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Clinical Trial
. 1993 Mar;82(3):223-7.
doi: 10.1111/j.1651-2227.1993.tb12646.x.

Take of rhesus-human reassortant tetravalent rotavirus vaccine in breast-fed infants

Affiliations
Clinical Trial

Take of rhesus-human reassortant tetravalent rotavirus vaccine in breast-fed infants

M Ceyhan et al. Acta Paediatr. 1993 Mar.

Abstract

Rhesus-human reassortant tetravalent rotavirus vaccine at a titer of 4 x 10(4) plaque forming units was evaluated for immunogenicity in 194 6-8-week-old breast-fed Turkish infants. The vaccine was administered orally as a single dose following either a meal of breast milk or 30 ml of sodium bicarbonate-buffered soy milk formula. Four-fold or greater responses in rotavirus IgA ELISA antibody were detected in 62% and 65% of the infants in the two groups, respectively (p = 0.62). In a smaller comparison group of non-breast-fed infants, an IgA response was detected in 7 of 11 (64%) cases. In all vaccinees, a serological response was detected in 72% of the initially seronegative and 47% of the initially seropositive infants (p = 0.001). We conclude that the take of rhesus-human reassortant tetravalent rotavirus vaccine in breast-fed infants is not compromised by breast feeding before vaccination. However, a higher titered preparation of the same vaccine may be required to improve overall immunogenicity in young infants, particularly in those with pre-vaccination rotavirus antibody.

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