Increased vaccine efficacy against tuberculosis of recombinant Mycobacterium bovis bacille Calmette-Guerin mutants that secrete listeriolysin

被引:430
作者
Grode, L
Seiler, P
Baumann, S
Hess, J
Brinkmann, V
Eddine, AN
Mann, P
Goosmann, C
Bandermann, S
Smith, D
Bancroft, GJ
Reyrat, JM
van Soolingen, D
Raupach, B
Kaufmann, SHE
机构
[1] Max Planck Inst Infect Biol, Dept Immunol, D-10117 Berlin, Germany
[2] London Sch Hyg & Trop Med, Immunol Unit, Dept Infect & Trop Dis, London WC1, England
[3] INSERM, Fac Med Necker, Paris, France
[4] Natl Inst Publ Hlth & Environm, Natl Mycobacteria Reference Lab, NL-3720 BA Bilthoven, Netherlands
关键词
D O I
10.1172/JCI24617
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The tuberculosis vaccine Mycobacterium bovis bacille Calmette-Guerin (BCG) was equipped with the membrane-perforating listeriolysin (Hly) of Listeria monocytogenes, which was shown to improve protection against Mycobacterium tuberculosis. Following aerosol challenge, the Hly-secreting recombinant BCG (hly(+) rBCG) vaccine was shown to protect significantly better against aerosol infection with M. tuberculosis than did the parental BCG strain. The isogenic, urease C-deficient hly(+) rBCG (Delta ureC hly(+) rBCG) vaccine, providing an intraphagosomal pH closer to the acidic pH optimum for Hly activity, exhibited still higher vaccine efficacy than parental BCG. Delta ureC hly(+) rBCG also induced profound protection against a member of the M. tuberculosis Beijing/W genotype family while parental BCG failed to do so consistently. Hly not only promoted antigen translocation into the cytoplasm but also apoptosis of infected macrophages. We concluded that superior vaccine efficacy of Delta ureC hly(+) rBCG as compared with parental BCG is primarily based on improved cross-priming, which causes enhanced T cell-mediated immunity.
引用
收藏
页码:2472 / 2479
页数:8
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