Cytokine profiles in tuberculosis patients and healthy subjects in response to complex and single antigens of Mycobacterium tuberculosis

被引:38
作者
Al-Attiyah, Raja'a
Madi, Nada M.
El-Shamy, Abdul-salaam M.
Wiker, Harald G.
Andersen, Peter
Mustafa, Abu S.
机构
[1] Kuwait Univ, Fac Med, Dept Microbiol, Safat 13110, Kuwait
[2] Chest Dis Hosp, Minist Hlth, Kuwait, Kuwait
[3] Norwegian Inst Publ Hlth, Div Environm Med, Oslo, Norway
[4] Statens Serum Inst, Dept Infect Dis Immunol, DK-2300 Copenhagen, Denmark
来源
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY | 2006年 / 47卷 / 02期
关键词
cytokines; tuberculosis patients; healthy subjects; peripheral blood mononuclear cells; Mycobacterium tuberculosis antigens;
D O I
10.1111/j.1574-695X.2006.00110.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Peripheral blood mononuclear cells (PBMC) were obtained from tuberculosis (TB) patients and Mycobacterium bovis bacillus Calmette-Guerin vaccinated healthy subjects. PBMC were tested for secretion of tumor necrosis factor-oc JNF-alpha), interferon-gamma (IFN-gamma), interleukin-5 (IL-5) and IL-10 in response to complex (whole cells, culture filtrate and cell walls), single secreted (Ag85B, ESAT6, MPT64, PstS and MPT70) and single cytosolic (DnaK, GroES and GroEL antigens of Mycobacterium tuberculosis. In the absence of antigens, detectable concentrations of TNF-alpha, IFN-gamma and IL-10 were secreted by PBMC of both donor groups, but the concentrations of only IL-10 were significantly higher (P = 0.015) in TB patients than in healthy subjects. In the presence of complex antigens, PBMC secreted IFN-gamma and TNF-alpha in response to all three preparations, whereas IL-10 was secreted in response to whole cells and cell walls only. In the presence of single antigens, IFN-gamma was secreted in response to Ag85B, ESAT6 and MPT64 in TB patients and ESAT6 in healthy donors. Except for GroEL and DnaK, single antigens did not induce TNF-a and IL- 10 secretion from PBMC in either donor group. The secretion of IFN-gamma, but not IL- 10, in the presence of Ag85B, ESAT6 and MPT64 supports their potential as subunit vaccine candidates against TB.
引用
收藏
页码:254 / 261
页数:8
相关论文
共 42 条
[1]   Specific acquired resistance in mice immunized with killed mycobacteria [J].
Agger, EM ;
Weldingh, K ;
Olsen, AW ;
Rosenkrands, I ;
Andersen, P .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 2002, 56 (05) :443-447
[2]   Synthetic peptides identify promiscuous human Th1 cell epitopes of the secreted mycobacterial antigen MPB70 [J].
Al-Attiyah, R ;
Shaban, FA ;
Wiker, HG ;
Oftung, F ;
Mustafa, AS .
INFECTION AND IMMUNITY, 2003, 71 (04) :1953-1960
[3]   Evaluation of complex and defined antigens of Mycobacterium tuberculosis in an IgG-specific ELISA for the diagnosis of tuberculosis [J].
Amoudy, HA ;
AlAsmer, ABH ;
Abul, AT ;
Mustafa, AS .
MEDICAL PRINCIPLES AND PRACTICE, 1997, 6 (02) :103-109
[4]   TB subunit vaccines - putting the pieces together [J].
Andersen, P ;
Doherty, TM .
MICROBES AND INFECTION, 2005, 7 (5-6) :911-921
[5]  
ANDERSEN P, 1995, J IMMUNOL, V154, P3359
[6]   Morphometric analysis of Th1 and Th2 cytokine expression in human pulmonary tuberculosis [J].
Bai, XY ;
Wilson, SE ;
Chmura, K ;
Feldman, NE ;
Chan, ED .
TUBERCULOSIS, 2004, 84 (06) :375-385
[7]   Dysregulation of proinflammatory and regulatory cytokines in HIV infected persons with active tuberculosis [J].
Bal, AM ;
Lakhashe, SK ;
Thakar, MR ;
Tripathy, SP ;
Paranjape, RS .
CYTOKINE, 2005, 30 (05) :275-281
[8]   CYTOKINE PRODUCTION AT THE SITE OF DISEASE IN HUMAN TUBERCULOSIS [J].
BARNES, PF ;
LU, SZ ;
ABRAMS, JS ;
WANG, E ;
YAMAMURA, M ;
MODLIN, RL .
INFECTION AND IMMUNITY, 1993, 61 (08) :3482-3489
[9]  
Brandt L, 1996, J IMMUNOL, V157, P3527
[10]   T-cell responses to the Mycobacterium tuberculosis- specific antigen ESAT-6 in Brazilian tuberculosis patients [J].
Cardoso, FLL ;
Antas, PRZ ;
Milagres, AS ;
Geluk, A ;
Franken, KLMC ;
Oliveira, EB ;
Teixeira, HC ;
Nogueira, SA ;
Sarno, EN ;
Klatser, P ;
Ottenhoff, THM ;
Sampaio, EP .
INFECTION AND IMMUNITY, 2002, 70 (12) :6707-6714