Development of a rotavirus vaccine: Clinical safety, immunogenicity, and efficacy of the pentavalent rotavirus vaccine, RotaTeq®

被引:91
作者
Ciarlet, Max [1 ]
Schoedel, Florian [1 ]
机构
[1] Merck Res Labs, Infect Dis & Vaccines Clin Res Dept, N Wales, PA 19454 USA
关键词
Rotavirus; Vaccine; Development; Gastroenteritis; Efficacy; Immunogenicity; PLACEBO-CONTROLLED TRIAL; GROUP-A ROTAVIRUSES; HEALTHY INFANTS; YOUNG-CHILDREN; UNITED-STATES; CONCOMITANT USE; STRAIN WC3; SEROTYPE-1; REASSORTANT; PROTECTIVE IMMUNITY; VENEZUELAN INFANTS;
D O I
10.1016/j.vaccine.2009.09.107
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Initial approaches for rotavirus vaccines were based on the classical "Jennerian" approach and utilized simian and bovine rotavirus strains, which provided cross-protection against human rotavirus strains but did not cause illness in infants and young children because of their species-specific tropism. The demonstrated efficacy of these vaccines was not consistent across studies. Thus, human-animal reassortants containing an animal rotavirus backbone with human rotavirus surface G and/or P proteins were developed, which demonstrated more consistent efficacy than that observed with the non-reassortant rotavirus strains. The pentavalent rotavirus vaccine, RotaTeq (R), contains 5 human-bovine reassortant rotaviruses consisting of a bovine (WC3) backbone with human rotavirus surface proteins representative of the most common G (G1, G2, G3, G4) or P (PIA[8]) types worldwide. The present review focuses on the development of the pentavalent rotavirus vaccine RotaTeq (R). Results of a large-scale Phase III clinical study showed that three doses of RotaTeq (R) were immunogenic, efficacious, and well tolerated with no increased clinical risk of intussusception. RotaTeq (R) was efficacious against rotavirus gastroenteritis of any severity (74%) and severe disease (98-100%), using a validated clinical scoring system. Reductions in rotavirus-associated hospitalizations and emergency department (ED) visits, for up to 2 years post-vaccination, were 95% in Europe, 97% in the United States, and 90% in the Latin American/Caribbean regions. RotaTeq (R) was recently shown to be up to 100% effective in routine use in the US in reducing hospitalizations and ED visits and 96% effective in reducing physician visits. Additional Studies in 8 different locations in the US have shown 85-95% reduction in rotavirus-associated hospitalizations and/or ED visits in the first 2-2.5 years of routine use. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:G72 / G81
页数:10
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