody Responses to Parenteral and Oral Vaccines Are Impaired by Conventional and Low Protein Formulas as Compared to Breast‐feeding

Hahn‐Zoric, M., Fulconis, F., MINOLI, I., MORO, G., Carlsson, B., Böttiger, M., RÄHÄ, N., & HANSON, L. Å. (1990) · Acta Paediatrica · doi:10.1111/j.1651-2227.1990.tb11401.x · Cited by 137 · see citing works

Protective function of human milk: The milk fat globule

Hamosh, M., Peterson, J. A., Henderson, T. R., Scallan, C. D., Kiwan, R., Ceriani, R., Armand, M., Mehta, N. R., & Hamosh, P. (1999) · Seminars in Perinatology · doi:10.1016/s0146-0005(99)80069-x · Cited by 136 · see citing works

Natural antibodies and the autoimmunity of atherosclerosis

Binder, C. J., & Silverman, G. J. (2004) · Springer Seminars in Immunopathology · doi:10.1007/s00281-004-0185-z · Cited by 136 · see citing works

Defining critical windows in the development of the human immune system

West, L. J. (2002) · Human & Experimental Toxicology · doi:10.1191/0960327102ht288oa · Cited by 135 · see citing works

Evolution of Immunologic Functions of the Mammary Gland and the Postnatal Development of Immunity

Goldman, A. S., Chheda, S., & Garofalo, R. P. (1998) · Pediatric Research · doi:10.1203/00006450-199802000-00001 · Cited by 134 · see citing works

Natural antibodies, intravenous immunoglobulin and their role in autoimmunity, cancer and inflammation

Schwartz‐Albiez, R., Monteiro, R. C., Rodriguez, M., Binder, C. J., & Shoenfeld, Y. (2009) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2009.04026.x · Cited by 133 · see citing works

Positive Selection of Anti–Thy-1 Autoreactive B-1 Cells and Natural Serum Autoantibody Production Independent from Bone Marrow B Cell Development

Hayakawa, K., Asano, M., Shinton, S. A., Gui, M., Wen, L., Brill‐Dashoff, J., & Hardy, R. R. (2003) · The Journal of Experimental Medicine · doi:10.1084/jem.20021459 · Cited by 132 · see citing works

Maternal low-dose vitamin A or β-carotene supplementation has no effect on fetal loss and early infant mortality: a randomized cluster trial in Nepal

Katz, J., West, K. P., Khatry, S. K., Pradhan, E. K., LeClerq, S. C., Christian, P. S., Wu, L. S., Adhikari, R., Shrestha, S. R., & Sommer, A. H. (2000) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/71.6.1570 · Cited by 127 · see citing works

Natural antibodies and cancer

Vollmers, H. P., & Brändlein, S. (2009) · New Biotechnology · doi:10.1016/j.nbt.2009.03.016 · Cited by 127 · see citing works

Reduced transfer of tetanus antibodies with placental malaria

Brair, M.-E., Brabin, B., Milligan, P., Maxwell, S., & Hart, C. A. (1994) · The Lancet · doi:10.1016/s0140-6736(94)90991-1 · Cited by 125 · see citing works

The influence of placental malaria infection and maternal hypergammaglobulinemia on transplacental transfer of antibodies and IgG subclasses in a rural West African population

Okoko, B. J., Wesumperuma, L. H., Ota, M. O. C., Pinder, M., Banya, W., Gomez, S. F., McAdam, K. P. J., & Hart, A. C. (2001) · The Journal of Infectious Diseases · doi:10.1086/322808 · Cited by 121 · see citing works

Retinoids and mammalian development.

Morriss-Kay, G., & Ward, S. (1999) · International Review of Cytology · doi:10.1016/s0074-7696(08)61566-1 · Cited by 120 · see citing works

Serum leptin concentrations during severe protein-energy malnutrition: Correlation with growth parameters and endocrine function

Soliman, A. T., Elzalabany, M. S., Salama, M., & Ansari, B. (2000) · Metabolism · doi:10.1053/meta.2000.6745 · Cited by 120 · see citing works

Long-term prevention of allergic diseases by using protein hydrolysate formula in at-risk infants

Mallet, E., & Hénocq, A. (1992) · The Journal of Pediatrics · doi:10.1016/s0022-3476(05)81415-5 · Cited by 119 · see citing works

Adult survival after prenatal exposure to the Dutch famine 1944–45

Roseboom, T. J., van der Meulen, J., Osmond, C., Barker, D. J. P., Ravelli, A. C. J., & Bleker, O. P. (2001) · Paediatric and Perinatal Epidemiology · doi:10.1046/j.1365-3016.2001.00336.x · Cited by 117 · see citing works

Role of early stress in the individual differences in host response to viral infection

Avitsur, R., Hunzeker, J., & Sheridan, J. F. (2005) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2005.09.006 · Cited by 115 · see citing works

Milk cytokines and subclinical breast inflammation in Tanzanian women: effects of dietary red palm oil or sunflower oil supplementation

Filteau, S., Lietz, Mulokozi, G., Bilotta, S., Henry, C. J., & Tomkins (1999) · Immunology · doi:10.1046/j.1365-2567.1999.00834.x · Cited by 113 · see citing works

Placental transfer and decay of maternally acquired antimeasles antibodies in Nigerian children

HARTTER, H. K., OYEDELE, O. I., DIETZ, K., KREIS, S., HOFFMAN, J. P., & MULLER, C. P. (2000) · The Pediatric Infectious Disease Journal · doi:10.1097/00006454-200007000-00010 · Cited by 113 · see citing works

The maternal-neonatal neuro-immune interface: Are there long-term implications for inflammatory or stress-related disease?

