Neonatal measles immunity in rural Kenya: the influence of HIV and placental malaria infections on placental transfer of antibodies and levels of antibody in maternal and cord serum samples

Scott, Susana; Cumberland, Phillippa; Shulman, Caroline E.; Cousens, Simon; Cohen, Bernard J.; Brown, David W. G.; Bulmer, Judith N.; Dorman, Edgar K.; Kawuondo, Ken; Marsh, Kevin; Cutts, Felicity

doi:10.1086/429963

Cited by 117Virology and Viral DiseasesVaccine Coverage and HesitancyHIV/AIDS Research and Interventions

Neonatal measles immunity in rural Kenya: the influence of HIV and placental malaria infections on placental transfer of antibodies and levels of antibody in maternal and cord serum samples

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Scott, Susana, Cumberland, Phillippa, Shulman, Caroline E., Cousens, Simon, Cohen, Bernard J., Brown, David W. G., Bulmer, Judith N., Dorman, Edgar K. +3 more·2005·The Journal of Infectious Diseases

DOI 10.1086/429963

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Abstract

INTRODUCTION: Young infants are protected from measles infection by maternal measles antibodies. The level of these antibodies at birth depends on the level of antibodies in the mother and the extent of placental transfer. We investigated predictors of levels of measles antibodies in newborns in rural Kenya. METHODS: A total of 747 paired maternal-cord serum samples (91 from human immunodeficiency virus [HIV]-infected and 656 from HIV-uninfected mothers) were tested for measles immunoglobulin G antibodies. Placental malaria infection was determined by biopsy. Data on pregnancy history, gestational age, and anthropometric and socioeconomic status were collected. RESULTS: Infants born to HIV-infected mothers were more likely (odds ratio, 4.6 [95% confidence interval {CI}, 2.2-9.7]) to be seronegative and had 35.1% (95% CI, 9.8%-53.2%) lower levels of measles antibodies than did those born to HIV-uninfected mothers. Preterm delivery, early maternal age, and ethnic group were also associated with reduced levels of measles antibodies. There was little evidence that placental malaria infection was associated with levels of measles antibodies in newborns. CONCLUSION: Our results suggest that maternal HIV infection may reduce levels of measles antibodies in newborns. Low levels of measles antibodies at birth render children susceptible to measles infection at an early age. This is of concern in sub-Saharan African countries, where not only is the prevalence of HIV high, but measles is the cause of much morbidity and mortality.

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Maternal chronic infection can reduce the transplacental transfer of IgG specific to RSV, measles, tetanus, and HiB.
“It is now well established that maternal chronic infection can reduce the transplacental transfer of IgG specific to a variety of important childhood pathogens, including RSV, measles, tetanus, and HiB (37, 99–103).”
From Factors Affecting the FcRn-Mediated Transplacental Transfer of Antibodies and Implications for Vaccination in Pregnancy (2017) · cites this paper as [102]

