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A controlled field trial of the typhoid component of polyvalent enteric vaccine (NIISI polyvaccine)

机译:多价肠溶疫苗(NIISI多疫苗)的伤寒成分的对照实地试验

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摘要

At the request of the Ministry of Health of the USSR, a controlled field trial of a polyvaccine containing typhoid, paratyphoid and dysentery antigens and a purified tetanus toxoid was undertaken in 1958. The main object of this trial, which was carried out over a 10-month period simultaneously in four localities, was to determine the efficacy of the typhoid component of the polyvaccine.The study population comprised over 90 000 individuals of 16-60 years of age. These were divided into two approximately equal groups, one of which received an injection of the polyvaccine under test and the other an injection of a preparation containing only the purified tetanus toxoid.The difference between the incidence of typhoid fever in the test group and that in the control group during the study period was statistically significant, and it was therefore concluded that a single injection of the polyvaccine afforded some protection against typhoid.
机译:应苏联卫生部的要求,于1958年对含有伤寒,副伤寒和痢疾抗原以及纯化的破伤风类毒素的多疫苗进行了对照试验。该试验的主要目的是进行10多次试验。在四个地方同时进行了一个月的研究,以确定多疫苗中伤寒成分的功效。研究人群包括9万多名16-60岁的个体。将它们分为两组,两组分别相等,其中一组接受测试的多疫苗疫苗注射,另一组接受仅包含纯化的破伤风类毒素的制剂注射。在研究期间,对照组具有统计学意义,因此得出结论,单次注射多疫苗可提供一定程度的针对伤寒的保护作用。

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