Shanks, N., & Lightman, S. L. (2001) · Journal of Clinical Investigation · doi:10.1172/jci200114592 · Cited by 111 · see citing works

The maternal-neonatal neuro-immune interface: Are there long-term implications for inflammatory or stress-related disease?

Shanks, N. M., & Lightman, S. L. (2001) · Journal of Clinical Investigation · doi:10.1172/jci14592 · Cited by 111 · see citing works

Early-Life Immune Challenge: Defining a Critical Window for Effects on Adult Responses to Immune Challenge

Spencer, S. J., Martin, S. M., Mouihate, A., & Pittman, Q. J. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301004 · Cited by 110 · see citing works

Early life immune challenge alters innate immune responses to lipopolysaccharide: implications for host defense as adults

Ellis, S. L., Mouihate, A., & Pittman, Q. J. (2005) · The FASEB Journal · doi:10.1096/fj.04-3569fje · Cited by 110 · see citing works

Milk-Derived Transforming Growth Factor-β and the Infant Immune Response

Penttila, I. (2010) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2009.11.016 · Cited by 108 · see citing works

Prenatal Stress Diminishes the Cytokine Response of Leukocytes to Endotoxin Stimulation in Juvenile Rhesus Monkeys

Coe, C. L., Kramer, M., Kirschbaum, C., Netter, P., & Fuchs, E. (2002) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.87.2.8233 · Cited by 108 · see citing works

Distinct progenitors for B-1 and B-2 cells are present in adult mouse spleen

Ghosn, E., Sadate-Ngatchou, P. I., Yang, Y., Herzenberg, L. A., & Herzenberg, L. (2011) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.1019764108 · Cited by 108 · see citing works

Improved thymic function in exclusively breastfed infants is associated with higher interleukin 7 concentrations in their mothers' breast milk

N’Gom, P. T., Collinson, A. C., Pido-Lopez, J., Henson, S. M., Prentice, A. M., & Aspinall, R. (2004) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/80.3.722 · Cited by 108 · see citing works

Future health implications of prenatal and early-life vitamin D status

Lucas, R. M., Ponsonby, A., Pasco, J. A., & Morley, R. (2008) · Nutrition Reviews · doi:10.1111/j.1753-4887.2008.00126.x · Cited by 107 · see citing works

Maternal and fetal immune responses during pregnancy.

Sargent, I. L. (1993) · PubMed · Cited by 106 · see citing works

Breast-feeding influences thymic size in late infancy

Hasselbalch, H. C., Engelmann, M. D. M., Ersbøll, A. K., Jeppesen, D. L., & Fleischer-Michaelsen, K. (1999) · European Journal of Pediatrics · doi:10.1007/s004310051258 · Cited by 106 · see citing works

Effect of maternal nutritional status on immunological substances in human colostrum and milk

Miranda, R., Saravia, N., Ackerman, R., Murphy, N., Berman, S., & McMurray, D. (1983) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/37.4.632 · Cited by 106 · see citing works

Breast milk immune factors in Bangladeshi women supplemented postpartum with retinol or β-carotene

Filteau, S., Rice, A. L., Ball, J. J., Chakraborty, J., Stoltzfus, R. J., de Francisco, A., & Willumsen, J. F. (1999) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/69.5.953 · Cited by 104 · see citing works

Idiotype-anti-idiotype network. II. Activation of silent clones by treatment at birth with idiotypes is associated with the expansion of idiotype-specific helper T cells.

Rubinstein, L. J., Yeh, M., & Bona, C. A. (1982) · The Journal of Experimental Medicine · doi:10.1084/jem.156.2.506 · Cited by 104 · see citing works

Differential modulation of the immune response by breast‐ or formula‐feeding of infants

Pabst, H. F., Spady, D. W., Pilarski, L., Mm, C., Beeler, J., & Krezolek, M. P. (1997) · Acta Paediatrica · doi:10.1111/j.1651-2227.1997.tb14900.x · Cited by 104 · see citing works

Decreased Levels of Embryonic Retinoic Acid Synthesis Accelerate Recovery From Arterial Growth Delay in a Mouse Model of DiGeorge Syndrome

Ryckebüsch, L., Bertrand, N., Mesbah, K., Bajolle, F., Niederreither, K., Kelly, R. G., & Zaffran, S. (2010) · Circulation Research · doi:10.1161/circresaha.109.205732 · Cited by 103 · see citing works

Neonatal treatment with low doses of anti-idiotypic antibody leads to the expression of a silent clone.

Hiernaux, J. R., Bona, C., & Baker, P. J. (1981) · The Journal of Experimental Medicine · doi:10.1084/jem.153.4.1004 · Cited by 102 · see citing works

Mechanisms of the hygiene hypothesis — molecular and otherwise

Vercelli, D. (2006) · Current Opinion in Immunology · doi:10.1016/j.coi.2006.09.002 · Cited by 101 · see citing works

Appearance of secretory IgM and IgA antibodies to Escherichia coli in saliva during early infancy and childhood

Mellander, L., Carlsson, B., & Hanson, L. Å. (1984) · The Journal of Pediatrics · doi:10.1016/s0022-3476(84)80548-x · Cited by 101 · see citing works

High Maternal HIV-1 Viral Load During Pregnancy Is Associated With Reduced Placental Transfer of Measles IgG Antibody

Farquhar, C., Nduati, R. W., Haigwood, N. L., Sutton, W. F., Mbori‐Ngacha, D., Richardson, B. A., & John-Stewart, G. C. (2005) · JAIDS Journal of Acquired Immune Deficiency Syndromes · doi:10.1097/01.qai.0000168179.68781.95 · Cited by 100 · see citing works

Immunoglobulins in Piglets from Sows Heat-Stressed Prepartum

Machado-Neto, R., Graves, C. N., & Curtis, S. E. (1987) · Journal of Animal Science · doi:10.2527/jas1987.652445x · Cited by 100 · see citing works

The Role of Corticosterone in the Loss in Immune Function in the Zinc-Deficient A/J Mouse

DePasquale-Jardieu, P., & Fraker, P. J. (1979) · Journal of Nutrition · doi:10.1093/jn/109.11.1847 · Cited by 98 · see citing works

Further characterization of the role of corticosterone in the loss of humoral immunity in zinc-deficient A/J mice as determined by adrenalectomy.

