Immunogenicity of a 26-valent group A streptococcal vaccine

被引:196
作者
Hu, MC
Walls, MA
Stroop, SD
Reddish, MA
Beall, B
Dale, JB
机构
[1] Univ Tennessee, Dept Vet Affairs Med Ctr 11A, Memphis, TN 38104 USA
[2] ID Biomed Corp, Bothell, WA USA
[3] Ctr Dis Control & Prevent, Resp Dis Branch, Atlanta, GA USA
[4] Univ Tennessee, Dept Med, Memphis, TN 38104 USA
关键词
D O I
10.1128/IAI.70.4.2171-2177.2002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A multivalent vaccine containing amino-terminal M protein fragments from 26 different serotypes of group A streptococci was constructed by recombinant techniques. The vaccine consisted of four different recombinant proteins that were formulated with alum to contain 400 mug of protein per dose. Rabbits were immunized via the intramuscular route at 0, 4, and 16 weeks. Immune sera were assayed for the presence of type-specific antibodies against the individual recombinant M peptides by enzyme-linked immunosorbent assay and for opsonic antibodies by in vitro opsonization tests and indirect bactericidal tests. The 26-valent vaccine was highly immunogenic and elicited fourfold or greater increases in antibody levels against 25 of the 26 serotypes represented in the vaccine. The immune sera were broadly opsonic and were bactericidal against the majority of the 26 different serotypes. Importantly, none of the immune sera cross-reacted with human tissues. Our results indicate that type-specific, protective M protein epitopes can be incorporated into complex, multivalent vaccines designed to elicit broadly protective opsonic antibodies in the absence of tissue-cross-reactive antibodies.
引用
收藏
页码:2171 / 2177
页数:7
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