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Placental transport of immunoglobulin G
Simister, N. (2003) · Vaccine · doi:10.1016/s0264-410x(03)00334-7 · Cited by 783 · see citing works
Intermittent sulphadoxine-pyrimethamine to prevent severe anaemia secondary to malaria in pregnancy: a randomised placebo-controlled trial
Shulman, C. E., Dorman, E. K., Cutts, F. T., Kawuondo, K., Bulmer, J. N., Peshu, N. M., & Marsh, K. (1999) · The Lancet · doi:10.1016/s0140-6736(98)07318-8 · Cited by 386 · see citing works
Self-citation
Mechanisms of hypergammaglobulinemia and impaired antigen-specific humoral immunity in HIV-1 infection
Milito, A. D., Nilsson, A., Titanji, K., Thorstensson, R., Reizenstein, E., Narita, M., Grützmeier, S., Sönnerborg, A. B., & Chiodi, F. (2003) · Blood · doi:10.1182/blood-2003-07-2375 · Cited by 311 · 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
Malaria in pregnancy: adverse effects on haemoglobin levels and birthweight in primigravidae and multigravidae
Shulman, C. E., Marshall, T., Dorman, E. K., Bulmer, J. N., Cutts, F., Peshu, N., & Marsh, K. (2001) · Tropical Medicine & International Health · doi:10.1046/j.1365-3156.2001.00786.x · Cited by 182 · see citing works
Self-citation
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
HIV prevalence and trends in sub-Saharan Africa: no decline and large subregional differences
Asamoah-Odei, E., Calleja, J. M. G., & Boerma, J. T. (2004) · The Lancet · doi:10.1016/s0140-6736(04)16587-2 · Cited by 151 · see citing works
The human materno-foetal relationship in malaria. II. Histological, ultrastructural and immunopathological studies of the placenta
Galbraith, R. M., Fox, H., Hsi, B., Galbraith, G. M. P., Bray, R. S., & Faulk, W. P. (1980) · Transactions of the Royal Society of Tropical Medicine and Hygiene · doi:10.1016/0035-9203(80)90012-7 · Cited by 131 · see citing works
Transfer of Measles, Mumps, and Rubella Antibodies From Mother to Infant
Sato, H. (1979) · American journal of diseases of children · doi:10.1001/archpedi.1979.02130120032005 · Cited by 126 · 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
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
Maternally derived measles immunity in era of vaccine-protected mothers
Lennon, J. L., & Black, F. L. (1986) · The Journal of Pediatrics · doi:10.1016/s0022-3476(86)81039-3 · Cited by 113 · see citing works
Influence of Maternal Antibodies on Neonatal Immunization against Respiratory Viruses
Crowe, J. E. (2001) · Clinical Infectious Diseases · doi:10.1086/322971 · Cited by 111 · see citing works
Changing levels of measles antibody titers in women and children in the United States: impact on response to vaccination. Kaiser Permanente Measles Vaccine Trial Team.
Markowitz, L. E., Albrecht, P., Rhodes, P., Demonteverde, R., Swint, E. B., Maes, E. F., Powell, C. J., & Patriarca, P. A. (1996) · PubMed · Cited by 97 · see citing works
GEOGRAPHIC VARIATION IN INFANT LOSS OF MATERNAL MEASLES ANTIBODY AND IN PREVALENCE OF RUBELLA ANTIBODY
Black, F. L., Berman, L. L., Borgono, J. M., Capper, R. A., de Carvalho, A. A., COLLINS, C., GLOVER, O., Hijazi, Z. M., Jacobson, D. L., Lee, Y.-L., et al. (1986) · American Journal of Epidemiology · doi:10.1093/oxfordjournals.aje.a114415 · Cited by 96 · see citing works
Reduced measles immunity in infants in a well-vaccinated population
Pabst, H. F., Spady, D. W., MARUSYK, R. G., Carson, M. M., Chui, L., Joffres, M. R., & GRIMSRUD, K. M. (1992) · The Pediatric Infectious Disease Journal · doi:10.1097/00006454-199207000-00004 · Cited by 90 · see citing works
Untitled work
(2001) · PubMed · Cited by 73 · see citing works
Transplacental transfer of measles and total IgG
GONÇALVES, G., CUTTS, F. T., HILLS, M., REBELO-ANDRADE, H., TRIGO, F. A., & BARROS, H. (1999) · Epidemiology and Infection · doi:10.1017/s0950268899002046 · Cited by 60 · see citing works
Self-citation
A study of maternally derived measles antibody in infants born to naturally infected and vaccinated women
Brugha, R., Ramsay, M. E., Forsey, T., & Brown, D. (1996) · Epidemiology and Infection · doi:10.1017/s0950268800059203 · Cited by 60 · see citing works
Self-citation
The influence of prematurity and low birthweight on transplacental antibody transfer in a rural West African population
Okoko, J. B., Wesumperuma, H. L., & Hart, C. A. (2001) · Tropical Medicine & International Health · doi:10.1046/j.1365-3156.2001.00741.x · Cited by 59 · see citing works
The influence of prematurity and low birthweight on transplacental antibody transfer in Sri Lanka
Wesumperuma, H. L. (1999) · Annals of Tropical Medicine and Parasitology · doi:10.1080/00034989958654 · Cited by 49 · see citing works
Maternally acquired immunity in newborns from women infected by the human immunodeficiency virus
de Moraes‐Pinto, M. I., Farhat, C., Carbonare, S. B., Curti, S., Otsubo, M., Lazarotti, D. S., Campagnoli, R., & Carneiro-Sampaio, M. M. S. (1993) · Acta Paediatrica · doi:10.1111/j.1651-2227.1993.tb12805.x · Cited by 45 · see citing works
Placental transfer of measles antibodies: effect of gestational age and maternal vaccination status
Linder, N., Tallen-Gozani, E., German, B., Duvdevani, P., Ferber, A., & Sirota, L. (2003) · Vaccine · doi:10.1016/j.vaccine.2003.10.009 · Cited by 41 · see citing works
Passive immunity against measles during the first 8 months of life of infants born to vaccinated mothers or to mothers who sustained measles
Serres, G. D., Joly, J. R., Fauvel, M., Meyer, F., Mâsse, B. R., & Boulianne, N. (1997) · Vaccine · doi:10.1016/s0264-410x(96)00283-6 · Cited by 35 · see citing works
The influence of prematurity and low birthweight on transplacental antibody transfer in Sri Lanka
Wesumperuma, H. L., Perera, A., Pharoah, P. O. D., et al. (1999) · Annals of Tropical Medicine and Parasitology · doi:10.1080/00034983.1999.11813407 · Cited by 34 · see citing works
Placental Transfer of Tetanus Antibodies and Protection of the Newborn
Gendrel, D., Richard-Lenoble, D., Massamba, M., Picaud, A., Francoual, C., & Blot, P. (1990) · Journal of Tropical Pediatrics · doi:10.1093/tropej/36.6.279 · Cited by 32 · see citing works
Optimal age for vaccination against measles in the State of São Paulo, Brazil, taking into account the mother’s serostatus
Zanetta, R. A. C., Amaku, M., Azevedo, R. S., Zanetta, D. M. T., Burattini, M. N., & Massad, E. (2001) · Vaccine · doi:10.1016/s0264-410x(01)00267-5 · Cited by 30 · see citing works
Measles antibodies in women and infants in the vaccine era.
Kacica, M. A., Hughes, P. A., LEPOW, M. L., Venzia, R. A., & Miller, J. D. (1995) · Journal of Medical Virology · doi:10.1002/jmv.1890450220 · Cited by 29 · see citing works
[MEASLES AND MEASLES VACCINE].
Sans-Sabrafen, J. (1964) · PubMed · Cited by 24 · see citing works
A SIMPLIFIED METHOD OF ESTIMATING GESTATIONAL AGE IN AN AFRICAN POPULATION
Eregie, C. O., & Muogbo, D. C. (1991) · Developmental Medicine & Child Neurology · doi:10.1111/j.1469-8749.1991.tb05093.x · Cited by 16 · see citing works
Reduced transfer of tetanus antibodies with placental malaria
Brair, M. ‐., Brabin, B. J., Milligan, P. J., Maxwell, S., & Hart, C. A. (1994) · International Journal of Gynecology & Obstetrics · doi:10.1016/0020-7292(94)90496-0 · Cited by 12 · see citing works
Durability of Passive Measles Antibody in Jamaican Children
Christie, C. D. C., LEE-HIRSH, J., ROGALL, B., MERRILL, S., Ramlal, A. M., Karian, V. E., & Black, F. L. (1990) · International Journal of Epidemiology · doi:10.1093/ije/19.3.698 · Cited by 11 · see citing works
Transplacentally transmitted anti-measles antibodies in term and preterm infants.
Rau, A., Dhulia, A., Wilson, C. G., Chopra, G., & Sarkar, P. K. (2002) · PubMed · Cited by 9 · see citing works
Transplacental transfer of measles antibody in Delhi.
Singh, J. K., Khare, S., Prabha, S., Chandra, R., Dc, J., Bhatia, R., & Sokhey, J. (1998) · PubMed · Cited by 5 · see citing works
Maternal and cord blood measles antibody titres.
Kaur, G., Dk, A., Gulati, A. K., Kalra, A., Gp, K., & Kn, A. (1982) · PubMed · Cited by 4 · see citing works
Largest ever measles vaccination programme launched in Africa
Siringi, S. (2002) · The Lancet · doi:10.1016/s0140-6736(02)09193-6 · Cited by 3 · see citing works
Africa's largest measles vaccination campaign could reduce childhood mortality by 20%.
Wanyama, C. (2002) · PubMed · doi:10.1590/s0042-96862002001200021 · Cited by 3 · see citing works
Measles Elimination in Mexico
(2004) · PsycEXTRA Dataset · doi:10.1037/e520842010-004 · Cited by 2 · see citing works

