New 30-valent M protein-based vaccine evokes cross-opsonic antibodies against non-vaccine serotypes of group A streptococci

被引:202
作者
Dale, James B. [1 ,2 ,3 ]
Penfound, Thomas A. [1 ,3 ]
Chiang, Edna Y. [1 ,3 ]
Walton, William J. [1 ]
机构
[1] Univ Tennessee, Hlth Sci Ctr, Dept Med, Memphis, TN 38163 USA
[2] Univ Tennessee, Hlth Sci Ctr, Dept Microbiol Immunol & Biochem, Memphis, TN 38163 USA
[3] Dept Vet Affairs Med Ctr, Memphis, TN 38163 USA
基金
美国国家卫生研究院;
关键词
Group A streptococci; Vaccine; M protein; UNITED-STATES; IMMUNOGENICITY; SURVEILLANCE; SAFETY;
D O I
10.1016/j.vaccine.2011.09.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Our previous studies have shown that recombinant multivalent vaccines containing amino-terminal M protein fragments from as many as 26 different serotypes of group A streptococci (GAS) evoked opsonic antibodies in animals and humans. In the present study, we constructed a new 30-valent vaccine containing M protein peptides from GAS serotypes prevalent in North America and Europe. The vaccine was immunogenic in rabbits and evoked bactericidal antibodies against all 30 vaccine serotypes of GAS. In addition, the vaccine antisera also contained significant levels of bactericidal antibodies against 24 of 40 non-vaccine serotypes of GAS. These results indicate that the potential efficacy of the new multivalent vaccine may be greater than predicted based on the "type-specific" M peptides represented. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:8175 / 8178
页数:4
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