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乙肝疫苗(Heptavax B)疗效的对照临床试验:最终报告

A controlled clinical trial of the efficacy of the hepatitis B vaccine (Heptavax B): a final report.

作者信息

Szmuness W, Stevens C E, Zang E A, Harley E J, Kellner A

出版信息

Hepatology. 1981 Sep-Oct;1(5):377-85. doi: 10.1002/hep.1840010502.

Abstract

A controlled, randomized, double-blind trial in 1,083 homosexual men from New York confirmed that a highly purified, formalin-inactivated vaccine against hepatitis B prepared from HBsAg positive plasma, is safe immunogenic, and highly efficacious. Over 95% of vaccinated subjects developed antibody against the surface antigen. Vaccine-induced antibody persisted for the entire 24-month follow-up period. The attack rate of all hepatitis B virus infections (excluding conversions of anti-HBc alone) was 3.2% in vaccine recipients compared with 25.6% in placebo recipients (p less than 0.0001). In those who received all three doses of vaccine, of 40 micrograms each, the protective efficacy rate was close to 100%. The vaccine protects against acute hepatitis B, asymptomatic infection, and chronic antigenemia. There is reason to assume that the vaccine is also partially effective when given postexposure.

摘要

一项针对1083名来自纽约的同性恋男性的对照、随机、双盲试验证实,一种由乙肝表面抗原(HBsAg)阳性血浆制备的高度纯化、福尔马林灭活的乙肝疫苗是安全、具有免疫原性且高度有效的。超过95%的接种者产生了针对表面抗原的抗体。疫苗诱导的抗体在整个24个月的随访期内持续存在。疫苗接种者中所有乙肝病毒感染(不包括仅抗-HBc转换)的发病率为3.2%,而安慰剂接种者为25.6%(p小于0.0001)。在接受了每剂40微克的全部三剂疫苗的人群中,保护有效率接近100%。该疫苗可预防急性乙肝、无症状感染和慢性抗原血症。有理由认为,该疫苗在暴露后接种时也有部分效果。

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