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

An obesity-associated gut microbiome with increased capacity for energy harvest

Turnbaugh, P. J., Ley, R. E., Mahowald, M. A., Magrini, V., Mardis, E. R., & Gordon, J. I. (2006) · Nature · doi:10.1038/nature05414 · Cited by 12,444 · see citing works

Hay fever, hygiene, and household size.

Strachan, D. P. (1989) · BMJ · doi:10.1136/bmj.299.6710.1259 · Cited by 5,054 · see citing works

The gut microbiota shapes intestinal immune responses during health and disease

Round, J. L., & Mazmanian, S. K. (2009) · Nature Reviews Immunology · doi:10.1038/nri2515 · Cited by 5,029 · see citing works

Delivery mode shapes the acquisition and structure of the initial microbiota across multiple body habitats in newborns

Dominguez-Bello, M. G., Costello, E. K., Contreras, M., Magris, M., Hidalgo, G., Fierer, N., & Knight, R. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1002601107 · Cited by 4,774 · see citing works

Gut Microbiota from Twins Discordant for Obesity Modulate Metabolism in Mice

Ridaura, V. K., Faith, J. J., Rey, F. E., Cheng, J., Duncan, A. E., Kau, A. L., Griffin, N. W., Lombard, V., Henrissat, B., Bain, J. R., et al. (2013) · Science · doi:10.1126/science.1241214 · Cited by 3,788 · see citing works

Inflammatory Mechanisms in Obesity

Gregor, M. F., & Hotamisligil, G. S. (2011) · Annual Review of Immunology · doi:10.1146/annurev-immunol-031210-101322 · Cited by 3,754 · see citing works

Epigenetic modifications and human disease

Portela, A., & Esteller, M. (2010) · Nature Biotechnology · doi:10.1038/nbt.1685 · Cited by 2,843 · see citing works

Prevention of Allogeneic Fetal Rejection by Tryptophan Catabolism

Munn, D. H., Zhou, M., Attwood, J. T., Bondarev, I. E., Conway, S. J., Marshall, B., Brown, C. C., & Mellor, A. L. (1998) · Science · doi:10.1126/science.281.5380.1191 · Cited by 2,589 · see citing works

Hematopoiesis: An Evolving Paradigm for Stem Cell Biology

Orkin, S. H., & Zon, L. I. (2008) · Cell · doi:10.1016/j.cell.2008.01.025 · Cited by 2,570 · see citing works

Intrauterine infection and preterm delivery

Goldenberg, R. L., Hauth, J. C., & Andrews, W. W. (2000) · New England Journal of Medicine · doi:10.1056/nejm200005183422007 · Cited by 2,548 · see citing works

Environmental epigenomics and disease susceptibility

Jirtle, R. L., & Skinner, M. K. (2007) · Nature Reviews Genetics · doi:10.1038/nrg2045 · Cited by 2,492 · see citing works

Trained Immunity: A Memory for Innate Host Defense

Netea, M. G., Quintin, J., & van der Meer, J. W. M. (2011) · Cell Host & Microbe · doi:10.1016/j.chom.2011.04.006 · Cited by 1,697 · see citing works

Breastfeeding and Maternal and Infant Health Outcomes In Developed Countries

(2007) · AAP Grand Rounds · doi:10.1542/gr.18-2-15 · Cited by 1,540 · see citing works

Unravelling the effects of the environment and host genotype on the gut microbiome

Spor, A., Koren, O., & Ley, R. (2011) · Nature Reviews Microbiology · doi:10.1038/nrmicro2540 · Cited by 1,509 · see citing works

Breastfeeding and maternal and infant health outcomes in developed countries.

Ip, S., Chung, M. C., Raman, G., Chew, P., Magula, N. P., DeVine, D., Trikalinos, T. A., & Lau, J. (2007) · PubMed Central · Cited by 1,416 · see citing works

Variation in protection by BCG: implications of and for heterologous immunity

Fine, P. (1995) · The Lancet · doi:10.1016/s0140-6736(95)92348-9 · Cited by 1,385 · see citing works

Innate immunity of the newborn: basic mechanisms and clinical correlates

Levy, O. (2007) · Nature reviews. Immunology · doi:10.1038/nri2075 · Cited by 1,227 · see citing works

Gut Microbiomes of Malawian Twin Pairs Discordant for Kwashiorkor

Smith, M. I., Yatsunenko, T., Manary, M. J., Trehan, I., Mkakosya, R., Cheng, J., Kau, A. L., Rich, S. S., Concannon, P., Mychaleckyj, J. C., et al. (2013) · Science · doi:10.1126/science.1229000 · Cited by 1,173 · see citing works

The Dutch Famine and Its Long-Term Consequences for Adult Health

Roseboom, T., de Rooij, S., & Painter, R. (2006) · Early Human Development · doi:10.1016/j.earlhumdev.2006.07.001 · Cited by 1,137 · see citing works

Protection by BCG vaccine against tuberculosis: a systematic review of randomized controlled trials

Mangtani, P., Abubakar, I., Ariti, C., Beynon, R., Pimpin, L., Fine, P. E. M., Rodrigues, L. C., Smith, P. G., Lipman, M., Whiting, P. F., et al. (2014) · Clinical Infectious Diseases · doi:10.1093/cid/cit790 · Cited by 995 · see citing works

Developmental Origins of Health and Disease: Brief History of the Approach and Current Focus on Epigenetic Mechanisms

Wadhwa, P. D., Buß, C., Entringer, S., & Swanson, J. (2009) · Seminars in Reproductive Medicine · doi:10.1055/s-0029-1237424 · Cited by 986 · see citing works

Discovery of Human Zinc Deficiency: Its Impact on Human Health and Disease

Prasad, A. S. (2013) · Advances in Nutrition · doi:10.3945/an.112.003210 · Cited by 919 · see citing works

Cardiovascular and diabetes mortality determined by nutrition during parents' and grandparents' slow growth period

Kaati, G., Bygren, L., & Edvinsson, S. (2002) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5200859 · Cited by 896 · 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

Pregnancy and Infection

Kourtis, A. P., Read, J. S., & Jamieson, D. J. (2014) · New England Journal of Medicine · doi:10.1056/nejmra1213566 · Cited by 850 · see citing works

The human milk microbiota: Origin and potential roles in health and disease

Fernández, L., Langa, S., Martín, V., Maldonado‐Barragán, A., Jiménez, E., Martı́n, R., & Rodríguez, J. M. (2012) · Pharmacological Research · doi:10.1016/j.phrs.2012.09.001 · Cited by 849 · see citing works

Metagenomic systems biology of the human gut microbiome reveals topological shifts associated with obesity and inflammatory bowel disease

Greenblum, S., Turnbaugh, P. J., & Borenstein, E. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1116053109 · Cited by 821 · see citing works

Serum Vaccine Antibody Concentrations in Children Exposed to Perfluorinated Compounds

Grandjean, P., Andersen, E. W., Budtz-Jørgensen, E., Nielsen, F., Mølbak, K., Weihe, P., & Heilmann, C. (2012) · JAMA · doi:10.1001/jama.2011.2034 · Cited by 809 · see citing works

Developmental origins of non-communicable disease: Implications for research and public health

Barouki, R., Gluckman, P. D., Grandjean, P., Hanson, M. A., & Heindel, J. J. (2012) · Environmental Health · doi:10.1186/1476-069x-11-42 · Cited by 788 · see citing works

Prenatal exposure to the Dutch famine and disease in later life: An overview

Painter, R. C., Roseboom, T. J., & Bleker, O. P. (2005) · Reproductive Toxicology · doi:10.1016/j.reprotox.2005.04.005 · Cited by 784 · see citing works

‘ Everything is everywhere , but, the environment selects ’; what did Baas Becking and Beijerinck really say?

de Wit, R., & Bouvier, T. C. (2006) · Environmental Microbiology · doi:10.1111/j.1462-2920.2006.01017.x · Cited by 730 · see citing works

Pregnancy and pregnancy-associated hormones alter immune responses and disease pathogenesis

Robinson, D. P., & Klein, S. L. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2012.02.023 · Cited by 711 · see citing works

Isolation of Commensal Bacteria from Umbilical Cord Blood of Healthy Neonates Born by Cesarean Section

Jiménez, E., Fernández, L., Marín, M. L., Martı́n, R., Odriozola, J. M., Nueno‐Palop, C., Narbad, A., Olivares, M. M., Xaus, J., & Rodríguez, J. M. (2005) · Current Microbiology · doi:10.1007/s00284-005-0020-3 · Cited by 681 · see citing works

Interactions Between Gut Microbiota and Host Metabolism Predisposing to Obesity and Diabetes

Musso, G., Gambino, R., & Cassader, M. (2011) · Annual Review of Medicine · doi:10.1146/annurev-med-012510-175505 · Cited by 598 · see citing works

Mother's little helpers: mechanisms of maternal-fetal tolerance

Trowsdale, J., & Betz, A. G. (2006) · Nature Immunology · doi:10.1038/ni1317 · Cited by 576 · see citing works

Innate Immune Function by Toll-like Receptors: Distinct Responses in Newborns and the Elderly

Kollmann, T. R., Levy, O., Montgomery, R. R., & Goriely, S. (2012) · Immunity · doi:10.1016/j.immuni.2012.10.014 · Cited by 572 · see citing works

Lymphoid Potential, Probed before Circulation in Mouse, Is Restricted to Caudal Intraembryonic Splanchnopleura

Cumano, A., Dieterlen‐Lièvre, F., & Godin, I. (1996) · Cell · doi:10.1016/s0092-8674(00)80166-x · Cited by 567 · see citing works

Mercury Exposure and Children's Health

Böse‐O’Reilly, S., McCarty, K. M., Steckling, N., & Lettmeier, B. (2010) · Current problems in pediatric and adolescent health care · doi:10.1016/j.cppeds.2010.07.002 · Cited by 561 · see citing works

The Immunological Components of Human Milk and Their Effect on Immune Development in Infants ,

Field, C. J. (2005) · Journal of Nutrition · doi:10.1093/jn/135.1.1 · Cited by 555 · see citing works

The Lung Tissue Microbiome in Chronic Obstructive Pulmonary Disease

Sze, M. A., Dimitriu, P. A., Hayashi, S., Elliott, W. M., McDonough, J. E., Gosselink, J. V., Cooper, J. D., Sin, D. D., Mohn, W. W., & Hogg, J. C. (2012) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201111-2075oc · Cited by 552 · see citing works

Cesarean Versus Vaginal Delivery: Long-term Infant Outcomes and the Hygiene Hypothesis

Neu, J., & Rushing, J. (2011) · Clinics in Perinatology · doi:10.1016/j.clp.2011.03.008 · Cited by 528 · see citing works

