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2型登革热病毒疫苗:士兵中的反应原性和免疫原性

Dengue virus type 2 vaccine: reactogenicity and immunogenicity in soldiers.

作者信息

Bancroft W H, Scott R M, Eckels K H, Hoke C H, Simms T E, Jesrani K D, Summers P L, Dubois D R, Tsoulos D, Russell P K

出版信息

J Infect Dis. 1984 Jun;149(6):1005-10. doi: 10.1093/infdis/149.6.1005.

Abstract

A live dengue virus type 2 (dengue-2) vaccine (PR-159/S-1) was tested for reactogenicity and immunogenicity in a placebo-controlled, double-blind clinical trial involving 98 soldiers. Seroconversion rates based on the development of neutralizing antibody to dengue-2 were 90% in 70 recipients with immunity to yellow fever and 61% in 28 vaccinees without such immunity (P less than .01). Peak titers of neutralizing antibody were three times higher in recipients with antibody to yellow fever virus and persisted in most for at least 18 months. Individuals seroconverting to the vaccine virus more frequently experienced systemic symptoms than those who received placebo (P less than .02). Future users of this dengue-2 vaccine may wish to employ immunization schedules that include preliminary immunization against yellow fever and must be prepared to accept mild vaccine-related symptoms in some recipients.

摘要

一种2型登革热活疫苗(PR - 159/S - 1)在一项涉及98名士兵的安慰剂对照双盲临床试验中进行了反应原性和免疫原性测试。基于对登革热2型中和抗体产生情况的血清转化率,在70名对黄热病有免疫力的接受者中为90%,在28名无此类免疫力的疫苗接种者中为61%(P小于0.01)。有黄热病病毒抗体的接受者中,中和抗体的峰值滴度高出三倍,且大多数人的抗体至少持续18个月。血清转化为疫苗病毒的个体比接受安慰剂的个体更频繁地出现全身症状(P小于0.02)。这种2型登革热疫苗的未来使用者可能希望采用包括针对黄热病进行初步免疫的免疫接种方案,并且必须准备好接受部分接受者出现的与疫苗相关的轻微症状。

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