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Assays for the Specific Growth Rate and Cell-binding Ability of Rotavirus
Published on: January 28, 2019
Immunogenicity of tetravalent rhesus rotavirus vaccine administered with buffer and oral polio vaccine
D J Ing1, R I Glass, P A Woods
1Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.
Insights
Adding an antacid buffer significantly improved the immune response to the rhesus rotavirus vaccine (RRV-TV) in infants. The vaccine did not interfere with the oral polio vaccine response.
Area of Science:
- Pediatrics
- Immunology
- Vaccinology
Background:
- Rotavirus is a leading cause of severe diarrheal disease in infants globally.
- The tetravalent rhesus rotavirus vaccine (RRV-TV) was investigated for its efficacy and safety.
- Understanding optimal vaccine administration is crucial for public health.
Purpose of the Study:
- To determine the immunogenicity of RRV-TV with different antacid buffer regimens.
- To assess potential interference between RRV-TV and oral polio vaccine (OPV).
Main Methods:
- A randomized clinical trial involving 174 infants aged 6 to 16 weeks.
- Comparison of RRV-TV immunogenicity with no buffer, small-volume (2.5-mL) buffer, and large-volume (30-mL) buffer.
- Evaluation of antibody titers for rotavirus and poliovirus serotypes.
Main Results:
- RRV-TV immunogenicity, measured by a fourfold antibody titer rise, was significantly higher with both small- (45%) and large-volume (49%) antacid buffers compared to no buffer (23%).
- Co-administration of RRV-TV with OPV did not significantly impede the immune response to poliovirus serotypes 1, 2, or 3.
- Fourfold antibody titer rises for poliovirus serotypes 1, 2, and 3 were 29%, 87%, and 24%, respectively.
Conclusions:
- Antacid buffering enhances the immunogenicity of the tetravalent rhesus rotavirus vaccine in infants.
- RRV-TV can be safely administered with oral polio vaccine without compromising OPV immune responses.
Abstract:
Between January and November 1989, we studied 174 infants aged 6 to 16 weeks in a randomized clinical trial to (1) determine the immunogenicity of a single dose of tetravalent rhesus rotavirus vaccine (RRV-TV) when administered with three different buffer regimens: no antacid buffer and small-volume (2.5-mL) and large-volume (30-mL) antacid buffer; and (2) examine the potential interference of RRV-TV on the immune response to oral polio vaccine. Immunogenicity of RRV-TV, measured as a fourfold rise in antibody titers to rotavirus, was similar in the groups receiving small- and large-dose buffer (45% and 49%, respectively) and significantly less in the group that received RRV-TV alone (23%). Administration of RRV-TV with oral polio vaccine did not significantly interfere with the neutralization response of oral polio vaccine poliovirus serotypes 1, 2, or 3, and overall, 29%, 87%, and 24% of the infants had a fourfold rise in titer to each serotype, respectively.
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