Flagged first, then by citations

Research works printed but not linked: 5

[2]2. World Health Organization. Global measles mortality reduction and regional elimination, 2000-2001. Part 1. Wkly Epidemiol Rec 2002; 7: 50-5.
[12]12. Lepage P, Dabis F, Msellati P, et al. Safety and immnunogenicity of high-dose Edmonston-Zagreb measles vaccine in children with HIV- 1 infection. Am J Dis Child 1992; 146:550-5.
[16]16. Markowitz LE, Albrecht P, Rhodes P, et al. Changing levels of measles antibody titers in women and children in the United States: impact on response to vaccination. Pediatrics 1996; 97:53-8.
[31]31. WHO/UNICEF Review of National Immunization Coverage 1980- 2003. Kenya. Available at: http://www.childinfo.org/eddb/immuni/ africa/Kenya_2003_final.pdf. Accessed 5 December 2004.
[39]39. Ministry of Health of Kenya, World Health Organization. Measles im- munity in the first year after birth and the optimum age for vaccination in Kenyan children. Bull World Health Organ 1977; 55:21-30.

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Palmeira, P., Quinello, C., Silveira-Lessa, A. L., Zago, C. A., & Carneiro-Sampaio, M. (2012) · Clinical and Developmental Immunology · doi:10.1155/2012/985646 · Cited by 1,037 · see citing works
Low birth weight: Case definition & guidelines for data collection, analysis, and presentation of maternal immunization safety data
Cutland, C., Lackritz, E., Moore, T. M., Bardají, A., Chandrasekaran, R., Lahariya, C., Nisar, M. I., Tapia, M. D., Pathirana, J. C., Kochhar, S., et al. (2017) · Vaccine · doi:10.1016/j.vaccine.2017.01.049 · Cited by 460 · see citing works
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Human Immunology of Measles Virus Infection
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Atwell, J. E., Thumar, B., Robinson, L. J., Tobby, R., Yambo, P., Ome-Kaius, M., Siba, P. M., Unger, H. W., Rogerson, S. J., King, C. L., et al. (2016) · Journal of Infectious Diseases · doi:10.1093/infdis/jiv401 · Cited by 48 · see citing works
Drivers of vaccine decision-making in South Africa: A discrete choice experiment
Verelst, F., Kessels, R., Delva, W., Beutels, P., & Willem, L. (2019) · Vaccine · doi:10.1016/j.vaccine.2019.02.056 · Cited by 49 · see citing works
Biological factors that may impair transplacental transfer of RSV antibodies: Implications for maternal immunization policy and research priorities for low- and middle-income countries
Atwell, J. E., Lutz, C. S., Sparrow, E. G., & Feikin, D. R. (2022) · Vaccine · doi:10.1016/j.vaccine.2022.06.034 · Cited by 44 · see citing works
Effect of in-utero HIV exposure and antiretroviral treatment strategies on measles susceptibility and immunogenicity of measles vaccine
Simani, O. E., Adrian, P. V., Violari, A., Kuwanda, L., Otwombe, K. N., Nunes, M. C., Cotton, M. F., & Madhi, S. A. (2013) · AIDS · doi:10.1097/qad.0b013e32835fae26 · Cited by 42 · see citing works
Placental Malaria: Decreased Transfer of Maternal Antibodies Directed to Plasmodium falciparum and Impact on the Incidence of Febrile Infections in Infants
Dechavanne, C., Cottrell, G., Garcia, A., & Migot-Nabias, F. (2015) · PLOS ONE · doi:10.1371/journal.pone.0145464 · Cited by 42 · see citing works
Malaria and HIV Infection in Mozambican Pregnant Women Are Associated With Reduced Transfer of Antimalarial Antibodies to Their Newborns
Moro, L., Bardají, A., Nhampossa, T., Mandomando, I., Serra‐Casas, E., Sigaúque, B., Cisteró, P., Chauhan, V. S., Chitnis, C. E., Ordï, J., et al. (2014) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiu547 · Cited by 40 · see citing works
Specific antibodies against vaccine-preventable infections: a mother–infant cohort study
Jones, C. E., Pollock, L., Barnett, S. M., Battersby, A., & Kampmann, B. (2013) · BMJ Open · doi:10.1136/bmjopen-2012-002473 · Cited by 39 · see citing works
Placental malaria, maternal HIV infection and infant morbidity
Briand, V., Badaut, C., & Cot, M. (2009) · Annals of Tropical Paediatrics · doi:10.1179/146532809x440699 · Cited by 39 · see citing works
Persistence of Vaccine-Induced Measles Antibody Beyond Age 12 Months: A Comparison of Response to One and Two Doses of Edmonston-Zagreb Measles Vaccine Among HIV-Infected and Uninfected Children in Malawi
Fowlkes, A. L., Witte, D., Beeler, J. A., Audet, S. A., Garcia, P., Curns, A. T., Yang, C., Fudzulani, R., Broadhead, R., Bellini, W. J., et al. (2011) · The Journal of Infectious Diseases · doi:10.1093/infdis/jir135 · Cited by 35 · see citing works
Self-citation
Malaria in pregnancy shapes the development of foetal and infant immunity
Harrington, W. E., Kakuru, A., & Jagannathan, P. (2019) · Parasite Immunology · doi:10.1111/pim.12573 · Cited by 35 · see citing works
Predicted impact of the HIV-1 epidemic on measles in developing countries: results from a dynamic age-structured model
Scott, S., Mossong, J., Moss, W. J., Cutts, F. T., & Cousens, S. N. (2008) · International Journal of Epidemiology · doi:10.1093/ije/dyn007 · Cited by 34 · see citing works
Self-citation
Suppression of circulating IgD+CD27+ memory B cells in infants living in a malaria-endemic region of Kenya
Asito, A. S., Piriou, E., Jura, W. G. Z. O., Ouma, C., Odada, P. S., Ogola, S., Fiore, N. C., & Rochford, R. A. (2011) · Malaria Journal · doi:10.1186/1475-2875-10-362 · Cited by 34 · see citing works