Disease activity of rheumatoid arthritis during pregnancy: Results from a nationwide prospective study

de Man, Y. A., Dolhain, R. J. E. M., van de Geijn, F. E., Willemsen, S. P., & Hazes, J. M. W. (2008) · Arthritis Care & Research · doi:10.1002/art.24003 · Cited by 527 · see citing works

HLA‐G and immune tolerance in pregnancy

Hunt, J. S., Petroff, M. G., McIntire, R. H., & Ober, C. (2005) · The FASEB Journal · doi:10.1096/fj.04-2078rev · Cited by 523 · see citing works

Arsenic Exposure Perturbs the Gut Microbiome and Its Metabolic Profile in Mice: An Integrated Metagenomics and Metabolomics Analysis

Lü, K., Abo, R., Schlieper, K. A., Graffam, M. E., Levine, S. S., Wishnok, J. S., Swenberg, J. A., Tannenbaum, S. R., & Fox, J. G. (2014) · Environmental Health Perspectives · doi:10.1289/ehp.1307429 · Cited by 516 · see citing works

Beyond stem cells: self-renewal of differentiated macrophages

Sieweke, M. H., & Allen, J. E. (2013) · Science · doi:10.1126/science.1242974 · Cited by 503 · see citing works

Transgenerational effects of prenatal exposure to the 1944–45 Dutch famine

Veenendaal, M., Painter, R., de Rooij, Sr., Bossuyt, P., van der Post, J., Gluckman, P., Hanson, M., & Roseboom, T. (2013) · BJOG: An International Journal of Obstetrics & Gynaecology · doi:10.1111/1471-0528.12136 · Cited by 477 · 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

Neonatal Innate TLR-Mediated Responses Are Distinct from Those of Adults

Kollmann, T. R., Crabtree, J., Rein‐Weston, A., Blimkie, D., Thommai, F., Wang, X. Y., Lavoie, P. M., Furlong, J., Fortuno, E. S., Hajjar, A. M., et al. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0901481 · Cited by 465 · see citing works

Selective, stable demethylation of the interleukin-2 gene enhances transcription by an active process

Bruniquel, D., & Schwartz, R. H. (2003) · Nature Immunology · doi:10.1038/ni887 · Cited by 457 · see citing works

Health effects of passive smoking

Chinn, S., Rona, R. J., Cook, D. G., Strachan, D. P., & Carey, I. M. (1999) · Thorax · doi:10.1136/thx.54.5.468a · Cited by 445 · see citing works

Partition of Environmental Chemicals between Maternal and Fetal Blood and Tissues

Needham, L. L., Grandjean, P., Heinzow, B., Jørgensen, P. J., Nielsen, F., Patterson, D. G., Sjödin, A., Turner, W. E., & Weihe, P. (2010) · Environmental Science & Technology · doi:10.1021/es1019614 · Cited by 406 · see citing works

Chronic helminth infections induce immunomodulation: Consequences and mechanisms

van Riet, E., Hartgers, F. C., & Yazdanbakhsh, M. (2007) · Immunobiology · doi:10.1016/j.imbio.2007.03.009 · Cited by 393 · see citing works

Immunologic Effects of Background Exposure to Polychlorinated Biphenyls and Dioxins in Dutch Preschool Children

Weisglas‐Kuperus, N., Patandin, S., Berbers, G. A. M., Sas, T., Mulder, P. G. H., Sauer, P. J. J., & Hooijkaas, H. (2000) · Environmental Health Perspectives · doi:10.1289/ehp.001081203 · Cited by 384 · see citing works

Health effects of passive smoking. 1. Parental smoking and lower respiratory illness in infancy and early childhood.

Strachan, D. P., & Cook, D. G. (1997) · Thorax · doi:10.1136/thx.52.10.905 · Cited by 383 · see citing works

Micronutrient malnutrition, infection, and immunity: An overview

Bhaskaram, P. (2002) · Nutrition Reviews · doi:10.1301/00296640260130722 · Cited by 361 · see citing works

Trained Immunity or Tolerance: Opposing Functional Programs Induced in Human Monocytes after Engagement of Various Pattern Recognition Receptors

Ifrim, D. C., Quintin, J., Joosten, L. A. B., Jacobs, C. W. M., Jansen, T., Jacobs, L., Gow, N. A. R., Williams, D. L., van der Meer, J. W. M., & Netea, M. G. (2014) · Clinical and Vaccine Immunology · doi:10.1128/cvi.00688-13 · Cited by 358 · see citing works

Intraembryonic, but Not Yolk Sac Hematopoietic Precursors, Isolated before Circulation, Provide Long-Term Multilineage Reconstitution

Cumano, A., Ferraz, J. C., Klaine, M., Santo, J. P. D., & Godin, I. (2001) · Immunity · doi:10.1016/s1074-7613(01)00190-x · Cited by 345 · see citing works

Effects of Arsenic on Maternal and Fetal Health

Vahter, M. (2009) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-080508-141102 · Cited by 341 · see citing works

Influence of early gut microbiota on the maturation of childhood mucosal and systemic immune responses: Gut microbiota and immune responses

Sjögren, Y. M., Tomicic, S., Lundberg, A., Böttcher, M. F., Björkstén, B., Sverremark‐Ekström, E., & Jenmalm, M. C. (2009) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2009.03326.x · Cited by 337 · see citing works

Zinc Deficiency, Infectious Disease and Mortality in the Developing World

Black, R. E. (2003) · Journal of Nutrition · doi:10.1093/jn/133.5.1485s · Cited by 332 · see citing works

Pre- and Postnatal Exposure to Perfluorinated Compounds (PFCs)

Fromme, H., Mosch, C., Morovitz, M., Alba‐Alejandre, I., Boehmer, S., Kiranoglu, M., Faber, F. L., Hannibal, I., Genzel‐Boroviczény, O., Koletzko, B. V., et al. (2010) · Environmental Science & Technology · doi:10.1021/es101184f · Cited by 332 · see citing works

Adverse health effects of prenatal and postnatal tobacco smoke exposure on children

Hofhuis, W. (2003) · Archives of Disease in Childhood · doi:10.1136/adc.88.12.1086 · Cited by 329 · see citing works

Pregnancy and Susceptibility to Infectious Diseases

Sappenfield, E. C., Jamieson, D. J., & Kourtis, A. P. (2013) · Infectious Diseases in Obstetrics and Gynecology · doi:10.1155/2013/752852 · Cited by 323 · see citing works

Impairment of Tetanus Toxoid-Specific Thl-like Immune Responses in Humans Infected with Schistosoma mansoni

Sabin, E., Araújo, M. I., Carvalho, E. M., & Pearce, E. J. (1996) · The Journal of Infectious Diseases · doi:10.1093/infdis/173.1.269 · Cited by 322 · see citing works

A Taxonomic Signature of Obesity in the Microbiome? Getting to the Guts of the Matter

Finucane, M. M., Sharpton, T. J., Laurent, T. J., & Pollard, K. S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0084689 · Cited by 321 · see citing works

Bacteria and inflammatory cells in fetal membranes do not always cause preterm labor

Steel, J. H., Malatos, S., Kennea, N., Edwards, A. D., Miles, L., Duggan, P., Reynolds, P. R., Feldman, R. G., & Sullivan, M. H. F. (2005) · Pediatric Research · doi:10.1203/01.pdr.0000153869.96337.90 · Cited by 317 · see citing works

Urinary Cadmium, Impaired Fasting Glucose, and Diabetes in the NHANES III

Schwartz, G. G., Il’yasova, D., & Ivanova, A. (2003) · Diabetes Care · doi:10.2337/diacare.26.2.468 · Cited by 295 · see citing works

The role of the placenta in fetal exposure to heavy metals

Gundacker, C., & Hengstschläger, M. (2012) · Wiener Medizinische Wochenschrift · doi:10.1007/s10354-012-0074-3 · Cited by 285 · see citing works

Preventing Tuberculosis with Bacillus Calmette-Guérin Vaccine: A Meta-Analysis of the Literature

Brewer, T. F. (2000) · Clinical Infectious Diseases · doi:10.1086/314072 · Cited by 283 · see citing works

Early-life environmental determinants of allergic diseases and the wider pandemic of inflammatory noncommunicable diseases

Prescott, S. L. (2012) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2012.11.019 · Cited by 277 · see citing works

Arsenic immunotoxicity: a review

Dangleben, N. L., Skibola, C. F., & Smith, M. T. (2013) · Environmental Health · doi:10.1186/1476-069x-12-73 · Cited by 275 · 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

<i>Plasmodium falciparum</i>Isolates from Infected Pregnant Women and Children Are Associated with Distinct Adhesive and Antigenic Properties

Beeson, J. G., Brown, G. V., Molyneux, M. E., Mhango, C., Dzinjalamala, F., & Rogerson, S. J. (1999) · The Journal of Infectious Diseases · doi:10.1086/314899 · Cited by 266 · see citing works

Pathogens and the placental fortress

Robbins, J. R., & Bakardjiev, A. I. (2011) · Current Opinion in Microbiology · doi:10.1016/j.mib.2011.11.006 · Cited by 264 · 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

Prenatal Exposures to Persistent and Non‐Persistent Organic Compounds and Effects on Immune System Development

Hertz‐Picciotto, I., Park, H., Dostal, M., Kocan, A., Trnovec, T., & Sram, R. (2008) · Basic &amp; Clinical Pharmacology &amp; Toxicology · doi:10.1111/j.1742-7843.2007.00190.x · Cited by 253 · see citing works

Competing Interactions between Micro-RNAs Determine Neural Progenitor Survival and Proliferation after Ethanol Exposure: Evidence from an <i>Ex Vivo</i> Model of the Fetal Cerebral Cortical Neuroepithelium

Sathyan, P., Golden, H. B., & Miranda, R. C. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1269-07.2007 · Cited by 245 · see citing works

The Human Embryo, but Not Its Yolk Sac, Generates Lympho-Myeloid Stem Cells

Tavian, M., Robin, C., Coulombel, L., & Péault, B. (2001) · Immunity · doi:10.1016/s1074-7613(01)00193-5 · Cited by 231 · see citing works

Human Infection with Ascaris lumbricoides Is Associated with Suppression of the Interleukin-2 Response to Recombinant Cholera Toxin B Subunit following Vaccination with the Live Oral Cholera Vaccine CVD 103-HgR

Cooper, P. J., Chico, M. E., Sandoval, C. A., Espinel, I., Guevara, A., Levine, M. M., Griffin, G. E., & Nutman, T. B. (2001) · Infection and Immunity · doi:10.1128/iai.69.3.1574-1580.2001 · Cited by 231 · see citing works

Small Randomized Trial Among Low–birth-weight Children Receiving Bacillus Calmette-Guérin Vaccination at First Health Center Contact

Biering-Sørensen, S. R., Aaby, P., Napirna, B. M., Roth, A., Ravn, H., Rodrigues, A., Whittle, H. C., & Benn, C. S. (2011) · The Pediatric Infectious Disease Journal · doi:10.1097/inf.0b013e3182458289 · Cited by 226 · see citing works

Reduced Antibody Responses to Vaccinations in Children Exposed to Polychlorinated Biphenyls

Heilmann, C. J., Grandjean, P., Weihe, P., Nielsen, F., & Budtz–Jørgensen, E. (2006) · PLoS Medicine · doi:10.1371/journal.pmed.0030311 · Cited by 224 · see citing works

Human milk metagenome: a functional capacity analysis

Ward, T., Hosid, S., Ioshikhes, I. P., & Altosaar, I. (2013) · BMC Microbiology · doi:10.1186/1471-2180-13-116 · Cited by 220 · see citing works

HIV-exposed uninfected children: a growing population with a vulnerable immune system?

