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dc.contributor.authorRongsen-Chandola, Temsunaro
dc.contributor.authorStrand, Tor
dc.contributor.authorGoyal, Nidhi
dc.contributor.authorFlem, Elmira
dc.contributor.authorSingh Rathore, Sudeep
dc.contributor.authorArya, Alok
dc.contributor.authorWinje, Brita Askeland
dc.contributor.authorLazarus, Robin
dc.contributor.authorShanmugasundaram, Elango
dc.contributor.authorBabji, Sudhir
dc.contributor.authorSommerfelt, Halvor
dc.contributor.authorVainio, M Kirsti
dc.contributor.authorKang, Gagandeep
dc.contributor.authorBhandari, Nita
dc.date.accessioned2015-03-04T10:23:03Z
dc.date.accessioned2015-07-02T08:20:55Z
dc.date.available2015-03-04T10:23:03Z
dc.date.available2015-07-02T08:20:55Z
dc.date.issued2014
dc.identifier.citationVaccine 2014, 32:A134-A139
dc.identifier.issn0264-410X
dc.identifier.urihttp://hdl.handle.net/11250/286322
dc.description-
dc.description.abstractAbstract: Interference from transplacental and breast milk antibodies may impede the performance of oral live vaccines. The effect of breastfeeding on the immunogenicity of Rotarix®, a two-dose oral monovalent rotavirus vaccine, was examined in a community-based trial in New Delhi, India. Four hundred mother–infant pairs were randomized into two equal groups. Infants were aged 6–7 weeks at enrollment. Mothers were encouraged to either breastfeed or to withhold breastfeeding during the 30 min prior to and after each vaccine dose was administered. We collected blood specimens from infants at enrollment and 4 weeks after the second vaccine dose. Blood and breast milk specimens were obtained from mothers at baseline and breast milk specimens were collected at the time of the second vaccine dose. Seroconversion was defined as infant serum anti-VP6 IgA antibody level of ≥20 IU/mL 4 weeks after the second vaccine dose and a ≥4-fold rise from baseline. There was no difference in the proportion who seroconverted between the two groups (26% vs 27%; p = 0.92). The levels of infant serum IgA, maternal serum and breast milk IgA and IgG anti-rotavirus antibodies predicted the anti-rotavirus IgA level in infants at end-study and explained approximately 10% of the variability of the immune response (r2 = 0.10, p < 0.001). In this population, the immune response to Rotarix® was not enhanced by withholding breastfeeding around the time of vaccination. Maternal anti-rotavirus antibodies explained little of the variability in the immune response to the vaccine. Factors other than maternal anti-rotavirus antibodies probably explain why infants in low-and middle-income settings respond poorly to live oral rotavirus vaccines.
dc.language.isoeng
dc.titleEffect of withholding breastfeeding on the immune response to a live oral rotavirus vaccine in North Indian infants
dc.typeJournal article
dc.date.updated2015-03-04T10:23:02Z
dc.subject.nsiVDP::Medisinske fag: 700::Helsefag: 800::Forebyggende medisin: 804
dc.subject.nsiVDP::Midical sciences: 700::Health sciences: 800::Preventive medicine: 804
dc.subject.nsiVDP::Medisinske fag: 700::Helsefag: 800::Helsetjeneste- og helseadministrasjonsforskning: 806
dc.subject.nsiVDP::Midical sciences: 700::Health sciences: 800::Health service and health administration research: 806
dc.subject.nsiVDP::Medisinske fag: 700::Basale medisinske, odontologiske og veterinærmedisinske fag: 710::Medisinsk immunologi: 716
dc.subject.nsiVDP::Midical sciences: 700::Basic medical, dental and veterinary sciences: 710::Medical immunology: 716
dc.subject.nsiVDP::Medisinske fag: 700::Helsefag: 800::Samfunnsmedisin, sosialmedisin: 801
dc.subject.nsiVDP::Midical sciences: 700::Health sciences: 800::Community medicine, social medicine: 801
dc.identifier.doi10.1016/j.vaccine.2014.04.078
dc.identifier.cristin1152461
dc.relation.projectNorges forskningsråd: 223269


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