Next generation:: Tuberculosis vaccines that elicit protective CD8+ T cells

被引:42
作者
Behar, Samuel M.
Woodworth, Joshua S. M.
Wu, Ying
机构
[1] Brigham & Womens Hosp, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Div Rheumatol Allergy & Immunol, Boston, MA 02115 USA
关键词
animal models; bacterial infection; BCG; CD4; CD8; microbial immunity; Mycobarterium tuberculosis; T cell; vaccine;
D O I
10.1586/14760584.6.3.441
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tuberculosis continues to cause considerable human morbidity and mortality worldwide, particularly in people coinfected with HIV. The emergence of multidrug resistance makes the medical treatment of tuberculosis even more difficult. Thus, the development of a tuberculosis vaccine is a global health priority. Here we review the data concerning the role of CD8(+) T cells in immunity to tuberculosis and consider how CD8(+) T cells can be elicited by vaccination. Many immunization strategies have the potential to elicit CD8+ T cells and we critically review the data supporting a role for vaccine-induced CD8(+) T cells in protective immunity. The synergy between CD4(+) and CD8(+) T cells suggests that a vaccine that elicits both T-cell subsets has the best chance at preventing tuberculosis.
引用
收藏
页码:441 / 456
页数:16
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