Afran, L., Garcia-Knight, M., Nduati, E. W., Urban, B. C., Heyderman, R. S., & Rowland‐Jones, S. (2013) · Clinical & Experimental Immunology · doi:10.1111/cei.12251 · Cited by 219 · see citing works

Characterizing the Pregnancy Immune Phenotype: Results of the Viral Immunity and Pregnancy (VIP) Study

Kraus, T., Engel, S. M., SPERLING, R. S., Kellerman, L., Lo, Y., Wallenstein, S. R., Escribese, M. M., Garrido, J. L. V., Singh, T., Loubeau, M., et al. (2011) · Journal of Clinical Immunology · doi:10.1007/s10875-011-9627-2 · Cited by 216 · see citing works

Placental transfer and concentrations of cadmium, mercury, lead, and selenium in mothers, newborns, and young children

Chen, Z., Myers, R. A., Wei, T., Bind, E. P., Kassim, P. A., Wang, G., Ji, Y., Hong, X., Caruso, D., Bartell, T. R., et al. (2014) · Journal of Exposure Science & Environmental Epidemiology · doi:10.1038/jes.2014.26 · Cited by 215 · see citing works

Reciprocal seasonal variation in vitamin D status and tuberculosis notifications in Cape Town, South Africa

Martineau, A. R., Nhamoyebonde, S., Oni, T., Rangaka, M. X., Marais, S., Bangani, N., Tsekela, R., Bashe, L., Azevedo, V. D., Caldwell, J., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1111825108 · Cited by 208 · 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

Epigenetic Remodeling of the IL-2 and IFN -γ Loci in Memory CD8 T Cells Is Influenced by CD4 T Cells

Northrop, J. K., Thomas, R. M., Wells, A. D., & Shen, H. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.2.1062 · Cited by 203 · see citing works

Influence of BCG vaccine strain on the immune response and protection against tuberculosis

Ritz, N., Hanekom, W. A., Robins-Browne, R. M., Britton, W. J., & Curtis, N. C. (2008) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2008.00118.x · Cited by 201 · see citing works

Nutritionally Mediated Programming of the Developing Immune System

Palmer, A. C. (2011) · Advances in Nutrition · doi:10.3945/an.111.000570 · Cited by 198 · see citing works

Immunology of Parasitic Helminth Infections

MacDonald, A. S., Araújo, M. I., & Pearce, E. J. (2002) · Infection and Immunity · doi:10.1128/iai.70.2.427-433.2002 · Cited by 197 · see citing works

Maternal smoking is associated with impaired neonatal toll-like-receptor-mediated immune responses

Noakes, P. S., Hale, J., Thomas, R., Lane, C., Devadason, S. G., & Prescott, S. L. (2006) · European Respiratory Journal · doi:10.1183/09031936.06.00050206 · Cited by 191 · see citing works

In Utero Exposures, Infant Growth, and DNA Methylation of Repetitive Elements and Developmentally Related Genes in Human Placenta

Wilhelm-Benartzi, C. S., Houseman, E. A., Maccani, M. A., Poage, G. M., Koestler, D. C., Langevin, S. M., Gagne, L. A., Banister, C. E., Padbury, J. F., & Marsit, C. J. (2011) · Environmental Health Perspectives · doi:10.1289/ehp.1103927 · Cited by 190 · see citing works

Alcohol Abuse in Pregnant Women: Effects on the Fetus and Newborn, Mode of Action and Maternal Treatment

Ornoy, A., & Ergaz, Z. (2010) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph7020364 · Cited by 188 · see citing works

Role of Innate Host Defenses in Susceptibility to Early-Onset Neonatal Sepsis

Wynn, J. L., & Levy, O. (2010) · Clinics in Perinatology · doi:10.1016/j.clp.2010.04.001 · Cited by 182 · see citing works

Differential DNA Methylation in Umbilical Cord Blood of Infants Exposed to Low Levels of Arsenic in Utero

Koestler, D. C., Avissar-Whiting, M., Houseman, E. A., Karagas, M. R., & Marsit, C. J. (2013) · Environmental Health Perspectives · doi:10.1289/ehp.1205925 · Cited by 180 · see citing works

Foxp3+ Regulatory T Cell Expansion Required for Sustaining Pregnancy Compromises Host Defense against Prenatal Bacterial Pathogens

Rowe, J. H., Ertelt, J. M., Aguilera, M., Farrar, M. A., & Way, S. S. (2011) · Cell Host & Microbe · doi:10.1016/j.chom.2011.06.005 · Cited by 179 · see citing works

Immune Deficiency in Fetal Alcohol Syndrome

Johnson, S., Knight, R., Marmer, D. J., & Steele, R. W. (1981) · Pediatric Research · doi:10.1203/00006450-198106000-00005 · Cited by 177 · see citing works

Uninfected but not unaffected: chronic maternal infections during pregnancy, fetal immunity, and susceptibility to postnatal infections

Dauby, N., Goetghebuer, T., Kollmann, T. R., Lévy, J., & Marchant, A. (2012) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(11)70341-3 · Cited by 177 · 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

Maternal and cord blood miR-223 expression associates with prenatal tobacco smoke exposure and low regulatory T-cell numbers

Herberth, G., Bauer, M., Gasch, M., Hinz, D., Röder, S. W., Olek, S., Kohajda, T., Rolle-Kampczyk, U. E., von Bergen�, M., Sack, U., et al. (2013) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2013.06.036 · Cited by 172 · see citing works

Ontogeny of Toll-Like Receptor Mediated Cytokine Responses of Human Blood Mononuclear Cells

Corbett, N., Blimkie, D., Ho, K., Cai, B., Sutherland, D. P., Kallos, A., Crabtree, J., Rein‐Weston, A., Lavoie, P. M., Turvey, S. E., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015041 · Cited by 170 · see citing works

Developmental exposure to TCDD reduces fertility and negatively affects pregnancy outcomes across multiple generations

Bruner‐Tran, K. L., & Osteen, K. G. (2010) · Reproductive Toxicology · doi:10.1016/j.reprotox.2010.10.003 · Cited by 164 · see citing works

The influence of the mode of delivery on circulating cytokine concentrations in the perinatal period

Malamitsi‐Puchner, A., Protonotariou, E., Boutsikou, Τ., Makrakis, E., Sarandakou, A., & Creatsas, G. K. (2005) · Early Human Development · doi:10.1016/j.earlhumdev.2004.10.017 · Cited by 162 · see citing works

Prenatal Arsenic Exposure and DNA Methylation in Maternal and Umbilical Cord Blood Leukocytes

Kile, M. L., Baccarelli, A., Hoffman, E. B., Tarantini, L., Quamruzzaman, Q., Rahman, M., Mahiuddin, G., Mostofa, G., Hsueh, Y., Wright, R. O., et al. (2012) · Environmental Health Perspectives · doi:10.1289/ehp.1104173 · Cited by 155 · see citing works

In vitro evaluation of the immunotoxic potential of perfluorinated compounds (PFCs)

Corsini, E., Avogadro, A., Galbiati, V., Dell’Agli, M., Marinovich, M., Galli, C. L., & Germolec, D. R. (2010) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2010.11.004 · Cited by 153 · see citing works

Developmental Exposure to Lead Causes Persistent Immunotoxicity in Fischer 344 Rats

Miller, T. E., Golemboski, K. A., Ha, R. S., Bunn, T. L., Sanders, F. S., & Dietert, R. R. (1998) · Toxicological Sciences · doi:10.1093/toxsci/42.2.129 · Cited by 152 · see citing works

HIV-Exposed Uninfected Infants are at Increased Risk for Severe Infections in the First Year of Life

Slogrove, A. L., Reikie, B. A., Naidoo, S., de Beer, C., Ho, K., Cotton, M. F., Bettinger, J. A., Speert, D. P., Esser, M., & Kollmann, T. R. (2012) · Journal of Tropical Pediatrics · doi:10.1093/tropej/fms019 · Cited by 146 · see citing works

Do Antenatal Parasite Infections Devalue Childhood Vaccination?

LaBeaud, A. D., Malhotra, I. J., King, M. J., King, C. L., & King, C. H. (2009) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0000442 · Cited by 133 · see citing works

Month of birth, vitamin D and risk of immune-mediated disease: a case control study

Disanto, G., Chaplin, G., Morahan, J. M., Giovannoni, G., Hyppönen, E., Ebers, G. C., & Ramagopalan, S. V. (2012) · BMC Medicine · doi:10.1186/1741-7015-10-69 · Cited by 133 · see citing works

Distinct methylation patterns in histone H3 at Lys-4 and Lys-9 correlate with up- & down-regulation of genes by ethanol in hepatocytes.