Maternal pneumococcal capsular IgG antibodies and transplacental transfer are low in South Asian HIV-infected mother-infant pairs
Gupta, A., Mathad, J. S., Yang, W.-T., Singh, H. K., Gupte, N., Mave, V., Bharadwaj, R. S., Zaman, K., Roy, E., Bollinger, R. C., et al. (2014) · Vaccine · doi:10.1016/j.vaccine.2014.01.033 · Cited by 33 · see citing works
Reduced Transplacental Transfer of a Subset of Epstein-Barr Virus-Specific Antibodies to Neonates of Mothers Infected with Plasmodium falciparum Malaria during Pregnancy
Ogolla, S., Daud, I. I., Asito, A. S., Sumba, O. P., Ouma, C., VULULE, J. M., Middeldorp, J. M., Dent, A. E., Mehta, S., & Rochford, R. A. (2015) · Clinical and Vaccine Immunology · doi:10.1128/cvi.00270-15 · Cited by 31 · see citing works
Measles vaccine
Strebel, P. M., Papania, M. J., Fiebelkorn, A. P., & Halsey, N. A. (2013) · Elsevier eBooks · doi:10.1016/b978-1-4557-0090-5.00028-8 · Cited by 31 · see citing works
Incidence and Risk Factors for Neonatal Tetanus in Admissions to Kilifi County Hospital, Kenya
Ibinda, F., Bauni, E., Kariuki, S. M., Fegan, G., Lewa, J. D., Mwikamba, M., Boga, M., Odhiambo, R., Mwagandi, K., Seale, A. C., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0122606 · Cited by 30 · see citing works
The transfer and decay of maternal antibodies against enterovirus A71, and dynamics of antibodies due to later natural infections in Chinese infants: a longitudinal, paired mother–neonate cohort study
Wei, X., Yang, J., Gao, L., Wang, L., Liao, Q., Qiu, Q., Luo, K., Yu, S., Zhou, Y., Liu, F., et al. (2020) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(20)30480-1 · Cited by 28 · see citing works
Measles outbreak in South Africa, 2003-2005.
McMorrow, M., Gebremedhin, G., den Heever, J. V., Kezaala, R., Harris, B. N., Nandy, R. K., Strebel, P. M., Jack, A., & Cairns, K. L. (2009) · PubMed · Cited by 28 · see citing works
Impaired Haemophilus influenzae Type b Transplacental Antibody Transmission and Declining Antibody Avidity through the First Year of Life Represent Potential Vulnerabilities for HIV-Exposed but -Uninfected Infants
Gaensbauer, J. T., Rakhola, J. T., Onyango‐Makumbi, C., Mubiru, M. C., Westcott, J., Krebs, N. F., Asturias, E. J., Fowler, M. G., McFarland, E. J., & Janoff, E. N. (2014) · Clinical and Vaccine Immunology · doi:10.1128/cvi.00356-14 · Cited by 26 · see citing works
Systematic Review of Measles and Rubella Serology Studies
Thompson, K. M., & Odahowski, C. L. (2015) · Risk Analysis · doi:10.1111/risa.12430 · Cited by 26 · see citing works
P. falciparum infection and maternofetal antibody transfer in malaria-endemic settings of varying transmission
McLean, A. R. D., Stanisic, D. I., McGready, R. M., Chotivanich, K., Clapham, C., Baiwog, F., Pimanpanarak, M., Siba, P., Müeller, I., King, C. L., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0186577 · Cited by 25 · see citing works
Maternal HIV infection associated with reduced transplacental transfer of measles antibodies and increased susceptibility to disease
Jallow, S., Cutland, C., Masbou, A. K., Adrian, P. V., & Madhi, S. A. (2017) · Journal of Clinical Virology · doi:10.1016/j.jcv.2017.07.009 · Cited by 24 · see citing works
Placental malaria and immunity to infant measles
Owens, S. (2006) · Archives of Disease in Childhood · doi:10.1136/adc.2005.085274 · Cited by 23 · see citing works
Reduced Placental Transfer of Antibodies Against a Wide Range of Microbial and Vaccine Antigens in HIV-Infected Women in Mozambique
Alonso, S., Vidal, M., Ruiz‐Olalla, G., González, R., Manaca, M. N., Jairoce, C., Vázquez-Santiago, M., Balcells, R., Valá, A., Rupérez, M., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.614246 · Cited by 22 · see citing works
Changes in Measles Serostatus Among HIV-Infected Zambian Children Initiating Antiretroviral Therapy Before and After the 2010 Measles Outbreak and Supplemental Immunization Activities
Rainwater‐Lovett, K., Nkamba, H., Mubiana‐Mbewe, M., Bolton‐Moore, C., & Moss, W. J. (2013) · The Journal of Infectious Diseases · doi:10.1093/infdis/jit404 · Cited by 21 · see citing works
Factors That Influence Infant Immunity and Vaccine Responses
Zimmermann, P., & Jones, C. E. (2021) · The Pediatric Infectious Disease Journal · doi:10.1097/inf.0000000000002773 · Cited by 18 · see citing works
Maternal Human Immunodeficiency Virus-Associated Hypergammaglobulinemia Reduces Transplacental Transfer of Immunoglobulin G to Plasmodium falciparum Antigens in Cameroonian Neonates
Babakhanyan, A., Ekali, G. L., Dent, A. E., Kazura, J. W., Nguasong, J. T., Fodjo, B. A. Y., Yuosembom, E. K., Esemu, L. F., Taylor, D. W., & Leke, R. G. F. (2016) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofw092 · Cited by 19 · see citing works
Effect of Placental Malaria and HIV Infection on the Antibody Responses toPlasmodium falciparumin Infants
Ned, R. M., Price, A. E., Crawford, S. B., Ayisi, J., van Eijk, A. M., Otieno, J. A., Nahlen, B. L., Steketee, R. W., Slutsker, L., Shi, Y. P., et al. (2008) · The Journal of Infectious Diseases · doi:10.1086/593066 · Cited by 19 · see citing works
Population-Level Risk Factors Related to Measles Case Fatality: A Conceptual Framework Based on Expert Consultation and Literature Review