DePasquale-Jardieu, P., & Fraker, P. J. (1980) · The Journal of Immunology · doi:10.4049/jimmunol.124.6.2650 · Cited by 98 · see citing works

The thymus: a barometer of malnutrition

Prentice, A. M. (1999) · British Journal Of Nutrition · doi:10.1017/s0007114599000628 · Cited by 98 · see citing works

Maternal Night Blindness Increases Risk of Mortality in the First 6 Months of Life among Infants in Nepal

Christian, P. S., West, K. P., LeClerq, S. C., Kimbrough-Pradhan, E., Katz, J., Khatry, S. K., & Shrestha, S. R. (2001) · Journal of Nutrition · doi:10.1093/jn/131.5.1510 · Cited by 96 · see citing works

Early‐life nutritional and environmental determinants of thymic size in infants born in rural Bangladesh

Moore, S. E., Prentice, A. M., Wagatsuma, Y., Fulford, A. J., Collinson, A., Raqib, R., Vahter, M., Persson, L. Å., & Arifeen, S. E. (2009) · Acta Paediatrica · doi:10.1111/j.1651-2227.2009.01292.x · Cited by 95 · see citing works

The Intestinal Microbiome in Early Life: Health and Disease

Arrieta, M.-C., Stiemsma, L. T., Amenyogbe, N., Brown, E. M., & Finlay, B. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00427 · Cited by 1,024 · see citing works

Immune Dysfunction as a Cause and Consequence of Malnutrition

Bourke, C. D., Berkley, J. A., & Prendergast, A. J. (2016) · Trends in Immunology · doi:10.1016/j.it.2016.04.003 · Cited by 732 · see citing works

Immune responses in neonates

Basha, S., Surendran, N., & Pichichero, M. (2014) · Expert Review of Clinical Immunology · doi:10.1586/1744666x.2014.942288 · Cited by 513 · see citing works

How nutrition and the maternal microbiota shape the neonatal immune system

Macpherson, A. J., de Agüero, M. G., & Ganal-Vonarburg, S. C. (2017) · Nature Reviews Immunology · doi:10.1038/nri.2017.58 · Cited by 378 · see citing works

Impact of Childhood Malnutrition on Host Defense and Infection

Ibrahim, M. K., Zambruni, M., Melby, C. L., & Melby, P. C. (2017) · Clinical Microbiology Reviews · doi:10.1128/cmr.00119-16 · Cited by 359 · see citing works

Mechanisms underlying the effects of prenatal psychosocial stress on child outcomes: beyond the HPA axis

Beijers, R., Buitelaar, J. K., & de Weerth, C. (2014) · European Child & Adolescent Psychiatry · doi:10.1007/s00787-014-0566-3 · Cited by 321 · see citing works

A metagenomic study of diet-dependent interaction between gut microbiota and host in infants reveals differences in immune response

Schwartz, S., Friedberg, I., Ivanov, I. V., Davidson, L. A., Goldsby, J. S., Dahl, D. B., Herman, D., Wang, M., Donovan, S. M., & Chapkin, R. S. (2012) · Genome biology · doi:10.1186/gb-2012-13-4-r32 · Cited by 261 · see citing works

The influence of maternal prenatal and early childhood nutrition and maternal prenatal stress on offspring immune system development and neurodevelopmental disorders

Marques, A. H., O'Connor, T. G., Roth, C., Susser, E., & Bjørke-Monsen, A.-L. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00120 · Cited by 226 · see citing works

The role of environmental factors in modulating immune responses in early life

MacGillivray, D. M., & Kollmann, T. R. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00434 · Cited by 219 · see citing works

Factors Affecting the FcRn-Mediated Transplacental Transfer of Antibodies and Implications for Vaccination in Pregnancy

Wilcox, C. R., Holder, B., & Jones, C. E. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01294 · Cited by 200 · see citing works

Impact of Early-Life Exposures on Immune Maturation and Susceptibility to Disease

Gollwitzer, E. S., & Marsland, B. J. (2015) · Trends in Immunology · doi:10.1016/j.it.2015.09.009 · Cited by 205 · see citing works

Effect of Maternal Multiple Micronutrient vs Iron–Folic Acid Supplementation on Infant Mortality and Adverse Birth Outcomes in Rural Bangladesh

West, K. P., Shamim, A. A., Mehra, S., Labrique, A. B., Ali, H., Shaikh, S., Klemm, R. D. W., Wu, L. S.-F., Mitra, M., Haque, R., et al. (2014) · JAMA · doi:10.1001/jama.2014.16819 · Cited by 178 · see citing works

Perfluoroalkyl substances exposure and immunity, allergic response, infection, and asthma in children: Review of epidemiologic studies

von Holst, H., Nayak, P., Dembek, Z., Buehler, S., Echeverria, D., Fallacara, D., & John, L. (2021) · Heliyon · doi:10.1016/j.heliyon.2021.e08160 · Cited by 167 · see citing works

Maternal stress, nutrition and physical activity: Impact on immune function, CNS development and psychopathology