Pal-Bhadra, M., Bhadra, U., Jackson, D. E., Mamatha, L., Park, P.-H., & Shukla, S. D. (2007) · Life Science · doi:10.1016/j.lfs.2007.07.030 · Cited by 130 · see citing works

Neonatal Thyroid Function in Seveso 25 Years after Maternal Exposure to Dioxin

Baccarelli, A., Giacomini, S., Corbetta, C., Landi, M. T., Bonzini, M., Consonni, D., Grillo, P., Patterson, D. G., Pesatori, A. C., & Bertazzi, P. A. (2008) · PLoS Medicine · doi:10.1371/journal.pmed.0050161 · Cited by 128 · see citing works

Effects of arsenic exposure on DNA methylation in cord blood samples from newborn babies and in a human lymphoblast cell line

Intarasunanont, P., Navasumrit, P., Waraprasit, S., Chaisatra, K., Suk, W. A., Mahidol, C., & Ruchirawat, M. (2012) · Environmental Health · doi:10.1186/1476-069x-11-31 · Cited by 128 · see citing works

Patterns and Implications of Naturally Acquired Immune Responses to Environmental and Tuberculous Mycobacterial Antigens in Northern Malawi

Black, G. F., Dockrell, H. M., Crampin, A. C., Floyd, S., Weir, R. E., Bliss, L., Sichali, L., Mwaungulu, L., Kanyongoloka, H., Ngwira, B. M., et al. (2001) · The Journal of Infectious Diseases · doi:10.1086/322042 · Cited by 126 · see citing works

T-lymphocyte subsets in West African children: Impact of age, sex, and season

Lisse, I. M., Aaby, P., Whittle, H. C., Jensen, H., Engelmann, M. D. M., & Christensen, L. B. (1997) · The Journal of Pediatrics · doi:10.1016/s0022-3476(97)70313-5 · Cited by 125 · see citing works

The effects of maternal helminth and malaria infections on mother-to-child HIV transmission

Gallagher, M., Malhotra, I. J., Mungai, P., Wamachi, A. N., Kioko, J. M., Ouma, J. H., Muchiri, E. M., & King, C. L. (2005) · AIDS · doi:10.1097/01.aids.0000189846.90946.5d · Cited by 123 · see citing works

Interaction of pregnancy and autoimmune rheumatic disease

Østensen, M., Villiger, P. M., & Förger, F. (2011) · Autoimmunity Reviews · doi:10.1016/j.autrev.2011.11.013 · Cited by 122 · see citing works

In Utero Arsenic Exposure Is Associated With Impaired Thymic Function in Newborns Possibly Via Oxidative Stress and Apoptosis

Ahmed, S., Ahsan, K., Kippler, M. J., Mily, A., Wagatsuma, Y., Hoque, A. M. W., N’Gom, P. T., Arifeen, S. E., Raqib, R., & Vahter, M. (2012) · Toxicological Sciences · doi:10.1093/toxsci/kfs202 · Cited by 119 · see citing works

Non-specific effect of Bacille Calmette-Guérin vaccine on the immune response to routine immunisations

Ritz, N., Mui, M., Balloch, A., & Curtis, N. C. (2013) · Vaccine · doi:10.1016/j.vaccine.2013.03.059 · Cited by 118 · see citing works

Age-Dependent Maturation of Toll-Like Receptor-Mediated Cytokine Responses in Gambian Infants

Burl, S., Townend, J., Njie-Jobe, J., Cox, M., Adetifa, U. J., Touray, E. S., Philbin, V. J., Mancuso, C. J., Kampmann, B., Whittle, H. C., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0018185 · Cited by 118 · see citing works

HLA-G and HLA-E: fundamental and pathophysiological aspects

Carosella, E. D., Paul, P., Moreau, P., & Rouas‐Freiss, N. (2000) · Immunology Today · doi:10.1016/s0167-5699(00)01707-2 · Cited by 117 · see citing works

BCG Vaccination Induces Different Cytokine Profiles Following Infant BCG Vaccination in the UK and Malawi

Lalor, M. K., Floyd, S., Gorak‐Stolinska, P., Ben‐Smith, A., Weir, R. E., Smith, S. G., Newport, M. J., Blitz, R., Mvula, H., Branson, K. R., et al. (2011) · The Journal of Infectious Diseases · doi:10.1093/infdis/jir515 · Cited by 111 · see citing works

PCB exposure in utero and via breast milk. A review

Dekoning, E. P., & Karmaus, W. J. J. (2000) · Journal of Exposure Science & Environmental Epidemiology · doi:10.1038/sj.jea.7500090 · Cited by 110 · see citing works

Growth faltering due to breastfeeding cessation in uninfected children born to HIV-infected mothers in Zambia

Arpadi, S. M., Fawzy, A., Aldrovandi, G. M., Kankasa, C., Sinkala, M., Mwiya, M., Thea, D. M., & Kuhn, L. (2009) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.2009.27745 · Cited by 109 · see citing works

Cytokines and other immunological biomarkers in children's environmental health studies

Duramad, P., Tager, I. B., & Holland, N. (2007) · Toxicology Letters · doi:10.1016/j.toxlet.2007.05.017 · Cited by 105 · see citing works

Immune cell counts and risks of respiratory infections among infants exposed pre- and postnatally to organochlorine compounds: a prospective study

Glynn, A. W., Thuvander, A., Aune, M., Johannisson, A., Darnerud, P. O., Ronquist, G., & Cnattingius, S. (2008) · Environmental Health · doi:10.1186/1476-069x-7-62 · Cited by 103 · see citing works

Maternal filarial infection as risk factor for infection in children

Lammie, P. J., Hitch, W. L., Walker, E. M., Hightower, A. W., & Eberhard, M. L. (1991) · The Lancet · doi:10.1016/0140-6736(91)92661-k · Cited by 102 · see citing works

Infection with parasitic nematodes confounds vaccination efficacy

Urban, J. F., Steenhard, N. R., Solano-Aguilar, G. I., Dawson, H. D., Iweala, O. I., Nagler‐Anderson, C., Noland, G. S., Kumar, N., Anthony, R. M., Shea‐Donohue, T., et al. (2007) · Veterinary Parasitology · doi:10.1016/j.vetpar.2007.05.006 · Cited by 97 · see citing works

Nutrition and the Immune System

Kubena, K. S., & McMurray, D. N. (1996) · Journal of the American Dietetic Association · doi:10.1016/s0002-8223(96)00297-0 · Cited by 94 · see citing works

Developmental Immunotoxicology: Focus on Health Risks

Dietert, R. R. (2008) · Chemical Research in Toxicology · doi:10.1021/tx800198m · Cited by 93 · see citing works

Early life response to infection

Ghazal, P., Dickinson, P., & Smith, C. (2013) · Current Opinion in Infectious Diseases · doi:10.1097/qco.0b013e32835fb8bf · Cited by 92 · see citing works

Immune modulation by helminthic infections: worms and viral infections

Kamal, S. M., & Khalifa, K. (2006) · Parasite Immunology · doi:10.1111/j.1365-3024.2006.00909.x · Cited by 91 · see citing works

In-utero exposure to maternal HIV infection alters T-cell immune responses to vaccination in HIV-uninfected infants

Kidzeru, E. B., Hesseling, A. C., Passmore, J.-A. S., Myer, L., Gamieldien, H., Tchakoute, C. T., Gray, C. M., Sodora, D. L., & Jaspan, H. B. (2014) · AIDS · doi:10.1097/qad.0000000000000292 · Cited by 91 · see citing works

Prenatal and childhood Mediterranean diet and the development of asthma and allergies in children

Chatzi, L., & Kogevinas, M. (2009) · Public Health Nutrition · doi:10.1017/s1368980009990474 · Cited by 91 · see citing works

Prenatal immunotoxicant exposure and postnatal autoimmune disease.

Holladay, S. D. (1999) · Environmental Health Perspectives · doi:10.1289/ehp.99107s5687 · Cited by 89 · see citing works

Maternal Alcohol Abuse and Neonatal Infection

Gauthier, T. W., Drews‐Botsch, C., Falek, A., Coles, C. D., & Brown, L. A. S. (2005) · Alcoholism Clinical and Experimental Research · doi:10.1097/01.alc.0000167956.28160.5e · Cited by 88 · see citing works

Human Immunodeficiency Virus (HIV)–Specific Cellular Immune Responses in Newborns Exposed to HIV In Utero

Kuhn, L., Meddows‐Taylor, S., Gray, G., & Tiemessen, C. T. (2002) · Clinical Infectious Diseases · doi:10.1086/338153 · Cited by 86 · see citing works

Survival of Infants Born to HIV-Positive Mothers, by Feeding Modality, in Rakai, Uganda

Kagaayi, J., Gray, R. H., Brahmbhatt, H., Kigozi, G., Nalugoda, F. K., Wabwire‐Mangen, F., Serwadda, D., Sewankambo, N. K., Ddungu, V., Ssebagala, D., et al. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003877 · Cited by 84 · see citing works

CORD BLOOD LYMPHOCYTE FUNCTIONS IN NEWBORNS FROM A REMOTE MARITIME POPULATION EXPOSED TO ORGANOCHLORINES AND METHYLMERCURY

Belles‐Isles, M., Ayotte, P., Dewailly, É., Weber, J., & Roy, R. (2002) · Journal of Toxicology and Environmental Health · doi:10.1080/152873902753396794 · Cited by 84 · see citing works

Nonspecific Effects of Vaccines and the Reduction of Mortality in Children

Shann, F. A. (2013) · Clinical Therapeutics · doi:10.1016/j.clinthera.2013.01.007 · Cited by 83 · see citing works

Altered Innate Immune Development in HIV-Exposed Uninfected Infants

Reikie, B. A., Adams, R. C. M., Leligdowicz, A., Ho, K., Naidoo, S., Ruck, C. E., de Beer, C., Preiser, W., Cotton, M. F., Speert, D. P., et al. (2014) · JAIDS Journal of Acquired Immune Deficiency Syndromes · doi:10.1097/qai.0000000000000161 · Cited by 80 · see citing works

Antibody Responses to Vaccination among South African HIV-Exposed and Unexposed Uninfected Infants during the First 2 Years of Life

Reikie, B. A., Naidoo, S., Ruck, C. E., Slogrove, A. L., de Beer, C., la Grange, H., Adams, R. C. M., Ho, K., Smolen, K. K., Speert, D. P., et al. (2012) · Clinical and Vaccine Immunology · doi:10.1128/cvi.00557-12 · Cited by 72 · see citing works

Impaired Humoral Response to Vaccines among HIV-Exposed Uninfected Infants

Abramczuk, B. M., Mazzola, T. N., Moreno, Y. M. F., Zorzeto, T. Q., Quintilio, W., Wolf, P. S., Blotta, M. H. S. L., Morcillo, A. M., da Silva, M. T. N., & Vilela, M. M. D. S. (2011) · Clinical and Vaccine Immunology · doi:10.1128/cvi.05065-11 · Cited by 71 · see citing works

Influence of Maternal Filariasis on Childhood Infection and Immunity toWuchereria bancroftiin Kenya

Malhotra, I. J., Ouma, J. H., Wamachi, A. N., Kioko, J., Mungai, P., Njzovu, M., Kazura, J. W., & King, C. L. (2003) · Infection and Immunity · doi:10.1128/iai.71.9.5231-5237.2003 · Cited by 71 · see citing works

Prenatal T Cell Immunity toWuchereria bancroftiand Its Effect on Filarial Immunity and Infection Susceptibility during Childhood

Malhotra, I. J., Mungai, P., Wamachi, A. N., Tisch, D. J., Kioko, J. M., Ouma, J. H., Muchiri, E. M., Kazura, J. W., & King, C. L. (2006) · The Journal of Infectious Diseases · doi:10.1086/500472 · Cited by 70 · see citing works

Commensal Bacteria and Expression of Two Major Intestinal Chemokines, TECK/CCL25 and MEC/CCL28, and Their Receptors

Meurens, F., Berri, M., Siggers, R. H., Willing, B. P., Salmon, H., Kessel, A. G. V., & Gerdts, V. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000677 · Cited by 70 · see citing works

Nutrition in early life, immune-programming and allergies: the role of epigenetics.

