| Literature DB >> 6755247 |
W Szmuness, C E Stevens, E J Harley, E A Zang, H J Alter, P E Taylor, A DeVera, G T Chen, A Kellner.
Abstract
We evaluated the efficacy of hepatitis B vaccine (Heptavax-B) containing only the ad subtype in a randomized, placebo-controlled, double-blind trial among 865 staff members of 43 hemodialysis units in the United States. Surface antibody developed in 92.6 per cent of the subjects after two doses of vaccine and in 96 per cent after the six-month booster. The incidence of infections with hepatitis B virus (with or without hepatitis) was 9.9 per cent in placebo recipients and 2.2 per cent in vaccine recipients (P less than 0.01). The two cases of hepatitis B among vaccine recipients did not occur in subjects in whom antibody had developed. In 81 per cent of the hepatitis events, the virus was of the ay subtype. The indicence of ay virus was 8.2 per cent among placebo recipients and 1.2 per cent among vaccine recipients (P less than 0.005). We conclude that these data confirm the efficacy of the vaccine and demonstrate subtype cross-protection.Entities:
Mesh:
Substances:
Year: 1982 PMID: 6755247 DOI: 10.1056/NEJM198212093072403
Source DB: PubMed Journal: N Engl J Med ISSN: 0028-4793 Impact factor: 91.245