Marques, A. H., Bjørke-Monsen, A.-L., Teixeira, A. L., & Silverman, M. N. (2015) · Brain Research · doi:10.1016/j.brainres.2014.10.051 · Cited by 166 · see citing works

Development of immunity in early life

Goenka, A., & Kollmann, T. R. (2015) · Journal of Infection · doi:10.1016/j.jinf.2015.04.027 · Cited by 136 · see citing works

Influence of nutrient-derived metabolites on lymphocyte immunity

Veldhoen, M., & Ferreira, C. (2015) · Nature Medicine · doi:10.1038/nm.3894 · Cited by 125 · see citing works

The different effects of LPS and poly I:C prenatal immune challenges on the behavior, development and inflammatory responses in pregnant mice and their offspring

Arsenault, D., St-Amour, I., Cisbani, G., Rousseau, L.-S., & Cicchetti, F. (2014) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2013.12.016 · Cited by 118 · see citing works

Host-Microbe Interactions in the Neonatal Intestine: Role of Human Milk Oligosaccharides

Donovan, S. M., Wang, M., Li, M., Friedberg, I., Schwartz, S., & Chapkin, R. S. (2012) · Advances in Nutrition · doi:10.3945/an.112.001859 · Cited by 107 · see citing works

Stress, sex, and plague: Patterns of developmental stress and survival in pre‐ and post‐Black Death London

DeWitte, S. N. (2017) · American Journal of Human Biology · doi:10.1002/ajhb.23073 · Cited by 97 · see citing works

The Impact of Milk and Its Components on Epigenetic Programming of Immune Function in Early Life and Beyond: Implications for Allergy and Asthma

van Esch, B. C. A. M., Porbahaie, M., Abbring, S., Garssen, J., Potaczek, D. P., Savelkoul, H. F. J., & van Neerven, R. J. J. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.02141 · Cited by 97 · see citing works

Maternal Dietary Diversity Decreases with Household Food Insecurity in Rural Bangladesh: A Longitudinal Analysis

Na, M., Mehra, S., Christian, P. S., Ali, H., Shaikh, S., Shamim, A. A., Labrique, A. B., Klemm, R. D. W., Wu, L. S. F., & West, K. P. (2016) · Journal of Nutrition · doi:10.3945/jn.116.234229 · Cited by 96 · see citing works

Long-term activation of the innate immune system in atherosclerosis

Christ, A., Bekkering, S., Latz, E., & Riksen, N. P. (2016) · Seminars in Immunology · doi:10.1016/j.smim.2016.04.004 · Cited by 94 · see citing works

The interplay of early-life stress, nutrition, and immune activation programs adult hippocampal structure and function

Hoeijmakers, L., Lucassen, P. J., & Kőrösi, A. (2015) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2014.00103 · Cited by 92 · see citing works

Interaction of Nutrition and Infections Globally: An Overview

Krawinkel, M. B. (2012) · Annals of Nutrition and Metabolism · doi:10.1159/000345162 · Cited by 84 · see citing works

Maternal dietary diversity and dietary quality scores in relation to adverse birth outcomes in Tanzanian women

Madzorera, I., Isanaka, S., Wang, M., Msamanga, G., Urassa, W. K., Hertzmark, E., Duggan, C., & Fawzi, W. W. (2020) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/nqaa172 · Cited by 86 · see citing works

Prenatal stress effects in a wild, long-lived primate: predictive adaptive responses in an unpredictable environment

Berghänel, A., Heistermann, M., Schülke, O., & Ostner, J. (2016) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2016.1304 · Cited by 81 · see citing works

Nutritional control of immunity: Balancing the metabolic requirements with an appropriate immune function

Rosa, V. D., Galgani, M., Santopaolo, M., Colamatteo, A., Laccetti, R., & Matarese, G. (2015) · Seminars in Immunology · doi:10.1016/j.smim.2015.10.001 · Cited by 75 · see citing works

Twenty‐first century bioarchaeology: Taking stock and moving forward

Buikstra, J. E., DeWitte, S. N., Agarwal, S. C., Baker, B. J., Bartelink, E. J., Berger, E., Blevins, K. E., Bolhofner, K. L., Boutin, A. T., Brickley, M. B., et al. (2022) · American Journal of Biological Anthropology · doi:10.1002/ajpa.24494 · Cited by 66 · see citing works

Seasonal immune modulation in humans: Observed patterns and potential environmental drivers

Paynter, S., Ware, R. S., Sly, P. D., Williams, G. M., & Weinstein, P. (2014) · Journal of Infection · doi:10.1016/j.jinf.2014.09.006 · Cited by 57 · see citing works

Nutrition during pregnancy and early development (NuPED) in urban South Africa: a study protocol for a prospective cohort

Symington, E. A., Baumgartner, J., Malan, L., Zandberg, L., Ricci, C., & Smuts, C. M. (2018) · BMC Pregnancy and Childbirth · doi:10.1186/s12884-018-1943-6 · Cited by 57 · see citing works

Perinatal inflammation and adult psychopathology: From preclinical models to humans

Depino, A. M. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.09.010 · Cited by 54 · see citing works

Influence of iron status on risk of maternal or neonatal infection and on neonatal mortality with an emphasis on developing countries

Brabin, L., Brabin, B. J., & Gies, S. (2013) · Nutrition Reviews · doi:10.1111/nure.12049 · Cited by 54 · see citing works

They are what you eat: Can nutritional factors during gestation and early infancy modulate the neonatal immune response?

