Association between immunogenicity of a monovalent parenteral P2-VP8 subunit rotavirus vaccine and fecal shedding of rotavirus following Rotarix challenge during a randomized, double-blind, placebo-controlled trial
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Association between immunogenicity of a monovalent parenteral P2-VP8 subunit rotavirus vaccine and fecal shedding of rotavirus following Rotarix challenge during a randomized, double-blind, placebo-controlled trial
A correlate of protection for rotavirus (RV) has not been consistently identified. Shedding
of RV following an oral rotavirus vaccine (ORV) challenge has been investigated as a potential
model to assess protection of parenteral RV vaccines. We previously showed that shedding of a
challenge ORV dose was significantly reduced among recipients of a parenteral monovalent RV
subunit vaccine (P2-VP8-P[8]) compared to placebo recipients. This secondary data analysis assessed
the association between fecal shedding of RV, as determined by ELISA one week after receipt of a
Rotarix challenge dose at 18 weeks of age, and serum RV-specific antibody responses, one and six
months after vaccination with the third dose of the P2-VP8-P[8] vaccine or placebo. We did not find
any association between serum RV-specific immune responses measured one month post-P2-VP8-P[8]
vaccination and fecal shedding of RV post-challenge. At nine months of age, six months after the third
P2-VP8-P[8] or placebo injection and having received three doses of Rotarix, infants shedding RV
demonstrated higher immune responses than non-shedders, showing that RV shedding is reflective
of vaccine response following ORV. Further evaluation is needed in a larger sample before fecal
shedding of an ORV challenge can be used as a measure of field efficacy in RV vaccine trials.
Description:
SUPPLEMENTARY MATERIALS : TABLE S1: Baseline demographic and clinical factors between rotavirus shedders and non-shedders, as determined by ELISA, stratified by vaccination status: three injections of P2-VP8-P[8] vaccine (30 g and 60 g doses; n = 91) or placebo (n = 44); FIGURE S1: Schedule of events for infants.
DATA AVAILABILITY STATEMENT : The data presented in this study are available on request from the corresponding author. The data are not publicly available due to a clinical trial agreement with PATH Vaccine Solutions.