Immunity against mycobacteria

被引:13
作者
Mason, CM [1 ]
Ali, J [1 ]
机构
[1] Louisiana State Univ, Hlth Sci Ctr, Div Pulm Crit Care Med, New Orleans, LA 70112 USA
关键词
mycobacteria; immunity; cytokines; granuloma;
D O I
10.1055/s-2004-822305
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
mycobacterium tuberculosis is the most prevalent infectious pathogen in the world, largely due to its unique interactions with the human immune system. Even in a normal host, a frequent outcome of infection with M. tuberculosis is failure to completely eradicate the organisms, despite the development of cell-mediated immunity. Viable organisms persist in a state in which they do not progressively replicate, leading to latent infection, which carries a risk of breakdown into active (reactivation) tuberculosis at some point later in life. Key features of the immune response against mycobacteria are reviewed here, and potential mechanisms by which the organisms may subvert these host defenses are discussed. Despite the multicellular nature of the host response to infecting mycobacteria, the organisms cannot be eradicated and contribute to the ongoing worldwide epidemic with tuberculosis.
引用
收藏
页码:53 / 61
页数:9
相关论文
共 67 条
[41]   GLOBAL EPIDEMIOLOGY OF TUBERCULOSIS - MORBIDITY AND MORTALITY OF A WORLDWIDE EPIDEMIC [J].
RAVIGLIONE, MC ;
SNIDER, DE ;
KOCHI, A .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1995, 273 (03) :220-226
[42]   Cutting edge:: Toll-like receptor (TLR)2- and TLR4-mediated pathogen recognition in resistance to airborne infection with Mycobacterium tuberculosis [J].
Reiling, N ;
Hölscher, C ;
Fehrenbach, A ;
Kröger, S ;
Kirschning, CJ ;
Goyert, S ;
Ehlers, S .
JOURNAL OF IMMUNOLOGY, 2002, 169 (07) :3480-3484
[43]   CHEMOKINE RESPONSE IN MICE INFECTED WITH MYCOBACTERIUM-TUBERCULOSIS [J].
RHOADES, ER ;
COOPER, AM ;
ORME, IM .
INFECTION AND IMMUNITY, 1995, 63 (10) :3871-3877
[44]   Mycobacterium tuberculosis:: Here today, and here tomorrow [J].
Russell, DG .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2001, 2 (08) :569-577
[45]   Chemokines induced by infection of mononuclear phagocytes with mycobacteria and present in lung alveoli during active pulmonary tuberculosis [J].
Sadek, MI ;
Sada, E ;
Toossi, Z ;
Schwander, SK ;
Rich, EA .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1998, 19 (03) :513-521
[46]   MILIARY TUBERCULOSIS [J].
SAHN, SA ;
NEFF, TA .
AMERICAN JOURNAL OF MEDICINE, 1974, 56 (04) :495-505
[47]   β-Cchemokines are induced by Mycobacterium tuberculosis and inhibit its growth [J].
Saukkonen, JJ ;
Bazydlo, B ;
Thomas, M ;
Strieter, RM ;
Keane, J ;
Kornfeld, H .
INFECTION AND IMMUNITY, 2002, 70 (04) :1684-1693
[48]   CD4 is required for the development of a protective granulomatous response to pulmonary tuberculosis [J].
Saunders, BM ;
Frank, AA ;
Orme, IM ;
Cooper, AM .
CELLULAR IMMUNOLOGY, 2002, 216 (1-2) :65-72
[49]  
Sauty A, 1999, J IMMUNOL, V162, P3549
[50]   Depletion of CD4+ T cells causes reactivation of murine persistent tuberculosis despite continued expression of interferon γ and nitric oxide synthase 2 [J].
Scanga, CA ;
Mohan, VP ;
Yu, KM ;
Joseph, H ;
Tanaka, K ;
Chan, J ;
Flynn, JL .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (03) :347-358