Prentice, S. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01641 · Cited by 52 · see citing works

The Nasopharyngeal, Ruminal, and Vaginal Microbiota and the Core Taxa Shared across These Microbiomes in Virgin Yearling Heifers Exposed to Divergent In Utero Nutrition during Their First Trimester of Gestation and in Pregnant Beef Heifers in Response to Mineral Supplementation

Amat, S., Holman, D. B., Schmidt, K. N., Menezes, A. C. B., Baumgaertner, F., Winders, T., Kirsch, J. D., Liu, T., Schwinghamer, T. D., Sedivec, K. K. K., et al. (2021) · Microorganisms · doi:10.3390/microorganisms9102011 · Cited by 51 · see citing works

Pregnancy, embryo-fetal development and nutrition: physiology around fetal programming

Musumeci, G., Castrogiovanni, P., Trovato, F. M., Parenti, R., Szychlinska, M. A., & Imbesi, R. (2015) · Journal of Histology and Histopathology · doi:10.7243/2055-091x-2-1 · Cited by 50 · see citing works

Prebiotic Supplementation During Pregnancy Modifies the Gut Microbiota and Increases Metabolites in Amniotic Fluid, Driving a Tolerogenic Environment In Utero

Brosseau, C., Selle, A., Duval, A., Misme‐Aucouturier, B., Chesneau, M., Brouard, S., Cherbuy, C., Cariou, V., Bouchaud, G., Mincham, K. T., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.712614 · Cited by 50 · see citing works

Fetal-Derived Immune Cells at the Roots of Lifelong Pathophysiology

Mass, E., & Gentek, R. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.648313 · Cited by 47 · see citing works

Perinatal inflammation: a common factor in the early origins of cardiovascular disease?

Nguyen, M. U., Wallace, M. J., Pepe, S., Menheniott, T. R., Moss, T. J. M., & Burgner, D. P. (2015) · Clinical Science · doi:10.1042/cs20150045 · Cited by 48 · see citing works

Iron Promotes Intestinal Development in Neonatal Piglets

Pu, Y., Li, S., Xiong, H., Zhang, X., Wang, Y., & Du, H. (2018) · Nutrients · doi:10.3390/nu10060726 · Cited by 45 · see citing works

Maternal Selenium and Developmental Programming

Pappas, A. C., Zoidis, E., & Chadio, S. E. (2019) · Antioxidants · doi:10.3390/antiox8050145 · Cited by 44 · see citing works

A case–control study of sporadic retinoblastoma in relation to maternal health conditions and reproductive factors: a report from the Children’s Oncology group

Heck, J. E., Omidakhsh, N., Azary, S., Ritz, B. R., Ehrenstein, O. S. V., Bunin, G. R., & Ganguly, A. A. (2015) · BMC Cancer · doi:10.1186/s12885-015-1773-0 · Cited by 43 · see citing works

Prenatal iron exposure and childhood type 1 diabetes

Størdal, K., McArdle, H. J., Hayes, H. E., Tapia, G., Viken, M. K., Lund‐Blix, N. A., Haugen, M. A., Joner, G., Skrivarhaug, T., Mårild, K., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-27391-4 · Cited by 43 · see citing works

Undernutrition and malaria in pregnancy – a dangerous dyad?

Unger, H. W., Ashorn, P., Cates, J., Dewey, K. G., & Rogerson, S. J. (2016) · BMC Medicine · doi:10.1186/s12916-016-0695-2 · Cited by 43 · see citing works

Developmental Origins of Health and Disease

Geddes, D. T., & Prescott, S. L. (2013) · Journal of Human Lactation · doi:10.1177/0890334412474371 · Cited by 40 · see citing works

Inflammatory Response in Preterm and Very Preterm Newborns with Sepsis

Segura-Cervantes, E., Mancilla-Ramı́rez, J., González‐Canudas, J., Alba, E., Santillán, R., Morales-Barquet, D. A., Sandoval‐Plata, G., & Galindo-Sevilla, N. (2016) · Mediators of Inflammation · doi:10.1155/2016/6740827 · Cited by 39 · see citing works

The Effect of Nutritional Elements on the Immune System

Karacabey, K. (2012) · Journal of Obesity & Weight loss Therapy · doi:10.4172/2165-7904.1000152 · Cited by 39 · see citing works

Developmental origin and sex-specific risk for infections and immune diseases later in life

Zazara, D. E., & Arck, P. (2018) · Seminars in Immunopathology · doi:10.1007/s00281-018-0713-x · Cited by 39 · see citing works

A Co-expression Analysis of the Placental Transcriptome in Association With Maternal Pre-pregnancy BMI and Newborn Birth Weight

Cox, B., Tsamou, M., Vrijens, K., Neven, K. Y., Winckelmans, E., de Kok, T. M. C. M., Plusquin, M., & Nawrot, T. S. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.00354 · Cited by 37 · see citing works

Air pollution from traffic during pregnancy impairs newborn's cord blood immune cells: The NELA cohort

García‐Serna, A. M., Hernández‐Caselles, T., Jiménez‐Guerrero, P., Martín‐Orozco, E., Pérez‐Fernández, V., Cantero‐Cano, E., Muñoz‐García, M., Meseguer, C. B., Cobos, I. P. D. L., García‐Marcos, L., et al. (2020) · Environmental Research · doi:10.1016/j.envres.2020.110468 · Cited by 37 · see citing works

Effects of prenatal stress on hypothalamic–pituitary–adrenal (HPA) axis function over two generations of guinea pigs (Cavia aperea f. porcellus)

Schöpper, H., Palme, R., Ruf, T., & Huber, S. (2011) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2011.12.010 · Cited by 36 · see citing works

Early Life Factors Associated with Adult-Onset Systemic Lupus Erythematosus in Women

Parks, C. G., D’Aloisio, A. A., & Sandler, D. P. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00103 · Cited by 36 · see citing works