Amarasekera, M., Prescott, S. L., & Palmer, D. J. (2013) · PubMed · Cited by 68 · see citing works

HIV, infant feeding and more perils for poor people: new WHO guidelines encourage review of formula milk policies

Coutsoudis, A. (2008) · Bulletin of the World Health Organization · doi:10.2471/blt.07.041673 · Cited by 66 · see citing works

What, if any, is the effect of malnutrition on immunological competence?

Morgan, G. J. (1997) · The Lancet · doi:10.1016/s0140-6736(96)12038-9 · Cited by 65 · see citing works

Influence of Socioeconomic Status Trajectories on Innate Immune Responsiveness in Children

Azad, M. B., Lissitsyn, Y., Miller, G. E., Becker, A. B., HayGlass, K. T., & Kozyrskyj, A. L. (2012) · PLoS ONE · doi:10.1371/journal.pone.0038669 · Cited by 64 · see citing works

Current Status of Developmental Immunotoxicity

DeWitt, J. C., Peden‐Adams, M. M., Keil, D. E., & Dietert, R. R. (2011) · Toxicologic Pathology · doi:10.1177/0192623311427709 · Cited by 64 · see citing works

Role of diet in the development of immune tolerance in the context of allergic disease

West, C. E., Videky, D. J., & Prescott, S. L. (2010) · Current Opinion in Pediatrics · doi:10.1097/mop.0b013e32833d96ef · Cited by 61 · see citing works

Innate immune memory: implications for development of pediatric immunomodulatory agents and adjuvanted vaccines

Levy, O., & Netea, M. G. (2013) · Pediatric Research · doi:10.1038/pr.2013.214 · Cited by 61 · see citing works

Induction of Antigen-Specific Immunity in Human Neonates and Infants

Wilson, C. B., & Kollmann, T. R. (2008) · KARGER eBooks · doi:10.1159/000113493 · Cited by 60 · see citing works

Pattern recognition receptor-mediated cytokine response in infants across 4 continents⋆

Smolen, K. K., Ruck, C. E., Fortuno, E. S., Ho, K., Dimitriu, P. A., Mohn, W. W., Speert, D. P., Cooper, P. J., Esser, M., Goetghebuer, T., et al. (2013) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2013.09.038 · Cited by 57 · see citing works

Unique Gene Expression Profiles in Infants Vaccinated with Different Strains ofMycobacterium bovisBacille Calmette-Guerin

Wu, B., Huang, C., García‐García, L., Ponce‐de‐León, A., Sifuentes‐Osornio, J., Bobadilla-del-Valle, M., Ferreira, L., Canizales‐Quintero, S., Small, P. M., Kato‐Maeda, M., et al. (2007) · Infection and Immunity · doi:10.1128/iai.00244-07 · Cited by 56 · see citing works

Half-life of each dioxin and PCB congener in the human body

Ogura, I. (2004) · Cited by 53 · see citing works

Blood-Forming Endothelium in Human Ontogeny: Lessons From In Utero Development and Embryonic Stem Cell Culture

Zambidis, E. T., Oberlin, E., Tavian, M., & Péault, B. (2006) · Trends in Cardiovascular Medicine · doi:10.1016/j.tcm.2006.01.005 · Cited by 52 · see citing works

1999 Pediatric Academic Societies' Annual Meeting

(1999) · Archives of Pediatrics and Adolescent Medicine · doi:10.1001/archpedi.153.4.418 · Cited by 52 · see citing works

Effect of Cadmium Body Burden on Immune Response of School Children

Ritz, B. R., Heinrich, J., Wjst, M., Wichmann, E., & Krause, C. (1998) · Archives of Environmental Health An International Journal · doi:10.1080/00039899809605708 · Cited by 51 · see citing works

Evidence for In Utero Sensitization toAscaris lumbricoidesin Newborns of Mothers with Ascariasis

Guadalupe, I., Mitre, E. E. S., Benitez, S. M., Chico, M. E., Nutman, T. B., & Cooper, P. J. (2009) · The Journal of Infectious Diseases · doi:10.1086/599214 · Cited by 51 · see citing works

Effects of Cessation of Breastfeeding in HIV-1-Exposed, Uninfected Children in Malawi

Taha, T. E., Hoover, D. R., Chen, S., Kumwenda, J., Mipando, L., Nkanaunena, K., Thigpen, M. C., Taylor, A. W., Fowler, M. G., & MOFENSON, L. M. (2011) · Clinical Infectious Diseases · doi:10.1093/cid/cir413 · Cited by 51 · see citing works

Molecular interactions in the placenta during malaria infection

Mens, P. F., Bojtor, E. C., & Schallig, H. D. F. H. (2010) · European Journal of Obstetrics & Gynecology and Reproductive Biology · doi:10.1016/j.ejogrb.2010.05.013 · Cited by 48 · see citing works

Immune function in rural Gambian children is not related to season of birth, birth size, or maternal supplementation status

Moore, S. E., Collinson, A. C., & Prentice, A. M. (2001) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/74.6.840 · Cited by 48 · see citing works

Impact of maternal HIV-1 viremia on lymphocyte subsets among HIV-exposed uninfected infants: protective mechanism or immunodeficiency

Kakkar, F., Lamarre, V., Ducruet, T., Boucher, M., Valois, S., Soudeyns, H., & Lapointe, N. (2014) · BMC Infectious Diseases · doi:10.1186/1471-2334-14-236 · Cited by 47 · see citing works

The Plausibility of Micronutrient Deficiency in Relationship to Perinatal Infection

Goldenberg, R. L. (2003) · Journal of Nutrition · doi:10.1093/jn/133.5.1645s · Cited by 47 · see citing works

Decrease in the Effectiveness of Bacille Calmette‐Guérin Vaccine against Pulmonary Tuberculosis: A Consequence of Increased Immune Suppression by Microbial Antioxidants, Not Overattenuation

Kernodle, D. S. (2010) · Clinical Infectious Diseases · doi:10.1086/653533 · Cited by 44 · see citing works

Ontogeny of Toll-Like and NOD-Like Receptor-Mediated Innate Immune Responses in Papua New Guinean Infants

Lisciandro, J. G., Prescott, S. L., Nadal‐Sims, M. G., Devitt, C. J., Pomat, W. S., Siba, P. M., Tulić, M. K., Holt, P. G., Strickland, D. H., & van den Biggelaar, A. H. J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036793 · Cited by 41 · see citing works

Maternal Geohelminth Infections Are Associated with an Increased Susceptibility to Geohelminth Infection in Children: A Case-Control Study

Mehta, R. S., Rodríguez, A., Chico, M. E., Guadalupe, I., Broncano, N., Sandoval, C. A., Tupiza, F., Mitre, E. E. S., & Cooper, P. J. (2012) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0001753 · Cited by 40 · see citing works

Colostrum-derived B and T cells as an extra-lymphoid compartment of effector cell populations in humans

Peroni, D. G., Chirumbolo, S., Veneri, D., PIACENTINI, G. L., Tenero, L., Vella, A., Ortolani, R., Raffaelli, R., & Boner, A. L. (2012) · The Journal of Maternal-Fetal & Neonatal Medicine · doi:10.3109/14767058.2012.733744 · Cited by 39 · see citing works

Birth season and environmental influences on blood leucocyte and lymphocyte subpopulations in rural Gambian infants

Collinson, A. C., N’Gom, P. T., Moore, S. E., Morgan, G., & Prentice, A. M. (2008) · BMC Immunology · doi:10.1186/1471-2172-9-18 · Cited by 38 · see citing works

The Effect of Maternal Helminth Infection on Maternal and Neonatal Immune Function and Immunity to Tuberculosis

Hagos, D. G., Desta, K., Desalegn, G., Howe, R., & Abebe, M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0093429 · Cited by 29 · see citing works

Immune response to Bordetella pertussis is associated with season and undernutrition in Senegalese children

Gaayeb, L., Pinçon, C., Cames, C., Sarr, J.-B., Seck, M., Schacht, A., Remoué, F., Hermann, E., & Riveau, G. J. (2014) · Vaccine · doi:10.1016/j.vaccine.2014.03.086 · Cited by 28 · see citing works

Maternal Selenium Nutrition and Neonatal Immune System Development

Dylewski, M. L., Mastro, A. M., & Picciano, M. F. (2002) · Neonatology · doi:10.1159/000063088 · Cited by 27 · see citing works

The Immune System and Exposure to Xenobiotics in Animals

Cabassi, E. (2007) · Veterinary Research Communications · doi:10.1007/s11259-007-0074-8 · Cited by 26 · see citing works

HLA class I expression in the human placenta

Juch, H., Blaschitz, A., Dohr, G., & Hutter, H. (2012) · Wiener Medizinische Wochenschrift · doi:10.1007/s10354-012-0070-7 · Cited by 25 · see citing works

Prenatal Immunotoxicant Exposure and Postnatal Autoimmune Disease

Holladay, S. D. (1999) · Environmental Health Perspectives · doi:10.2307/3434328 · Cited by 21 · see citing works

The Window of Opportunity: Pre-Pregnancy to 24 Months of Age

(2008) · Nestlé Nutrition Institute Workshop series · doi:10.1159/isbn.978-3-8055-8388-6 · Cited by 17 · see citing works

HIV, infant feeding and more perils for poor people: new WHO guidelines encourage review of formula milk policies

Coutsoudis, A. (2008) · Bulletin of the World Health Organization · doi:10.2471/blt.07.041679 · Cited by 15 · see citing works

Long-term effects of perinatal nutrition on T lymphocyte kinetics in young Gambian men

Ghattas, H., Wallace, D. L., Solon, J. A., Henson, S. M., Zhang, Y., N’Gom, P. T., Aspinall, R., Morgan, G., Griffin, G. E., Prentice, A. M., et al. (2007) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/85.2.480 · Cited by 11 · see citing works

Mode of Delivery and Inflammatory Disorders

Ghia, J., & Khafipour, E. (2013) · Cited by 6 · see citing works

Chronic maternal infections during pregnancy

Strunk, T., Currie, A. J., Simmer, K. N., & Burgner, D. P. (2012) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(12)70228-1 · Cited by 3 · see citing works

Research Highlights

(2006) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1922 · Cited by 2 · see citing works

