Mycobacterium tuberculosis-specific CD8+ T cells and their role in immunity

被引:134
作者
Woodworth, Joshua S. M.
Behar, Samuel M.
机构
[1] Brigham & Womens Hosp, Div Rheumatol Allergy & Immunol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
关键词
bacterial infection; T cells;
D O I
10.1615/CritRevImmunol.v26.i4.30
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
There are more cases of tuberculosis in the world today than at any other time in history. The global epidemic has generated intense interest into the immunological mechanisms that control infection. Although CD4(+) T cells play a critical role in host immunity to Mycobacterium tuberculosis, there is considerable interest in understanding the role of other T cell subsets in preventing disease development following infection. CD8(+) T cells are required for optimum host defense following M. tuberculosis infection, which has led to investigation into how this protective effect is mediated. A critical review of recent literature regarding the role of CD8(+) T cells in protective immunity to M. tuberculosis infection is now required to address the strengths and weaknesses of these studies. In this article, we evaluate the evidence that CD8(+) T cells are critical in immunity to M. tuberculosis infection. We discuss the specific mycobacterial proteins that are recognized by CD8(+) T cells elicited during infection. Finally, we examine the effector mechanisms of CD8(+) T cells generated during infection and synthesize recent studies to consider the protective roles that these T cells serve in vivo.
引用
收藏
页码:317 / 352
页数:36
相关论文
共 227 条
[1]  
Algood HMS, 2004, J IMMUNOL, V173, P3287
[2]   Poor correspondence between predicted and experimental binding of peptides to class I MHC molecules [J].
Andersen, MH ;
Tan, L ;
Sondergaard, I ;
Zeuthen, J ;
Elliott, T ;
Haurum, JS .
TISSUE ANTIGENS, 2000, 55 (06) :519-531
[3]  
ANDERSEN P, 1995, J IMMUNOL, V154, P3359
[4]   Assembly and export of MHC class I peptide ligands [J].
Antoniou, AN ;
Powis, SJ ;
Elliott, T .
CURRENT OPINION IN IMMUNOLOGY, 2003, 15 (01) :75-81
[5]   Detection of active tuberculosis infection by T cell responses to early-secreted antigenic target 6-kDa protein and culture filtrate protein 10 [J].
Arend, SM ;
Andersen, P ;
van Meijgaarden, KE ;
Skjot, RLV ;
Subronto, YW ;
van Dissel, JT ;
Ottenhoff, THM .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (05) :1850-1854
[6]   PEPTIDE CONTRIBUTES TO THE SPECIFICITY OF POSITIVE SELECTION OF CD8+ T-CELLS IN THE THYMUS [J].
ASHTONRICKARDT, PG ;
VANKAER, L ;
SCHUMACHER, TNM ;
PLOEGH, HL ;
TONEGAWA, S .
CELL, 1993, 73 (05) :1041-1049
[7]   Cutting edge: Rapid in vivo killing by memory CD8 T cells [J].
Barber, DL ;
Wherry, EJ ;
Ahmed, R .
JOURNAL OF IMMUNOLOGY, 2003, 171 (01) :27-31
[8]   Purified protein derivative-activated type 1 cytokine-producing CD4+ T lymphocytes in the lung:: A characteristic feature of active pulmonary and nonpulmonary tuberculosis [J].
Barry, SM ;
Lipman, MC ;
Bannister, B ;
Johnson, MA ;
Janossy, G .
JOURNAL OF INFECTIOUS DISEASES, 2003, 187 (02) :243-250
[9]  
Bean AGD, 1999, J IMMUNOL, V162, P3504
[10]   Susceptibility of mice deficient in CD1D or TAP1 to infection with Mycobacterium tuberculosis [J].
Behar, SM ;
Dascher, CC ;
Grusby, MJ ;
Wang, CR ;
Brenner, MB .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (12) :1973-1980