Immunoendocrinology: Faulty hormonal imprinting in the immune system

Csaba, G. (2014) · Acta Microbiologica et Immunologica Hungarica · doi:10.1556/amicr.61.2014.2.1 · Cited by 34 · see citing works

Impact of nutritional supplementation during pregnancy on antibody responses to diphtheria-tetanus-pertussis vaccination in infants: A randomised trial in The Gambia

Okala, S., Darboe, M. K., Sosseh, F., Sonko, B. J., Faye‐Joof, T., Prentice, A. M., & Moore, S. E. (2019) · PLoS Medicine · doi:10.1371/journal.pmed.1002854 · Cited by 34 · see citing works

Failure to Thrive in the Outpatient Clinic: A New Insight

Lezo, A., Baldini, L., & Asteggiano, M. (2020) · Nutrients · doi:10.3390/nu12082202 · Cited by 34 · see citing works

Prospects of nutritional interventions in the care of COVID-19 patients

Alam, S., Bhuiyan, F. R., Emon, T. H., & Hasan, M. (2021) · Heliyon · doi:10.1016/j.heliyon.2021.e06285 · Cited by 33 · see citing works

Reduced Poliovirus vaccine neutralising-antibody titres in infants with maternal HIV-exposure

Sanz-Ramos, M., Manno, D., Kapambwe, M., Ndumba, I., Musonda, K. G., Bates, M., Chibumbya, J. N., Siame, J., Monze, M., Filteau, S., et al. (2013) · Vaccine · doi:10.1016/j.vaccine.2013.02.044 · Cited by 34 · see citing works

Interactions of Nutrition and Infection: The Role of Micronutrient Deficiencies in the Immune Response to Pathogens and Implications for Child Health

Palmer, A., Bedsaul-Fryer, J. R., & Stephensen, C. B. (2024) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-062122-014910 · Cited by 39 · see citing works

Effect of Infant Formula Containing a Low Dose of the Probiotic Bifidobacterium lactis CNCM I-3446 on Immune and Gut Functions in C-Section Delivered Babies: A Pilot Study

Baglatzi, L., Gavrili, S., Stamouli, K., Zachaki, S., Favre, L., Pecquet, S., Benyacoub, J., & Costalos, C. (2016) · Clinical Medicine Insights Pediatrics · doi:10.4137/cmped.s33096 · Cited by 33 · see citing works

Ramadan Exposure In Utero and Child Mortality in Burkina Faso: Analysis of a Population-Based Cohort Including 41,025 Children

Schoeps, A., van Ewijk, R. J. G., Kynast‐Wolf, G., Nebie, E. I., Zabré, P., Sié, A., & Gabrysch, S. (2018) · American Journal of Epidemiology · doi:10.1093/aje/kwy091 · Cited by 33 · see citing works

Characterization of the Microbiota Associated With 12-Week-Old Bovine Fetuses Exposed to Divergent in utero Nutrition

Amat, S., Holman, D. B., Schmidt, K. N., McCarthy, K. L., Dorsam, S. T., Ward, A. K. K., Borowicz, P. P., Reynolds, L. P., Caton, J. S. S., Sedivec, K. K. K., et al. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.771832 · Cited by 32 · see citing works

The Effect of Human Immunodeficiency Virus and Cytomegalovirus Infection on Infant Responses to Vaccines: A Review

Falconer, O., Newell, M., & Jones, C. E. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00328 · Cited by 32 · see citing works

Pre-Weaning Growth Hormone Treatment Ameliorates Bone Marrow Macrophage Inflammation in Adult Male Rat Offspring following Maternal Undernutrition

Reynolds, C. M., Li, M., Gray, C. L., & Vickers, M. H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0068262 · Cited by 31 · see citing works

Maternal iron supplement intake during pregnancy and risk of celiac disease in children

Størdal, K., Haugen, M., Brantsæter, A., Lundin, K., & Stene, L. C. (2013) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2013.09.061 · Cited by 33 · see citing works

Childhood histoplasmosis in Colombia: Clinical and laboratory observations of 45 patients

López, L. F., Valencia, Y., Tobón, Á. M., Velásquez, Ó., Escobar, C. D. S., Caceres, D. H., Restrepo, Á., & Cano, L. E. (2016) · Medical Mycology · doi:10.1093/mmy/myw020 · Cited by 31 · see citing works

The “weanling's dilemma” revisited: Evolving bodies of evidence and the problem of infant paleodietary interpretation

Kendall, E. J., Millard, A. R., & Beaumont, J. (2021) · American Journal of Physical Anthropology · doi:10.1002/ajpa.24207 · Cited by 31 · see citing works

Preventing Atopic Diseases During Childhood – Early Exposure Matters

Pierau, M., Arra, A., & Brunner-Weinzierl, M. C. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.617731 · Cited by 32 · see citing works

Low Birth Weight and Risk of Progression to End Stage Renal Disease in IgA Nephropathy—A Retrospective Registry-Based Cohort Study

Ruggajo, P., Svarstad, E., Leh, S. M., Marti, H., Reisæter, A. V., & Vikse, B. E. (2016) · PLoS ONE · doi:10.1371/journal.pone.0153819 · Cited by 30 · see citing works

Mare's milk as a prospective functional product

Kushugulova, A. R., Kozhakhmetov, S., Sattybayeva, R., Nurgozhina, A., Ziyat, A., Yadav, H., & Marotta, F. (2018) · Functional Foods in Health and Disease · doi:10.31989/ffhd.v8i11.528 · Cited by 29 · see citing works

Sex-specific impact of prenatal stress on growth and reproductive parameters of guinea pigs