Sbarra, A. N., Jit, M., Mosser, J. F., Ferrari, M. J., Cutts, F. T., Papania, M. J., Kretsinger, K., McCarthy, K. A., Thakkar, N., Gaythorpe, K. A. M., et al. (2023) · Vaccines · doi:10.3390/vaccines11081389 · Cited by 18 · see citing works
Self-citation
Placental Transfer of Respiratory Syncytial Virus Antibody Among HIV-Exposed, Uninfected Infants
Patel, S. M., Jallow, S., Boiditswe, S. C., Madhi, S. A., Feemster, K. A., Steenhoff, A. P., Arscott‐Mills, T., Muthoga, C. W., Ajibola, G., Shapiro, R., et al. (2019) · Journal of the Pediatric Infectious Diseases Society · doi:10.1093/jpids/piz056 · Cited by 18 · see citing works
Measles-specific Neutralizing Antibodies in Rural Mozambique: Seroprevalence and Presence in Breast Milk
Mandomando, I., Naniche, D., Pasetti, M. F., Vallès, X., Cuberos, L., Nhacolo, A., Kotloff, K. L., Martins, H., Levine, M. M., & Alonso, P. L. (2008) · American Journal of Tropical Medicine and Hygiene · doi:10.4269/ajtmh.2008.79.787 · Cited by 17 · see citing works
Vaccination of HIV-infected pregnant women: implications for protection of their young infants
Dangor, Z., Nunes, M. C., Kwatra, G., Lala, S. G., & Madhi, S. A. (2017) · Tropical Diseases Travel Medicine and Vaccines · doi:10.1186/s40794-016-0044-7 · Cited by 17 · see citing works
Seroprevalence of measles IgG among HIV-1-infected and uninfected Kenyan adults
Merkel, M. O., Ben-Youssef, L., Newman, L. P., Gitome, V., Gataguta, A., Lohman-Payne, B. L., Bosire, R. K., & Farquhar, C. (2013) · International Journal of Infectious Diseases · doi:10.1016/j.ijid.2013.10.018 · Cited by 16 · see citing works
Maternal Risk Factors Associated with Low Birth Weight Neonates: A Multi-Centre, Cross-Sectional Study in a Developing Country
O, I. K. N. B. (2015) · Journal of Neonatal Biology · doi:10.4172/2167-0897.1000190 · Cited by 16 · see citing works
Higher Transplacental Pathogen-Specific Antibody Transfer Among Pregnant Women Randomized to Triple Antiretroviral Treatment Versus Short Course Zidovudine
Bosire, R. K., Farquhar, C., Nduati, R. W., Broliden, K., Luchters, S. M. F., de Perre, P. V., de Vincenzi, I., Merkel, M. O., Wachuka, V., Mbori‐Ngacha, D., et al. (2017) · The Pediatric Infectious Disease Journal · doi:10.1097/inf.0000000000001749 · Cited by 16 · see citing works
HIV infection and placental malaria reduce maternal transfer of multiple antimalarial antibodies in Mozambican women
Alonso, S., Vidal, M., Ruiz‐Olalla, G., González, R., Jairoce, C., Manaca, M. N., Vázquez-Santiago, M., Balcells, R., Valá, A., Rupérez, M., et al. (2021) · Journal of Infection · doi:10.1016/j.jinf.2021.02.024 · Cited by 15 · see citing works
Assessment of the Epidemiology and Burden of Measles in Southern Mozambique
Mandomando, I., Naniche, D., Pasetti, M. F., Cuberos, L., Sanz, S., Vallès, X., Sigaúque, B., Macete, E., Nhalungo, D. A., Kotloff, K. L., et al. (2011) · American Journal of Tropical Medicine and Hygiene · doi:10.4269/ajtmh.2011.10-0517 · Cited by 13 · see citing works
Immunity to Measles in Pregnant Mothers and in Cord Blood of Their Infants: Impact of HIV Status and Mother’s Place of Birth
Choudhury, S. A., Hatcher, F. M., Berthaud, V., Ladson, G. M., Hills, E. R., & Humphrey, A. (2008) · Journal of the National Medical Association · doi:10.1016/s0027-9684(15)31545-5 · Cited by 13 · see citing works
The effects of maternal immunity and age structure on population immunity to measles
McKee, A., Ferrari, M. J., & Shea, K. (2015) · Theoretical Ecology · doi:10.1007/s12080-014-0250-8 · Cited by 12 · see citing works
Measles antibodies in cord blood in Portugal: Possible consequences for the recommended age of vaccination
Gonçalves, G., Nunes, C., Mesquita, J. R., Nascimento, M. S. J., & Frade, J. (2016) · Vaccine · doi:10.1016/j.vaccine.2016.04.007 · Cited by 11 · see citing works
Le passage placentaire des immunoglobulines
Éléfant, É. (2012) · Bulletin de l Académie Nationale de Médecine · doi:10.1016/s0001-4079(19)31686-3 · Cited by 11 · see citing works
Sex, Pregnancy and Measles
Brown, A. C., & Moss, W. J. (2009) · Springer eBooks · doi:10.1007/978-3-642-02155-8_11 · Cited by 10 · see citing works
Transplacental transfer of macromolecules: Proving the efficiency of placental transfer of maternal measles antibodies in mother: Infant pairs
Baba, U. A., Ashir, G., Mava, Y., Elechi, H., Saidu, G., & Kaleb, A. (2014) · Annals of Medical and Health Sciences Research · doi:10.4103/2141-9248.141975 · Cited by 9 · see citing works
Risk Factors for Measles in Young Infants in an Urban African Area With High Measles Vaccination Coverage
Bale, C., Garly, M., Martins, C. L., Nielsen, J. O., Whittle, H. C., & Aaby, P. (2011) · The Pediatric Infectious Disease Journal · doi:10.1097/inf.0b013e31821786a4 · Cited by 8 · see citing works
Prevalence of Placental Malaria and Effects on Birth Weight of Neonate of Mothers Who Had Antenatal Care in Maiduguri Metropolitan City, Nigeria
Ahmadu, B. U. (2014) · Journal of Advances in Medicine and Medical Research · doi:10.9734/bjmmr/2014/9023 · Cited by 8 · see citing works
The Role of Maternal HIV Envelope-Specific Antibodies and Mother-to-Child Transmission Risk
