Efficacy and immunogenicity of two or three dose rotavirus-vaccine regimen in South African children over two consecutive rotavirus-seasons: A randomized, double-blind, placebo-controlled trial

被引:87
作者
Madhi, S. A. [1 ,2 ]
Kirsten, M. [3 ]
Louw, C. [4 ]
Bos, P. [5 ]
Aspinall, S. [6 ]
Bouckenooghe, A. [7 ]
Neuzil, K. M. [8 ]
Steele, A. D. [8 ]
机构
[1] Natl Inst Communicable Dis, ZA-2131 Johannesburg, South Africa
[2] Univ Witwatersrand, Dept Sci & Technol, Natl Res Fdn Vaccine Preventable Dis, Johannesburg, South Africa
[3] Univ Pretoria, Dept Paediat Surg, ZA-0002 Pretoria, South Africa
[4] Madibeng Ctr Res, Brits, South Africa
[5] Univ Limpopo, MRC Diarrhoeal Pathogens Res Unit, Sovenga, South Africa
[6] Rota Consortium, Synexus Clin Res S Africa, Pretoria, South Africa
[7] Sanofi Pasteur, Singapore, Singapore
[8] PATH, Rotavirus Vaccine Program, Seattle, WA USA
关键词
Rotavirus; Diarrhea; Vaccine efficacy; Africa; GUINEA-BISSAU; WEST-AFRICA; GASTROENTERITIS; DIARRHEA; INFANTS; SAFETY; EPIDEMIOLOGY; DISEASE; SURVEILLANCE; COMMUNITY;
D O I
10.1016/j.vaccine.2011.08.080
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Human rotavirus vaccine (HRV; i.e.. Rotarix) reduced the incidence of severe rotavirus gastroenteritis (RVGE) by 77% (95% Confidence interval: 56-88%) during the first year of life in South Africa. Persistence of HRV-derived protection against RVGE during subsequent rotavirus seasons, although evident in industrialized settings, remains to be established in African settings. This study reports on the efficacy of HRV against severe RVGE over two consecutive rotavirus seasons in South African children. Methods: A prospective, double-blind, placebo controlled multi-centered trial in South Africa and Malawi randomly assigned infants in a 1:1:1 ratio to receive either two (10 and 14 weeks; HRV_2D) or three (6, 10 and 14 weeks; HRV_3D) doses of HRV or placebo. The primary analysis involved pooling of HRV_2D and HRV_3D arms. Episodes of gastroenteritis caused by wild-type rotavirus were identified through active follow-up surveillance and graded by the Vesikari scale. Results: 1339 infants (447 in the HRV_2D group, 447 in the HRV_3D group and 445 in the placebo group) were enrolled in Year 2 of the study, including 1035 (77.3%) who were followed up over two consecutive rotavirus seasons (i.e., Cohort 2 subjects). Rotarix was associated with ongoing protection against severe RVGE, preventing 2.5 episodes per 100 vaccinated children over two consecutive rotavirus seasons; vaccine efficacy: 59% (95% Confidence interval: 1-83%). An exploratory analysis indicated better immunogenicity (among Cohort 1 subjects) and a higher point-efficacy estimate over two seasons in the HRV_3D compared to HRV_2D arms of the study in Cohort 2 subjects. Conclusion: Rotarix is associated with significant reductions in severe gastroenteritis episodes through 2 years of life among South African children. Further research is needed to determine the optimal dosing schedule of Rotarix in providing long-term protection against rotavirus illness in African children. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:A44 / A51
页数:8
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