Effect of human rotavirus vaccine on severe diarrhea in African infants

被引:0
|
作者
Madhi, Shabir A. [1 ]
Cunliffe, Nigel A. [2 ]
Steele, Duncan [3 ]
Witte, Desiree [2 ,4 ]
Kirsten, Mari [5 ]
Louw, Cheryl [6 ,7 ]
Ngwira, Bagrey [4 ]
Victor, John C. [8 ]
Gillard, Paul H. [9 ]
Cheuvart, Brigitte B. [9 ]
Han, Htay H. [9 ]
Neuzil, Kathleen M. [8 ]
机构
[1] Univ Witwatersrand, Vaccine Preventable Dis, Johannesburg, South Africa
[2] Univ Liverpool, Div Med Microbiol, Liverpool, Merseyside, England
[3] WHO, Initiat Vaccine Res, Geneva, Switzerland
[4] Univ Malawi, Coll Med, Blantyre, Malawi
[5] Univ Pretoria, Dept Paediat Surg, Pretoria, South Africa
[6] Madibeng Ctr Res, Brits, South Africa
[7] Univ Limpopo, MRC, Diarrhoeal Pathogens Res Unit, Limpopo, South Africa
[8] PATH, Rotavirus Vaccine Program, Seattle, WA USA
[9] GlaxoSmithKline Biol, Rixensart, Belgium
基金
英国惠康基金;
关键词
EFFICACY; GASTROENTERITIS; PROTECTION; RIX4414; STRAINS; SAFETY; GENOTYPES; ANTIBODY; CHILDREN;
D O I
暂无
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background Rotavirus is the most common cause of severe gastroenteritis among young children worldwide. Data are needed to assess the efficacy of the rotavirus vaccine in African children. Methods We conducted a randomized, placebo-controlled, multicenter trial in South Africa (3166 infants; 64.1% of the total) and Malawi (1773 infants; 35.9% of the total) to evaluate the efficacy of a live, oral rotavirus vaccine in preventing severe rotavirus gastroenteritis. Healthy infants were randomly assigned in a 1: 1: 1 ratio to receive two doses of vaccine (in addition to one dose of placebo) or three doses of vaccine - the pooled vaccine group - or three doses of placebo at 6, 10, and 14 weeks of age. Episodes of gastroenteritis caused by wild-type rotavirus during the first year of life were assessed through active follow-up surveillance and were graded with the use of the Vesikari scale. Results A total of 4939 infants were enrolled and randomly assigned to one of the three groups; 1647 infants received two doses of the vaccine, 1651 infants received three doses of the vaccine, and 1641 received placebo. Of the 4417 infants included in the per-protocol efficacy analysis, severe rotavirus gastroenteritis occurred in 4.9% of the infants in the placebo group and in 1.9% of those in the pooled vaccine group (vaccine efficacy, 61.2%; 95% confidence interval, 44.0 to 73.2). Vaccine efficacy was lower in Malawi than in South Africa (49.4% vs. 76.9%); however, the number of episodes of severe rotavirus gastroenteritis that were prevented was greater in Malawi than in South Africa (6.7 vs. 4.2 cases prevented per 100 infants vaccinated per year). Efficacy against all-cause severe gastroenteritis was 30.2%. At least one serious adverse event was reported in 9.7% of the infants in the pooled vaccine group and in 11.5% of the infants in the placebo group. Conclusions Human rotavirus vaccine significantly reduced the incidence of severe rotavirus gastroenteritis among African infants during the first year of life.
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页码:108 / 114
页数:7
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