Douglas, A. O., Martinez, D. R., & Permar, S. R. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01091 · Cited by 8 · see citing works
Cotreatment of Congenital Measles with Vitamin A and Intravenous Immunoglobulin
Özsürekçi, Y., Kara, A., Bayhan, C., Öncel, E. K., Takçı, Ş., Yolbakan, S., Korkmaz, A., & Korukluoğlu, G. (2014) · Case Reports in Infectious Diseases · doi:10.1155/2014/234545 · Cited by 7 · see citing works
Tetanus Immunity in Neonates in a Developed Country
Prusa, A., Wiedermann, U., Kasper, D. C., Hayde, M., Helmer, H., Pollak, A. J., & Förster‐Waldl, E. (2011) · Neonatology · doi:10.1159/000320637 · Cited by 6 · see citing works
Measles Vaccines
Moss, W. J., & Strebel, P. M. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-79058-1.00038-4 · Cited by 6 · see citing works
Vaccination of human immunodeficiency virus–infected persons
Moss, W. J., Sutcliffe, C. G., & Halsey, N. A. (2013) · Elsevier eBooks · doi:10.1016/b978-1-4557-0090-5.00014-8 · Cited by 6 · see citing works
Maternal Immunization
Omer, S. B., & Jamieson, D. J. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-35761-6.00036-5 · Cited by 6 · see citing works
HLA antibody repertoire in infants suggests selectivity in transplacental crossing
Savulescu, D. M., Groome, M. J., Malfeld, S., Madhi, S. A., Koen, A. L., Jones, S., Duxbury, V., Scheuermaier, K. D., Rosa, D. D. A., & Suchard, M. S. (2020) · American Journal of Reproductive Immunology · doi:10.1111/aji.13264 · Cited by 5 · see citing works
Immune surveillance for six vaccinable pathogens using paired plasma and dried blood spots in HIV infected and uninfected children in Kinshasa
Rodríguez-Galet, A., Rubio-Garrido, M., Valadés-Alcaraz, A., Rodríguez-Domínguez, M., Galán, J. C., Ndarabu, A., Reina, G., & Holguín, Á. (2022) · Scientific Reports · doi:10.1038/s41598-022-12052-4 · Cited by 5 · see citing works
Impaired neutralizing activity by transplacental measles antibodies in infants born to HIV‐1‐infected mothers
Farouk, S. E., Navér, L., & Smedman, L. (2012) · Acta Paediatrica · doi:10.1111/j.1651-2227.2012.02793.x · Cited by 5 · see citing works
Impact of Maternal HIV Infection and Placental Malaria on the Transplacental Transfer of Influenza Antibodies in Mother–Infant Pairs in Malawi, 2013–2014
Ho, A. Y. W., Mapurisa, G. N., Madanitsa, M., Kalilani‐Phiri, L., Kamiza, S., Makanani, B., ter Kuile, F. O., Buys, A., Treurnicht, F. K., Everett, D., et al. (2019) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofz383 · Cited by 5 · see citing works
Tétanos et VIH : une association fortuite ?
Wateba, M. I., Diop, S. A., Nichols, S., Adjoh, S. K., Gbadamassi, G., Patassi, A., & Tidjani, O. (2008) · Cahiers d'études et de recherches francophones / Santé · doi:10.1684/san.2008.0114 · Cited by 5 · see citing works
Effect of Maternal HIV Infection on Measles Susceptibility During Early Infancy: Implications for Optimizing Protection of the Infant
Kruczek, A., Cutland, C., & Madhi, S. A. (2010) · HIV Therapy · doi:10.2217/hiv.10.31 · Cited by 4 · see citing works
Vaccination of human immunodeficiency virus-infected persons
Moss, W. J., & Halsey, N. A. (2008) · Elsevier eBooks · doi:10.1016/b978-1-4160-3611-1.50068-4 · Cited by 4 · see citing works
Pediatric Human Immunodeficiency Virus Infection
Weinberg, G. A., & Siberry, G. K. (2015) · Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases · doi:10.1016/b978-1-4557-4801-3.00129-6 · Cited by 4 · see citing works
Timing of HIV Seroreversion Among HIV-Exposed, Breastfed Infants in Malawi: Type of HIV Rapid Test Matters
Smith, E. R., Hudgens, M. G., Sheahan, A., Miller, W. C., Wheeler, S. B., Nelson, J. A. E., Dube, Q., & Rie, A. V. (2016) · Maternal and Child Health Journal · doi:10.1007/s10995-016-2152-4 · Cited by 3 · see citing works
Seroprevalence of transplacentally acquired measles antibodies in HIV-exposed versus HIV-unexposed infants at six months of age
Jain, S., Seth, A., Khare, S., & Chandra, J. (2017) · The Indian Journal of Medical Research · doi:10.4103/ijmr.ijmr_44_16 · Cited by 2 · see citing works
Measles: The road to eradication
Sato, A. I., & Chatterjee, A. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-85730-7.00063-1 · Cited by 2 · see citing works
Rural Kenya: Measles during Pregnancy and Early Infancy
Arya, S. C., & Agarwal, N. (2005) · The Journal of Infectious Diseases · doi:10.1086/498580 · Cited by 2 · see citing works
The effects of maternal haemoglobin as an indicator of maternal nutritional status on, maternal measles antibodies of mother-infant pairs at birth
Baba, U. A., Ashir, G., Mava, Y., Gimba, M., Abubakar, R., & Ambe, J. P. (2014) · African Health Sciences · doi:10.4314/ahs.v13i4.12 · Cited by 2 · see citing works
Birth weight outcome of babies whose mothers are infected with Human Immunodeficiency Virus and on antiretroviral therapy at University of Maiduguri Teaching Hospital, Nigeria
Ahmadu, B. U., Inuwa, U., Halima, U. I., Kyari, S. M., Jungudu, U., & Mshelbwala, B. S. (2013) · Greener Journal of Medical Sciences · doi:10.15580/gjms.2013.2.103112184 · Cited by 2 · see citing works
The Effects of Maternal Malaria and HIV‐1 Infection on the Effort to Eliminate Neonatal Tetanus
Moss, W. J., & Halsey, N. A. (2007) · The Journal of Infectious Diseases · doi:10.1086/519849 · Cited by 2 · see citing works

