Future Vaccination Strategies against Tuberculosis: Thinking outside the Box

被引:152
作者
Kaufmann, Stefan H. E. [1 ]
机构
[1] Max Planck Inst Infect Biol, Dept Immunol, D-10117 Berlin, Germany
基金
比尔及梅琳达.盖茨基金会;
关键词
T-CELL RESPONSES; MYCOBACTERIUM-BOVIS BCG; CALMETTE-GUERIN VACCINE; CHRONIC VIRAL-INFECTION; HEPARIN-BINDING HEMAGGLUTININ; IMMUNE-RESPONSES; EXTRAPULMONARY DISSEMINATION; ANTIGEN PRESENTATION; DEFENSE-MECHANISM; INTERFERON-GAMMA;
D O I
10.1016/j.immuni.2010.09.015
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
With almost a dozen vaccine candidates in clinical trials, tuberculosis (TB) research and development is finally reaping the first fruits of its labors Vaccine candidates in clinical trials may prevent TB disease reactivation by efficiently containing the pathogen Mycobacterium tuberculosis (Mtb) Future research should target vaccines that achieve sterile eradication of Mtb or even prevent stable infection These are ambitious goals that can be reached only by highly cooperative engagement of basic immunologists, vaccinologists, and clinical researchers or in other words, by translation from basic immunology to vaccine research and development, as well as reverse translation of insights from clinical trials back to hypothesis-driven research in the basic laboratory Here, we review current and future strategies toward the rational design of novel vaccines against TB, as well as the progress made thus far, and the hurdles that need to be overcome in the near and distant future
引用
收藏
页码:567 / 577
页数:11
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