Schöpper, H., Klaus, T., Palme, R., Ruf, T., & Huber, S. (2012) · Journal of Comparative Physiology B · doi:10.1007/s00360-012-0680-9 · Cited by 28 · see citing works

Ontogeny of Mucosal Immunity and Aging

Gleeson, M., & Cripps, A. W. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-415847-4.00011-2 · Cited by 28 · see citing works

Whole-body microbiota of newborn calves and their response to prenatal vitamin and mineral supplementation

Luecke, S. M., Holman, D. B., Schmidt, K. N., Gzyl, K. E., Hurlbert, J. L., Menezes, A. C. B., Bochantin, K. A., Kirsch, J. D., Baumgaertner, F., Sedivec, K. K. K., et al. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1207601 · Cited by 27 · see citing works

The intrauterine origins of Hodgkin's lymphoma

Barker, D. J., Osmond, C., Thornburg, K. L. R., Kajantie, E., & Eriksson, J. G. (2013) · Cancer Epidemiology · doi:10.1016/j.canep.2013.01.004 · Cited by 27 · see citing works

Maternal Dietary Restriction During the Periconceptional Period in Normal-Weight or Obese Ewes Results in Adrenocortical Hypertrophy, an Up-Regulation of the JAK/STAT and Down-Regulation of the IGF1R Signaling Pathways in the Adrenal of the Postnatal Lamb

Zhang, S., Morrison, J. L., Gill, A., Rattanatray, L., MacLaughlin, S. M., Kleemann, D. O., Walker, S. K., & McMillen, I. C. (2013) · Endocrinology · doi:10.1210/en.2013-1414 · Cited by 27 · see citing works

Bovine Animal Model for Studying the Maternal Microbiome, in utero Microbial Colonization and Their Role in Offspring Development and Fetal Programming

Amat, S., Dahlen, C. R., Swanson, K. C., Ward, A. K. K., Reynolds, L. P., & Caton, J. S. S. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.854453 · Cited by 28 · see citing works

Immunity and ultrasonic vocalization in rodents

Jouda, J., Wöhr, M., & del Rey, A. (2018) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13931 · Cited by 25 · see citing works

Maternal vitamin A supplementation increases natural antibody concentrations of preadolescent offspring in rural Nepal

Palmer, A., Schulze, K. J., Khatry, S. K., Luca, L. M. D., & West, K. P. (2014) · Nutrition · doi:10.1016/j.nut.2014.11.016 · Cited by 25 · see citing works

The Role of Malnutrition during Pregnancy and Its Effects on Brain and Skeletal Muscle Postnatal Development

Castrogiovanni, P., & Imbesi, R. (2017) · Journal of Functional Morphology and Kinesiology · doi:10.3390/jfmk2030030 · Cited by 25 · see citing works

Childhood Residential and Agricultural Pesticide Exposures in Relation to Adult-Onset Rheumatoid Arthritis in Women

Parks, C. G., D’Aloisio, A. A., & Sandler, D. P. (2017) · American Journal of Epidemiology · doi:10.1093/aje/kwx224 · Cited by 25 · see citing works

Maternal diet quality before pregnancy and risk of childhood leukaemia

Singer, A. W., Carmichael, S. L., Selvin, S., Fu, C. H., Block, G., & Metayer, C. (2016) · British Journal Of Nutrition · doi:10.1017/s0007114516003469 · Cited by 24 · see citing works

Zinc homeostasis in immunity and its association with preterm births

Kumari, D., Garg, S., & Bhawrani, P. (2022) · Scandinavian Journal of Immunology · doi:10.1111/sji.13142 · Cited by 24 · see citing works

Abnormal immune system development and function in schizophrenia helps reconcile diverse findings and suggests new treatment and prevention strategies

Anders, S. L., & Kinney, D. K. (2015) · Brain Research · doi:10.1016/j.brainres.2015.02.043 · Cited by 25 · see citing works

Impact of In Utero Exposure to Malaria on Fetal T Cell Immunity

Odorizzi, P. M., & Feeney, M. E. (2016) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2016.08.005 · Cited by 24 · see citing works

Maternal cytokine status may prime the metabolic profile and increase risk of obesity in children

Englich, B., Herberth, G., Rolle-Kampczyk, U. E., Trump, S., Röder, S. W., Borte, M., Stangl, G. I., von Bergen�, M., Lehmann, I., & Junge, K. M. (2017) · International Journal of Obesity · doi:10.1038/ijo.2017.113 · Cited by 24 · see citing works

Unbiased Screening Identifies Functional Differences in NK Cells After Early Life Psychosocial Stress

Fernandes, S. B., Patil, N. D., Mériaux, S. B., Thérésine, M., Muller, C. P., Leenen, F. A. D., Elwenspoek, M. M. C., Zimmer, J., & Turner, J. D. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.674532 · Cited by 22 · see citing works

Immunogenicity of an oral rotavirus vaccine administered with prenatal nutritional support in Niger: A cluster randomized clinical trial

Isanaka, S., Garba, S., Plikaytis, B. D., McNeal, M., Guindo, O., Langendorf, C., Adehossi, E. O., Ciglenečki, I., & Grais, R. F. (2021) · PLoS Medicine · doi:10.1371/journal.pmed.1003720 · Cited by 23 · see citing works

Maternal diet and obesity shape offspring central and peripheral inflammatory outcomes in juvenile non-human primates

Dunn, G. A., Mitchell, A. J., Selby, M., Fair, D. A., Gustafsson, H., & Sullivan, E. L. (2022) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2022.02.024 · Cited by 23 · see citing works

Diet‐associated vertically transferred metabolites and risk of asthma, allergy, eczema, and infections in early childhood