The Bidirectional Relationship of Depression and Inflammation: Double Trouble

Beurel, E., Toups, M., & Nemeroff, C. B. (2020) · Neuron · doi:10.1016/j.neuron.2020.06.002 · Cited by 2,136 · see citing works

Immune function and micronutrient requirements change over the life course

Maggini, S., Pierre, A., & Calder, P. C. (2018) · Nutrients · doi:10.3390/nu10101531 · Cited by 710 · see citing works

Protecting the Newborn and Young Infant from Infectious Diseases: Lessons from Immune Ontogeny

Kollmann, T. R., Kampmann, B., Mazmanian, S. K., Marchant, A., & Levy, O. (2017) · Immunity · doi:10.1016/j.immuni.2017.03.009 · Cited by 478 · see citing works

Urbanization and the gut microbiota in health and inflammatory bowel disease

Zuo, T., Kamm, M. A., Colombel, J., & Ng, S. C. (2018) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-018-0003-z · Cited by 294 · see citing works

Intestinal commensal bacteria mediate lung mucosal immunity and promote resistance of newborn mice to infection

Gray, J. K., Oehrle, K., Worthen, G. S., Alenghat, T., Whitsett, J. A., & Deshmukh, H. S. (2017) · Science Translational Medicine · doi:10.1126/scitranslmed.aaf9412 · Cited by 213 · see citing works

Serum Vaccine Antibody Concentrations in Adolescents Exposed to Perfluorinated Compounds

Grandjean, P., Heilmann, C. J., Weihe, P., Nielsen, F., Mogensen, U. B., & Budtz–Jørgensen, E. (2016) · Environmental Health Perspectives · doi:10.1289/ehp275 · Cited by 208 · 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

Postnatal Innate Immune Development: From Birth to Adulthood

Georgountzou, A., & Papadopoulos, N. G. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00957 · Cited by 204 · see citing works

Effects of psychotropic drugs on inflammation:Consequence or mediator of therapeutic effects in psychiatric treatment?

Baumeister, D., Ciufolini, S., & Mondelli, V. (2016) · Psychopharmacology · doi:10.1007/s00213-015-4044-5 · Cited by 183 · see citing works

The effects of early life adversity on the immune system

Elwenspoek, M. M. C., Kuehn, A., Muller, C. P., & Turner, J. D. (2017) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2017.05.012 · Cited by 180 · see citing works

Human Breast Milk: From Food to Active Immune Response With Disease Protection in Infants and Mothers

Lokossou, A. G., Kouakanou, L., Schumacher, A., & Zenclussen, A. C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.849012 · Cited by 201 · 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

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

Trained immunity of alveolar macrophages requires metabolic rewiring and type 1 interferon signaling

Zahalka, S., Starkl, P. M., Watzenboeck, M. L., Farhat, A., Radhouani, M., Deckert, F., Hladik, A., Lakovits, K., Oberndorfer, F., Lassnig, C., et al. (2022) · Mucosal Immunology · doi:10.1038/s41385-022-00528-5 · Cited by 125 · see citing works

Changes in Human Milk Immunoglobulin Profile During Prolonged Lactation

Czosnykowska-Łukacka, M., Lis-Kuberka, J., Królak‐Olejnik, B., & Orczyk‐Pawiłowicz, M. (2020) · Frontiers in Pediatrics · doi:10.3389/fped.2020.00428 · Cited by 117 · see citing works

Perfluorinated alkyl substances impede growth, reproduction, lipid metabolism and lifespan in Daphnia magna

Seyoum, A., Pradhan, A., Jass, J., & Olsson, P.-E. (2020) · Science of The Total Environment · doi:10.1016/j.scitotenv.2020.139682 · Cited by 108 · see citing works

Comparative transcriptional analysis of methylparaben and propylparaben in zebrafish

Bereketoğlu, C., & Pradhan, A. (2019) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2019.03.358 · Cited by 92 · see citing works

Vaccination as a preventative measure contributing to immune fitness

Laupèze, B., Giudice, G. D., Doherty, M. T., & der Most, R. G. V. (2021) · npj Vaccines · doi:10.1038/s41541-021-00354-z · Cited by 97 · see citing works

Next generation protein based Streptococcus pneumoniae vaccines

Pichichero, M. E., Khan, M. N., & Xu, Q. (2015) · Human Vaccines & Immunotherapeutics · doi:10.1080/21645515.2015.1052198 · Cited by 86 · see citing works

Blood transcriptomic comparison of individuals with and without autism spectrum disorder: A combined‐samples mega‐analysis

Tylee, D. S., Hess, J., Quinn, T. P., Barve, R., Huang, H., Zhang‐James, Y., Chang, J., Stamova, B. S., Sharp, F. R., Hertz‐Picciotto, I., et al. (2016) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.32511 · Cited by 74 · see citing works

Poverty and Targeted Immunotherapy: Survival in Children’s Oncology Group Clinical Trials for High-Risk Neuroblastoma

Bona, K. O., Li, Y., Winestone, L. E., Getz, K., Huang, Y.-S. V., Fisher, B. T., Desai, A. V., Richardson, T., Hall, M., Naranjo, A. H., et al. (2020) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djaa107 · Cited by 72 · see citing works

Comparison of Human Neonatal and Adult Blood Leukocyte Subset Composition Phenotypes

Prabhu, S. B., Rathore, D. K., Deepa, N., Chaudhary, A., Raza, S., Kanodia, P., Sopory, S., George, A., Rath, S., Bal, V., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0162242 · Cited by 69 · see citing works

Sepsis-Induced Immunosuppression in Neonates

Hibbert, J., Currie, A. J., & Strunk, T. (2018) · Frontiers in Pediatrics · doi:10.3389/fped.2018.00357 · Cited by 68 · see citing works

Genetic ancestry and population differences in levels of inflammatory cytokines in women: Role for evolutionary selection and environmental factors

Yao, S., Hong, C., Ruiz-Narváez, E., Evans, S. S., Zhu, Q., Schaefer, B. A., Yan, L., Coignet, M. V., Lunetta, K. L., Sucheston‐Campbell, L. E., et al. (2018) · PLoS Genetics · doi:10.1371/journal.pgen.1007368 · Cited by 66 · 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

Ecological Risks Due to Immunotoxicological Effects on Aquatic Organisms

Kataoka, C., & Kashiwada, S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22158305 · Cited by 69 · see citing works

Current scenario of COVID-19 in pediatric age group and physiology of immune and thymus response

Rehman, S., Majeed, T., Ansari, M. A., Ali, U., Sabit, H., & Al-Suhaimi, E. A. (2020) · Saudi Journal of Biological Sciences · doi:10.1016/j.sjbs.2020.05.024 · Cited by 58 · see citing works

The balance between protective and pathogenic immune responses to pneumonia in the neonatal lung is enforced by gut microbiota

Stevens, J., Steinmeyer, S. H., Bonfield, M., Peterson, L. S., Wang, T. C., Gray, J. K., Lewkowich, I. P., Xu, Y. J., Du, Y., Guo, M., et al. (2022) · Science Translational Medicine · doi:10.1126/scitranslmed.abl3981 · Cited by 50 · see citing works

Environmental risk factors associated with respiratory diseases in children with socioeconomic disadvantage

Cortés-Ramírez, J., Wilches-Vega, J. D., Pineda, O. M. P., Rod, J. E., Ayurzana, L., & Sly, P. D. (2021) · Heliyon · doi:10.1016/j.heliyon.2021.e06820 · Cited by 49 · see citing works

Health outcomes of young children born to mothers who received 2009 pandemic H1N1 influenza vaccination during pregnancy: retrospective cohort study

Walsh, L. K., Donelle, J., Dodds, L. A., Hawken, S., Wilson, K. R., Benchimol, E. I., Chakraborty, P. K., Guttmann, A., Kwong, J. C., MacDonald, N. E., et al. (2019) · BMJ · doi:10.1136/bmj.l4151 · Cited by 50 · see citing works

Trained Immunity for Personalized Cancer Immunotherapy: Current Knowledge and Future Opportunities

Lérias, J. R., de Sousa, E., Paraschoudi, G., Martins, J. D., Condeço, C., Figueiredo, N., Carvalho, C. T., Dodoo, E., Maia, A., Castillo-Martín, M., et al. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.02924 · Cited by 46 · see citing works

From Infections to Anthropogenic Inflicted Pathologies: Involvement of Immune Balance

Lee, F., & Lawrence, D. A. (2017) · Journal of Toxicology and Environmental Health Part B · doi:10.1080/10937404.2017.1412212 · Cited by 45 · see citing works

The Multifactorial Etiopathogeneses Interplay of Inflammatory Bowel Disease: An Overview

M’Koma, A. E. (2018) · Gastrointestinal Disorders · doi:10.3390/gidisord1010007 · Cited by 46 · see citing works

Mesoporous silica nanoparticle: Heralding a brighter future in cancer nanomedicine

Abbasi, M., Ghoran, S. H., Niakan, M. H., Jamali, K., Moeini, Z., Jangjou, A., Izadpanah, P., & Amani, A. M. (2021) · Microporous and Mesoporous Materials · doi:10.1016/j.micromeso.2021.110967 · Cited by 41 · see citing works

Disparate Tuberculosis Disease Development in Macaque Species Is Associated With Innate Immunity

Dijkman, K., Vervenne, R. A. W., Sombroek, C. C., Boot, C., Hofman, S., van Meijgaarden, K. E., Ottenhoff, T. H. M., Kocken, C. H. M., Haanstra, K. G., Vierboom, M., et al. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02479 · Cited by 40 · see citing works

Phage display of environmental protein toxins and virulence factors reveals the prevalence, persistence, and genetics of antibody responses

Angkeow, J. W., Monaco, D. R., Chen, A., Venkataraman, T., Jayaraman, S., Valencia, C., Sie, B. M., Liechti, T., Farhadi, P. N., Funez-dePagnier, G., et al. (2022) · Immunity · doi:10.1016/j.immuni.2022.05.002 · Cited by 40 · see citing works

Association of immune cell recruitment and BPD development

Heydarian, M., Schulz, C., Stoeger, T., & Hilgendorff, A. (2022) · Molecular and Cellular Pediatrics · doi:10.1186/s40348-022-00148-w · Cited by 40 · see citing works

Trained immunity: Perspectives for disease control strategy in marine mollusc aquaculture

Montagnani, C., Morga, B., Novoa, B., Gourbal, B., Saco, A., Rey-Campos, M., Bourhis, M., Riera, F., Vignal, E., Corporeau, C., et al. (2024) · Reviews in Aquaculture · doi:10.1111/raq.12906 · Cited by 38 · see citing works

Relationship between vaccination and nutritional status in children: Analysis of recent Demographic and Health Surveys