Passive measles immunity in a Nigerian tertiary health care facility: the influence of human immunodeficiency virus infection on measles antibody levels in mother-infant pairs at birth.
Baba, U. A., Mustapha, M. G., Ashir, G. M., Rabasa, A., Ibrahim, B., & Ibrahim, H. A. (2012) · PubMed
Maternal HIV infection associated with reduced transplacental transfer of measles antibodies and increased susceptibility to disease
Jallow, S., Cutland, C., Masbou, A. K., Adrian, P. V., & Madhi, S. A. (2017) · Journal of Clinical Virology · doi:10.1016/j.jcv.2017.07.009 · Cited by 24 · 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
Immunity to Measles in Pregnant Mothers and in Cord Blood of Their Infants: Impact of HIV Status and Mother’s Place of Birth
Choudhury, S. A., Hatcher, F. M., Berthaud, V., Ladson, G. M., Hills, E. R., & Humphrey, A. (2008) · Journal of the National Medical Association · doi:10.1016/s0027-9684(15)31545-5 · Cited by 13 · see citing works
Impaired neutralizing activity by transplacental measles antibodies in infants born to HIV‐1‐infected mothers
Farouk, S. E., Navér, L., & Smedman, L. (2012) · Acta Paediatrica · doi:10.1111/j.1651-2227.2012.02793.x · Cited by 5 · see citing works

