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伤寒Vi疫苗:一种反应原性较低的疫苗。

Typhoid Vi: a less reactogenic vaccine.

作者信息

Cumberland N S, St Clair Roberts J, Arnold W S, Patel R K, Bowker C H

机构信息

Queen Elizabeth Military Hospital, London, UK.

出版信息

J Int Med Res. 1992 Jun;20(3):247-53. doi: 10.1177/030006059202000306.

DOI:10.1177/030006059202000306
PMID:1397669
Abstract

A typhoid vaccine derived from the purified Vi capsular polysaccharide (CPS) antigen of Salmonella typhi was compared with a heat-killed whole-cell typhoid vaccine in 637 healthy male volunteers. The individuals were placed in three groups: group 1 received two doses of heat-killed whole-cell typhoid vaccine, at an interval of 28 days; group 2 received a single dose of typhoid Vi CPS vaccine followed after 28 days by water for injection; and group 3 received water for injection on the first occasion and a single dose of typhoid Vi CPS vaccine 28 days later. Local and systemic adverse reactions were recorded for 5 days following each injection. Subjects receiving the typhoid Vi CPS vaccine complained of fewer local adverse reactions on each of the first 3 days following immunization: on day 1, 18.6% of subjects given typhoid Vi CPS vaccine reported local reactions compared with 59.7% of those receiving heat-killed whole-cell vaccine (P less than 0.001). The percentage of subjects receiving the heat-killed whole-cell vaccine who complained of systemic reactions was more than twice that of subjects receiving the Vi CPS vaccine (7.9% and 3.4%, respectively, on day 1; P less than 0.01).

摘要

在637名健康男性志愿者中,对一种源自伤寒沙门氏菌纯化Vi荚膜多糖(CPS)抗原的伤寒疫苗与一种热灭活全细胞伤寒疫苗进行了比较。这些个体被分为三组:第1组间隔28天接种两剂热灭活全细胞伤寒疫苗;第2组接种一剂伤寒Vi CPS疫苗,28天后接种注射用水;第3组首次接种注射用水,28天后接种一剂伤寒Vi CPS疫苗。每次注射后记录5天的局部和全身不良反应。接种伤寒Vi CPS疫苗的受试者在免疫后的前3天中,每天抱怨的局部不良反应较少:第1天,接种伤寒Vi CPS疫苗的受试者中有18.6%报告有局部反应,而接种热灭活全细胞疫苗的受试者中有59.7%报告有局部反应(P<0.001)。抱怨有全身反应的接种热灭活全细胞疫苗的受试者比例是接种Vi CPS疫苗的受试者的两倍多(第1天分别为7.9%和3.4%;P<0.01)。

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Can J Infect Dis. 1995 Sep;6(5):231. doi: 10.1155/1995/919582.
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A cost-effectiveness analysis of typhoid fever vaccines in US military personnel.美国军事人员伤寒疫苗的成本效益分析。
Pharmacoeconomics. 1996 Nov;10(5):475-83. doi: 10.2165/00019053-199610050-00005.