Solís-Soto, M. T., Paudel, D., & Nicoli, F. (2020) · Demographic Research · doi:10.4054/demres.2020.42.1 · Cited by 37 · see citing works

Development of allergic immunity in early life

Lloyd, C. M., & Saglani, S. (2017) · Immunological Reviews · doi:10.1111/imr.12562 · Cited by 34 · see citing works

Hsp70 overexpression in Drosophila hemocytes attenuates benzene‐induced immune and developmental toxicity via regulating ROS/JNK signaling pathway

D’Souza, L. C., Dwivedi, S., Raihan, F., Yathisha, U. G., Raghu, S. V., Mamatha, B. S., & Sharma, A. (2022) · Environmental Toxicology · doi:10.1002/tox.23520 · Cited by 32 · see citing works

Modeling the dynamics of neonatal CD8+ T‐cell responses

Reynaldi, A., Smith, N. L., Schlub, T. E., Venturi, V., Rudd, B. D., & Davenport, M. P. (2016) · Immunology and Cell Biology · doi:10.1038/icb.2016.47 · 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

Microbiome-induced antigen-presenting cell recruitment coordinates skin and lung allergic inflammation

Ubags, N. D. J., Trompette, A., Pernot, J., Nibbering, B., Wong, N. C., Pattaroni, C., Rapin, A., Nicod, L. P., Harris, N. L., & Marsland, B. J. (2020) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2020.06.030 · Cited by 30 · see citing works

Fusaric Acid immunotoxicity and MAPK activation in normal peripheral blood mononuclear cells and Thp-1 cells

Dhani, S., Nagiah, S., Naidoo, D. B., & Chuturgoon, A. A. (2017) · Scientific Reports · doi:10.1038/s41598-017-03183-0 · Cited by 29 · see citing works

Maternal exposure to smoking and infant's wheeze and asthma: Japan Environment and Children's Study

Wada, T., Adachi, Y., Murakami, S., Ito, Y., Itazawa, T., Tsuchida, A., Matsumura, K., Hamazaki, K., Inadera, H., Kamijima, M., et al. (2021) · Allergology International · doi:10.1016/j.alit.2021.04.008 · Cited by 29 · see citing works

The effects of ambient temperature on outpatient visits for varicella and herpes zoster in Shanghai, China: A time-series study

Yang, Y., Chen, R., Xu, J., Li, Q., Xu, X., Ha, S., Song, W., Tan, J., Xu, F., & Kan, H. (2015) · Journal of the American Academy of Dermatology · doi:10.1016/j.jaad.2015.07.015 · Cited by 28 · see citing works

Immune checkpoint inhibitors for the treatment of sepsis:insights from preclinical and clinical development

Rienzo, M., Skirecki, T., Monneret, G., & Timsit, J. (2022) · Expert Opinion on Investigational Drugs · doi:10.1080/13543784.2022.2102477 · Cited by 28 · see citing works

Arsenic exposure and serum antibody concentrations to diphtheria and tetanus toxoid in children at age 5: A prospective birth cohort in Bangladesh

Welch, B. M., Branscum, A. J., Ahmed, S. M., Hystad, P., Smit, E., Afroz, S., Megowan, M. R., Mostofa, G., Hasan, M. O. S. I., Rahman, M. L., et al. (2019) · Environment International · doi:10.1016/j.envint.2019.04.015 · Cited by 28 · see citing works

Association between Peripheral Inflammatory Cytokines and Cognitive Function in Patients with First-Episode Schizophrenia

Baek, S.-H., Kim, H., Kim, J., Ryu, S., Lee, J., Kim, J., Shin, I., & Kim, S. (2022) · Journal of Personalized Medicine · doi:10.3390/jpm12071137 · Cited by 28 · see citing works

The effects of aflatoxin exposure on Hepatitis B-vaccine induced immunity in Kenyan children

Githanga, D. P., Dixon, R. W., Mw, M., Wandiga, S. O., Mutegi, C., Ogutu, B. R., Agweyu, A., Wang, J.-S., & Anzala, O. A. (2019) · Current problems in pediatric and adolescent health care · doi:10.1016/j.cppeds.2019.04.005 · Cited by 26 · see citing works

Association of Maternal Influenza Vaccination During Pregnancy With Early Childhood Health Outcomes

Mehrabadi, A., Dodds, L. A., MacDonald, N. E., Top, K. A., Benchimol, E. I., Kwong, J. C., Ortiz, J. R., Sprague, A. E., Walsh, L. K., Wilson, K. R., et al. (2021) · JAMA · doi:10.1001/jama.2021.6778 · Cited by 26 · see citing works

Understanding the Ontogeny of the Immune System to Promote Immune-Mediated Health for Life

Marchant, A., & Kollmann, T. R. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00077 · Cited by 26 · see citing works

Revolutionizing adjuvant development: harnessing AI for next-generation cancer vaccines

Zhang, W., Zheng, X., Coghi, P. S., Chen, J.-H., Dong, B.-J., & Fan, X. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1438030 · Cited by 27 · see citing works

From Womb to Mind: Prenatal Epigenetic Influences on Mental Health Disorders

Álvarez-Mejía, D., Rodas, J. A., & León-Rojas, J. E. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26136096 · Cited by 30 · see citing works

Evaluation of nutritional status in pediatric patients diagnosed with Covid-19 infection

Molla, G. K., Uzun, Ö. Ü., Koç, N., Yeşil, B. Ö., & Bayhan, G. İ. (2021) · Clinical Nutrition ESPEN · doi:10.1016/j.clnesp.2021.04.022 · Cited by 25 · see citing works

Poverty and Relapse Risk in Children with Acute Lymphoblastic Leukemia: Children's Oncology Group Study AALL03N1 Report

Wadhwa, A., Chen, Y., Hageman, L., Hoppmann, A. L., Angiolillo, A. L., Dickens, D. S., Neglia, J. P., Ravindranath, Y., Ritchey, K., Termuhlen, A. M., et al. (2023) · Blood · doi:10.1182/blood.2023019631 · Cited by 23 · see citing works

Interaction between gut microbiota and immunity in health and intestinal disease

Wang, Q., Meng, Q., Chen, Y., Liu, Y., Li, X., Zhou, J., Ma, Y., Yu, Z., & Chen, X. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1673852 · Cited by 27 · see citing works

The role of incretins and incretin-based drugs in autoimmune diseases

Radbakhsh, S., Atkin, S. L., Simental‐Mendía, L. E., & Sahebkar, A. (2021) · International Immunopharmacology · doi:10.1016/j.intimp.2021.107845 · Cited by 24 · see citing works

COVID-19 ‘asymptomatic’ patients: an old wives’ tale

Mouliou, D. S., & Gourgoulianis, K. I. (2022) · Expert Review of Respiratory Medicine · doi:10.1080/17476348.2022.2030224 · Cited by 22 · see citing works

A chromosome-level genome assembly and intestinal transcriptome of Trypoxylus dichotomus (Coleoptera: Scarabaeidae) to understand its lignocellulose digestion ability

Wang, Q., Liu, L., Zhang, S., Wu, H., & Huang, J. (2022) · GigaScience · doi:10.1093/gigascience/giac059 · Cited by 22 · see citing works

Plasmodium falciparum and Helminth Coinfections Increase IgE and Parasite-Specific IgG Responses

Santano, R., Rubio, R., Grau-Pujol, B., Escola, V., Muchisse, O., Cuamba, I., Vidal, M., Cisteró, P., Ruiz-Olalla, G., Aguilar, R., et al. (2021) · Microbiology Spectrum · doi:10.1128/spectrum.01109-21 · Cited by 20 · see citing works

Interleukin ‐1α and tumor necrosis factor α as an inducer for reactive‐oxygen‐species‐mediated NOD‐like receptor protein 1/NOD‐like receptor protein 3 inflammasome activation in mononuclear blood cells from individuals with chronic insomnia disorder

Aghelan, Z., Karima, S., Khazaie, H., Abtahi, S. H., Farokhi, A., Rostampour, M., Bahrehmand, F., & Khodarahmi, R. (2022) · European Journal of Neurology · doi:10.1111/ene.15540 · Cited by 20 · see citing works

Prenatal exposure to TCDD and atopic conditions in the Seveso second generation: a prospective cohort study

Ye, M., Warner, M., Mocarelli, P., Brambilla, P., & Eskenazi, B. (2018) · Environmental Health · doi:10.1186/s12940-018-0365-2 · Cited by 20 · see citing works

Pattern of antibody responses to Plasmodium falciparum antigens in individuals differentially exposed to Anopheles bites

Aka, K. G., Traoré, D. F., Sagna, A. B., Zoh, D. D., Assi, S.-B., Tchiekoi, B. N., Adja, A. M., Remoué, F., & Poinsignon, A. (2020) · Malaria Journal · doi:10.1186/s12936-020-03160-5 · Cited by 20 · see citing works

Immune Checkpoint Inhibitors and the Exposome: Host-Extrinsic Factors Determine Response, Survival, and Toxicity

Pizzutilo, E. G., Romanò, R., Roazzi, L., Agostara, A. G., Oresti, S., Zeppellini, A., Giannetta, L. G., Cerea, G., Signorelli, D., Siena, S., et al. (2023) · Cancer Research · doi:10.1158/0008-5472.can-23-0161 · Cited by 19 · see citing works

Increased T Cell Differentiation and Cytolytic Function in Bangladeshi Compared to American Children

Wagar, L. E., Bolen, C. R., Sigal, N., Angel, C. J. L., Guan, L., Kirkpatrick, B. D., Haque, R., Tibshirani, R. J., Parsonnet, J., Petri, W. A., et al. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02239 · Cited by 19 · see citing works

Early immune stimulation and childhood acute lymphoblastic leukemia in Costa Rica: A comparison of statistical approaches

Figueroa, S. C., Kennedy, C. J., Wesseling, C., Wiemels, J., Morimoto, L. M., & Mora, A. M. (2019) · Environmental Research · doi:10.1016/j.envres.2019.109023 · Cited by 18 · see citing works

Identification of modifiable pre- and postnatal dietary and environmental exposures associated with owner-reported canine atopic dermatitis in Finland using a web-based questionnaire

Hemida, M. B. M., Vuori, K. A. M., Salin, S., Moore, R., Anturaniemi, J., & Hielm-Björkman, A. K. (2020) · PLoS ONE · doi:10.1371/journal.pone.0225675 · Cited by 18 · see citing works

Health Outcomes in Young Children Following Pertussis Vaccination During Pregnancy

Laverty, M., Crowcroft, N. S., Bolotin, S., Hawken, S., Wilson, K. R., Amirthalingam, G., Biringer, A. B., Cook, J. L., Dubey, V., Fakhraei, R., et al. (2021) · PEDIATRICS · doi:10.1542/peds.2020-042507 · Cited by 18 · see citing works

