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dc.contributor.authorChurch, JA
dc.contributor.authorChasekwa, B
dc.contributor.authorRukobo, S
dc.contributor.authorGovha, M
dc.contributor.authorLee, B
dc.contributor.authorCarmolli, MP
dc.contributor.authorNtozini, R
dc.contributor.authorMutasa, K
dc.contributor.authorMcNeal, MM
dc.contributor.authorMajo, FD
dc.contributor.authorTavengwa, NV
dc.contributor.authorKirkpatrick, BD
dc.contributor.authorMoulton, LH
dc.contributor.authorHumphrey, JH
dc.contributor.authorPrendergast, AJ
dc.date.accessioned2020-06-04T09:18:13Z
dc.date.available2020-01-26
dc.date.available2020-06-04T09:18:13Z
dc.date.issued2020-03-17
dc.identifier.issn0264-410X
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/64641
dc.description.abstractBACKGROUND: Oral rotavirus vaccines (RVV) have poor immunogenicity in low-income countries, for reasons that remain unclear. This study identified the determinants of RVV immunogenicity among infants in rural Zimbabwe. METHODS: Anti-rotavirus IgA titres were measured among a sub-group of infants enrolled in the Sanitation Hygiene Infant Nutrition Efficacy (SHINE) trial (NCT01824940). SHINE was a cluster-randomized trial of improved infant and young child feeding, and improved water, sanitation and hygiene (WASH) in two rural Zimbabwean districts. Infants received RVV as part of the national immunisation programme. Among HIV-unexposed infants in the non-WASH trial arms, we evaluated associations between potential risk factors (vaccine schedule and dose, maternal and infant nutritional status, infant diarrhoea, and household environment) and RVV immunogenicity (seroconversion, seropositivity and geometric mean titres) using multivariable regression. RESULTS: Among 219 infants with seroconversion data, 43 (20%) successfully seroconverted and 176 (80%) failed to seroconvert to RVV. Seroconversion was positively associated with a higher length-for-age Z-score (LAZ) around the time of vaccination (adjusted RR 1.27 (95% CI 1.04, 1.55), P = 0.021), and negatively associated with concurrent OPV and RVV administration (adjusted RR 0.36 (0.19, 0.71), P = 0.003). Among 472 infants with post-vaccination titres, a higher LAZ score was associated with increased seropositivity (aRR 1.21 (95% CI 1.06, 1.38), P = 0.004), and higher birthweight was associated with increased IgA titres (0.45 (95%CI 0.18, 1.09) U/mL greater per 100 g gain in birthweight; P = 0.001). CONCLUSIONS: Infant ponderal and linear growth were positively associated with RVV immunogenicity, while concurrent administration of OPV was negatively associated with RVV immunogenicity. Together, these findings suggest that improving foetal growth and separating RVV and OPV administration are plausible approaches to increasing RVV immunogenicity.en_US
dc.format.extent2870 - 2878
dc.languageeng
dc.publisherElsevieren_US
dc.relation.ispartofVaccine
dc.rightsThis is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
dc.subjectAfricaen_US
dc.subjectImmunogenicityen_US
dc.subjectInfantsen_US
dc.subjectOral vaccineen_US
dc.subjectRotavirusen_US
dc.titlePredictors of oral rotavirus vaccine immunogenicity in rural Zimbabwean infants.en_US
dc.typeArticleen_US
dc.rights.holder© 2020 The Authors. Published by Elsevier Ltd.
dc.identifier.doi10.1016/j.vaccine.2020.01.097
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/32088018en_US
pubs.issue13en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.publisher-urlhttps://doi.org/10.1016/j.vaccine.2020.01.097
pubs.volume38en_US
dcterms.dateAccepted2020-01-26
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US
qmul.funderThe impact of the intestinal environment on the immunogenicity of oral vaccines in Zimbabwean infants::Wellcome Trusten_US


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