Safety and immunogenicity of live, attenuated human rotavirus vaccine 89-12

DI Bernstein, VE Smith, JR Sherwood, GM Schiff… - Vaccine, 1998 - Elsevier
DI Bernstein, VE Smith, JR Sherwood, GM Schiff, DS Sander, D DeFeudis, DR Spriggs…
Vaccine, 1998Elsevier
The safety and immunogenicity of an orally administered live human rotavirus vaccine
candidate (89-12), attenuated by 33 passages in monkey kidney cells, were evaluated in
placebo-controlled trials in adults, children and infants. This strain was selected because
natural infections with 89-12-like rotaviruses provided 100% protection over two years. The
initial evaluations in adults, seropositive children and nine infants indicated that the vaccine
was safe. Two doses of vaccine (105 pfu dose− 1) or placebo were then given to 42 infants …
The safety and immunogenicity of an orally administered live human rotavirus vaccine candidate (89-12), attenuated by 33 passages in monkey kidney cells, were evaluated in placebo-controlled trials in adults, children and infants. This strain was selected because natural infections with 89-12-like rotaviruses provided 100% protection over two years. The initial evaluations in adults, seropositive children and nine infants indicated that the vaccine was safe. Two doses of vaccine (105 p.f.u. dose−1) or placebo were then given to 42 infants, aged from 6 to 26 weeks. No significant difference in side effects was seen. Seroconversion was demonstrated in 19 of 20 previously uninfected vaccine recipients, but ≥4-fold rises in 89-12 neutralizing antibody titers were detected in only seven subjects. Intestinal IgA responses were detected in 15 subjects. This attenuated human rotavirus was safe and immunogenic and should be further evaluated as a vaccine candidate.
Elsevier