Suicide and Inflammation

Donegan, J. J., & Nemeroff, C. B. (2023) · Advances in experimental medicine and biology · doi:10.1007/978-981-19-7376-5_17 · Cited by 18 · see citing works

A lifetime perspective on risk factors for cognitive decline with a special focus on early events

Kuhn, H. G., Skau, S., & Nyberg, J. (2024) · Cerebral Circulation - Cognition and Behavior · doi:10.1016/j.cccb.2024.100217 · Cited by 20 · see citing works

Immunological considerations regarding parental concerns on pediatric immunizations

Nicoli, F., & Appay, V. (2017) · Vaccine · doi:10.1016/j.vaccine.2017.04.030 · Cited by 17 · see citing works

Interpretation of the hygiene and microflora hypothesis for allergic diseases through epigenetic epidemiology

Bae, J. (2018) · Epidemiology and Health · doi:10.4178/epih.e2018006 · Cited by 16 · see citing works

Topic modeling of major research themes in disease ecology of mammals

Han, B. A., & Ostfeld, R. S. (2018) · Journal of Mammalogy · doi:10.1093/jmammal/gyy174 · Cited by 16 · see citing works

Prenatal and childhood exposure to phthalic acid esters and vaccination antibodies in children: A 15-year follow-up birth cohort study

Wen, H., Guo, Y. L., Su, P., Sun, C.-W., & Wang, S. (2020) · Environment International · doi:10.1016/j.envint.2020.106134 · Cited by 16 · see citing works

Neonate-omics: Charting the Unknown Immune Response in Early Life

Jennewein, M. F., Butler, A. L., & Alter, G. (2018) · Cell · doi:10.1016/j.cell.2018.08.001 · Cited by 16 · see citing works

Characterization of CD 127− CD 25++ Treg from human colostrum

Cérbulo‐Vázquez, A., Hernández‐Peláez, G., Arriaga‐Pizano, L., Bautista‐Pérez, P., Romero‐Venado, J., Flores‐González, J., Figueroa-Damián, R., Soriano-Becerril, D. M., & Mancilla‐Herrera, I. (2017) · American Journal of Reproductive Immunology · doi:10.1111/aji.12806 · Cited by 15 · see citing works

Domestication shapes the pig gut microbiome and immune traits from the scale of lineage to population

Kuthyar, S., Diaz, J., Avalos-Villatoro, F., Maltecca, C., Tiezzi, F., Dunn, R. R., & Reese, A. T. (2023) · Journal of Evolutionary Biology · doi:10.1111/jeb.14227 · Cited by 14 · see citing works

Immunomodulatory Effects of Vitamin D Supplementation in a Deficient Population

Garand, M., Toufiq, M., Singh, P., Huang, S. S. Y., Tomei, S., Mathew, R., Mattei, V., Alwakeel, M., Sharif, E., & Khodor, S. A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22095041 · Cited by 16 · see citing works

A cross-section study of the comparison of plasma inflammatory cytokines and short-chain fatty acid in patients with depression and schizophrenia

Yu, H., Li, R., Liang, X., Yang, W., Guo, L., Liu, L., Tan, Q., & Peng, Z. (2024) · BMC Psychiatry · doi:10.1186/s12888-024-06277-y · Cited by 14 · see citing works

Challenges of Immune Response Diversity in the Human Population Concerning New Tuberculosis Diagnostics, Therapies, and Vaccines

Azad, A. K., Lloyd, C., Sadée, W., & Schlesinger, L. S. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.00139 · Cited by 12 · see citing works

Salient Conclusive Remarks on Epidemiology and Clinical Manifestations of Pediatric COVID-19: Narrative Review

Ali, A. S., Al-Hakami, A. M., Shati, A. A., Asseri, A. A., & Al-Qahatani, S. M. (2020) · Frontiers in Pediatrics · doi:10.3389/fped.2020.584694 · Cited by 13 · see citing works

Differential Microglial Morphological Response, TNFα, and Viral Load in Sedentary-like and Active Murine Models After Systemic Non-neurotropic Dengue Virus Infection

Gomes, G. F., Peixoto, R. D. D. F., Maciel, B. G., dos Santos, K. F., Bayma, L. R., Neto, P. A. F., Fernandes, T. N., de Abreu, C. C., Casseb, S. M. M., de Lima, C. M., et al. (2019) · Journal of Histochemistry & Cytochemistry · doi:10.1369/0022155419835218 · Cited by 13 · see citing works

Biology and Natural History of Type 1 Diabetes Mellitus

Fernandes, T. A. A. D. M., de Azevedo, J. C. V., Cavalcante, G. A., de Medeiros, I. A. C. M., Lanza, D. C. F., de Araújo, J. M. G., Bezerra, F. L., & Fernandes, J. V. (2022) · Current Pediatric Reviews · doi:10.2174/1573396318666220409001955 · Cited by 13 · see citing works

B cell receptor-induced IL-10 production from neonatal mouse CD19+CD43- cells depends on STAT5-mediated IL-6 secretion

Sakai, J., Yang, J., Chou, C.-K., Wu, W. W., & Akkoyunlu, M. (2023) · eLife · doi:10.7554/elife.83561 · Cited by 9 · see citing works

DNA methylome profiling of blood to identify individuals in a pair of monozygotic twins

Kim, J. J., Lee, H. Y., Lee, S.-Y., Kim, S., Park, J., & Lee, S. D. (2023) · Genes & Genomics · doi:10.1007/s13258-023-01396-4 · Cited by 12 · see citing works

Gut microbiota and immunity in health and diseases: a review

Okolie, M. C., Edo, G. I., Ainyanbhor, I. E., Jikah, A. N., Akpoghelie, P. O., Yousif, E. A., Zainulabdeen, K., Isoje, E. F., Igbuku, U. A., Orogu, J. O., et al. (2024) · Proceedings of the Indian National Science Academy · doi:10.1007/s43538-024-00355-1 · Cited by 12 · see citing works

Assessing the safety of bioactive ingredients in infant formula that affect the immune system: recommendations from an expert panel

Callahan, E. A., Chatila, T. A., Deckelbaum, R. J., Field, C. J., Greer, F. R., Hernell, O., Järvinen, K. M., Kleinman, R. E., Milner, J. D., Neu, J., et al. (2021) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/nqab346 · Cited by 12 · see citing works

The DBL-1/TGF-β signaling pathway tailors behavioral and molecular host responses to a variety of bacteria in Caenorhabditis elegans

Madhu, B., Lakdawala, M. F., & Gumienny, T. L. (2023) · eLife · doi:10.7554/elife.75831 · Cited by 12 · see citing works

Diet and Hygiene in Modulating Autoimmunity During the Pandemic Era

Abdelhamid, L., & Luo, X. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2021.749774 · Cited by 12 · see citing works

Infants' diminished response to DTaP vaccine is associated with exposure to organophosphate esters

Hammel, S. C., Nordone, S. K., Zhang, S., Lorenzo, A., Eichner, B., Moody, M. A., Harrington, L., Gandee, J., Schmidt, L., Smith, S. G., et al. (2022) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2022.155782 · Cited by 12 · see citing works

High-dimensional single cell mass cytometry analysis of the murine hematopoietic system reveals signatures induced by ageing and physiological pathogen challenges

Nikolaou, C., Mühle, K., Schlickeiser, S., Japp, A. S., Matzmohr, N., Kunkel, D., Frentsch, M., & Thiel, A. (2021) · Immunity & Ageing · doi:10.1186/s12979-021-00230-3 · Cited by 11 · see citing works

Whole-genome sequencing provides novel insights into the evolutionary history and genetic adaptation of reindeer populations in northern Eurasia

Pokharel, K., Weldenegodguad, M., Dudeck, S., Honkatukia, M., Lindeberg, H., Mazzullo, N., Paasivaara, A., Peippo, J., Soppela, P., Stammler, F., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-50253-7 · Cited by 10 · see citing works

Moving toward improved immune checkpoint immunotherapy for advanced prostate cancer

Velasco, M. A. D., Kura, Y., Fujita, K., & Uemura, H. (2024) · International Journal of Urology · doi:10.1111/iju.15378 · Cited by 10 · see citing works

The effect of whole blood logistics on neutrophil non-specific activation and kinetics ex vivo

Li, C., Farooqui, M. A., Yada, R. C., Cai, J. B., Anna Huttenlocher, A., & Beebe, D. J. (2024) · Scientific Reports · doi:10.1038/s41598-023-50813-x · Cited by 10 · see citing works

Alginate-based bionanocomposites in wound dressings

Radoor, S., Karayil, J., Jayakumar, A., Radhakrishnan, E. K., Parameswaranpillai, J., & Siengchin, S. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-821280-6.00003-9 · Cited by 10 · see citing works

SARS-CoV 2 (Covid-19) Heterogeneous Mortality Rates across Countries May Be Partly Explained by Life Expectancy, Calorie Intake, and Prevalence of Diabetes.

Nkhata, S. G., Ngoma, T. N., & Chilenga, P. M. (2020) · Human Ecology · doi:10.1007/s10745-020-00191-z · Cited by 9 · see citing works

Molecular and Epigenetics Mechanisms for the Immune Control of Plasmodium Parasites Infection: A Comprehensive Review

Adejoh, J., Madu, C., Egua, M. O., Alli, L. A., Raheem, D., & Okoh, M. P. (2023) · Asian Journal of Biological Sciences · doi:10.3923/ajbs.2023.636.669 · Cited by 8 · see citing works

Association between Meteorological Factors and Outpatient Visits for Herpes Zoster in Hefei, China: A Time-Series Analysis

Lv, X.-J., Fang, X., Qian, T.-T., Cai, Y.-Y., Gao, P., Chen, H., Wu, Q., Wu, J., Fan, Y., & Ye, D. (2023) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph20032097 · Cited by 8 · see citing works

On developmental programming of the immune system

Hong, J. Y., & Medzhitov, R. M. (2023) · Trends in Immunology · doi:10.1016/j.it.2023.09.004 · Cited by 30 · see citing works

Postnatal Innate Immune Development: From Birth to Adulthood

Georgountzou, A., & Papadopoulos, N. G. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00957 · Cited by 204 · see citing works

Influence of Early-Life Environmental Exposures on Immune Function Across the Life Span

Boulé, L. A., & Lawrence, B. P. (2016) · Springer eBooks · doi:10.1007/978-3-7091-1890-0_2 · Cited by 12 · see citing works

How do environmental factors shape immune function in vertebrates

Bontekoe, I. D. (2018)

Immune development in early life

Palma, P., Färber, D. L., Konnikova, L., & Levy, O. (2026) · Nature Immunology · doi:10.1038/s41590-026-02523-5 · Cited by 10 · see citing works