Brustad, N., Olarini, A., Kim, M. G., Chen, L., Ali, M., Wang, T., Cohen, A. S., Ernst, M., HOUGAARD, D. M., Schoos, A. M., et al. (2023) · Pediatric Allergy and Immunology · doi:10.1111/pai.13917 · Cited by 22 · see citing works

Maternal use of dietary supplements during pregnancy is not associated with coeliac disease in the offspring: The Environmental Determinants of Diabetes in the Young (TEDDY) study

Yang, J., Tamura, R., Aronsson, C. A., Uusitalo, U. M., Lernmark, Å., Rewers, M., Hagopian, W., She, J., Toppari, J., Ziegler, A. G., et al. (2017) · British Journal Of Nutrition · doi:10.1017/s0007114517000332 · Cited by 22 · see citing works

Maternal Nutritional Status During Pregnancy and Infant Immune Response to Routine Childhood Vaccinations

Obanewa, O. A., & Newell, M. (2017) · Future Virology · doi:10.2217/fvl-2017-0021 · Cited by 22 · see citing works

The role of nutrition in immunity in infants and toddlers: An expert panel opinion

Pai, U., Chandrasekhar, P., Carvalho, R. S., & Kumar, S. A. (2017) · Clinical Epidemiology and Global Health · doi:10.1016/j.cegh.2017.11.004 · Cited by 22 · see citing works

Infection in the Developing Brain: The Role of Unique Systemic Immune Vulnerabilities

Singh, G., Tucker, E. W., & Rohlwink, U. K. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2021.805643 · Cited by 24 · see citing works

Choline is required in the diet of lactating dams to maintain maternal immune function

Dellschaft, N. S., Ruth, M. R., Goruk, S., Lewis, E. D., Richard, C., Jacobs, R. L., Curtis, J. M., & Field, C. J. (2015) · British Journal Of Nutrition · doi:10.1017/s0007114515001221 · Cited by 21 · see citing works

In vitroscreening of mare's milk antimicrobial effect and antiproliverative activity

Guri, A., Paligot, M., Crèvecoeur, S., Piedboeuf, B., Claes, J., Daube, G., Corredig, M., Griffiths, M. W., & Delcenserie, V. (2015) · FEMS Microbiology Letters · doi:10.1093/femsle/fnv234 · Cited by 20 · see citing works

Breast milk polyunsaturated fatty acids: associations with adolescent allergic disease and lung function

Waidyatillake, N. T., Stoney, R., Thien, F. C. K., Lodge, C., Simpson, J. A., Allen, K. J., Abramson, M. J., Erbas, B., Svanes, C., Dharmage, S. C., et al. (2016) · Allergy · doi:10.1111/all.13114 · Cited by 21 · see citing works

Vitamin D deficiency in pregnancy may affect fetal thymus development

Gür, E. B., Gür, M. S., İnce, Ö., Kasap, E., Genç, M., Tatar, S., Buğday, S., Turan, G. A., & Güçlü, S. (2016) · Ginekologia Polska · doi:10.5603/gp.2016.0008 · Cited by 20 · see citing works

Long-Term Outcomes of in Utero Ramadan Exposure: A Systematic Literature Review

Mahanani, M. R., Abderbwih, E., Wendt, A. S., Deckert, A., Antia, K., Horstick, O., Dambach, P., Kohler, S., & Winkler, V. F. (2021) · Nutrients · doi:10.3390/nu13124511 · Cited by 17 · see citing works

Maternal prenatal intake of one-carbon metabolism nutrients and risk of childhood leukemia

Singer, A. W., Selvin, S., Block, G., Golden, C. E. M., Carmichael, S. L., & Metayer, C. (2016) · Cancer Causes & Control · doi:10.1007/s10552-016-0773-y · Cited by 17 · see citing works

Prenatal maternal stress effects on the development of primate social behavior

Schülke, O., Ostner, J., & Berghänel, A. (2019) · Behavioral Ecology and Sociobiology · doi:10.1007/s00265-019-2729-1 · Cited by 17 · see citing works

Month of birth and cause-specific mortality between 50 and 80 years: a population-based longitudinal cohort study in Sweden

Ueda, P., Bonamy, A. E., Granath, F. N., & Cnattingius, S. (2014) · European Journal of Epidemiology · doi:10.1007/s10654-014-9882-7 · Cited by 16 · see citing works

Leukocytes in expressed breast milk of asthmatic mothers

Dixon, D., & Forsyth, K. D. (2016) · Allergologia et Immunopathologia · doi:10.1016/j.aller.2016.08.015 · Cited by 16 · see citing works

Maternal Nutrition and Fetal Programming of the Immune System: Epidemiological and Experimental Evidences

Ahmad, S. R. (2019) · Asian Journal of Medicine and Health · doi:10.9734/ajmah/2019/v14i330103 · Cited by 1 · see citing works

Editorial: Sustained Effects of Early Nutrition on Immune Development and Microbiome-Immune Crosstalk

Lewis, M. C., Childs, C. E., & Pérez-Cano, F. J. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01687 · Cited by 1 · see citing works

The role of specific maternal nutritional factors on epigenetic programming of fetal immune development

Amarasekera, M. (2015) · UWA Profiles and Research Repository (UWA)

Role of Maternal and Infant Malnutrition on the Development of the Inflammatory Response

Landgraf, M. A., Landgraf, R. G., & Fortes, Z. B. (2010) · Humana Press eBooks · doi:10.1007/978-1-60761-061-8_3 · Cited by 1 · see citing works

Nutritional Programming of Immune Defense Against Infections in Early Life

Nauta, A. J., & Garssen, J. (2014) · AAPS advances in the pharmaceutical sciences series · doi:10.1007/978-3-319-06151-1_7 · Cited by 7 · see citing works