Rotavirus Vaccine Take in Infants Is Associated With Secretor Status
dc.contributor.author | Armah, G.E. | |
dc.contributor.author | Cortese, M.M. | |
dc.contributor.author | Dennis, F.E. | |
dc.contributor.author | Yu, Y. | |
dc.contributor.author | Morrow, A.L. | |
dc.contributor.author | McNeal, M.M. | |
dc.contributor.author | Lewis, K.D.C. | |
dc.contributor.author | Awuni, D.A. | |
dc.contributor.author | Armachie, J. | |
dc.contributor.author | Parashar, U.D. | |
dc.date.accessioned | 2019-05-21T11:12:34Z | |
dc.date.available | 2019-05-21T11:12:34Z | |
dc.date.issued | 2019-03 | |
dc.description.abstract | Rotaviruses bind to enterocytes in a genotype-specific manner via histo-blood group antigens (HBGAs), which are also detectable in saliva. We evaluated antirotavirus immunoglobulin A seroconversion (‘vaccine take”) among 166 Ghanaian infants after 2–3 doses of G1P[8] rotavirus vaccine during a vaccine trial, by HBGA status from saliva collected at age 4.1 years. Only secretor status was associated with seroconversion: 41% seroconversion for secretors vs 13% for nonsecretors; relative risk, 3.2 (95% confidence interval, 1.2–8.1; P = .016). Neither Lewis antigen nor salivary antigen blood type was associated with seroconversion. Likelihood of “take” for any particular rotavirus vaccine may differ across populations based on HBGAs. | en_US |
dc.identifier.other | https://doi.org/10.1093/infdis/jiy573 | |
dc.identifier.other | Volume 219, Issue 5,Pages 746–749 | |
dc.identifier.uri | http://ugspace.ug.edu.gh/handle/123456789/30136 | |
dc.language.iso | en | en_US |
dc.publisher | Journal of Infectious Diseases | en_US |
dc.subject | FUT2 | en_US |
dc.subject | Lewis antigen | en_US |
dc.subject | Rotavirus | en_US |
dc.subject | Secretor | en_US |
dc.subject | Vaccine | en_US |
dc.title | Rotavirus Vaccine Take in Infants Is Associated With Secretor Status | en_US |
dc.type | Article | en_US |
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