Authors: Scott, S., Cumberland, P., Shulman, C. E., Cousens, S., Cohen, B. J., Brown, D. W. G., Bulmer, J. N., Dorman, E. K., Kawuondo, K., Marsh, K., & Cutts, F.
Affiliations: London School of Hygiene & Tropical Medicine (GB)
Institute of Child Health (IN)
Kenya Medical Research Institute (KE)
Health Protection Agency (GB)
Royal Victoria Infirmary (GB)
ORCID: Scott, Susana
Shulman, Caroline E.
Cousens, Simon
Brown, David W. G.
Bulmer, Judith N.
Marsh, Kevin
Cutts, Felicity
Venue: The Journal of Infectious Diseases
Publisher: Oxford University Press (OUP)
Published: 2005-06
Volume: 191
Issue: 11
Pages: 1854-1860
ISSN: 0022-1899 (ISSN-L)
1537-6613
DOI: 10.1086/429963
OpenAlex: W2096035536
Cited by: 117
References: 38
Citations by year: 2026: 1 · 2023: 5 · 2022: 3 · 2021: 3 · 2020: 3 · 2019: 6 · 2018: 4 · 2017: 12 · 2016: 6 · 2015: 10 · 2014: 7 · 2013: 9 · 2012: 6
FWCI: 5.70
Type: journal article
Language: en
Open access: bronze
doi.org
Locations: The Journal of Infectious Diseases (publishedVersion)
PubMed (publishedVersion)
UCL Discovery (University College London) (submittedVersion)
HighWire Press Open Archive (submittedVersion)
Newcastle University ePrints (Newcastle Univesity)
Topics: Health Sciences › Medicine › Epidemiology › Virology and Viral Diseases
Social Sciences › Health › Vaccine Coverage and Hesitancy
Health Sciences › Medicine › Infectious Diseases › HIV/AIDS Research and Interventions
Keywords: transplacental antibody transfer, HIV in pregnancy, placental malaria, cord serum, maternal serum, preterm birth, maternal age, rural Kenya
MeSH terms: Adolescent, Adult, Antibodies, Viral, Female, Fetal Blood, Humans, Immunity, Maternally-Acquired, Infant, Newborn, Kenya, Malaria, Measles, Placenta, Pregnancy, Pregnancy Complications, Infectious, Risk Factors, Rural Population, HIV Infections

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Neonatal measles immunity in rural Kenya: the influence of HIV and placental malaria infections on placental transfer of antibodies and levels of antibody in maternal and cord serum samples

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