Down-regulation of T helper 1 responses to mycobacterial antigens due to maturation of dendritic cells by 10-kDa Mycobacterium tuberculosis secretory antigen

被引:32
作者
Natarajan, K
Latchumanan, VK
Singh, B
Singh, S
Sharma, P
机构
[1] Int Ctr Genet Engn & Biotechnol, Immunol Grp, New Delhi 110067, India
[2] All India Inst Med Sci, Dept Lab Med, New Delhi, India
关键词
D O I
10.1086/368173
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interactions of 10-kDa Mycobacterium tuberculosis secretory antigen (MTSA) with dendritic cells (DCs) were investigated to elucidate the role of secretory antigens in regulating immune responses to M. tuberculosis early in the course of infection. MTSA induced the maturation of different DC subsets. The cytokine profiles of these DCs were characteristic to each DC subset. Of interest, coculture of M. tuberculosis whole-cell extract (CE)-pulsed, MTSA-matured DCs with CE-specific T cells led to a marked reduction in interleukin (IL)-2 and interferon (IFN)-gamma production, thereby down-regulating proinflammatory responses to mycobacterial antigens. Attenuation of IL-2 and IFN-gamma levels of CE-specific T cells also was obtained when M. tuberculosis culture filtrate protein-activated DCs were employed as antigen-presenting cells, which suggests that MTSAs induce maturation of DCs at sites of infection, probably to down-regulate proinflammatory immune responses to mycobacteria that may subsequently be released from infected macrophages.
引用
收藏
页码:914 / 928
页数:15
相关论文
共 67 条
[31]   Evidence for occurrence of the ESAT-6 protein in Mycobacterium tuberculosis and virulent Mycobacterium bovis and for its absence in Mycobacterium bovis BCG [J].
Harboe, M ;
Oettinger, T ;
Wiker, HG ;
Rosenkrands, I ;
Andersen, P .
INFECTION AND IMMUNITY, 1996, 64 (01) :16-22
[32]  
Henderson RA, 1997, J IMMUNOL, V159, P635
[33]   Microbial lipopeptides stimulate dendritic cell maturation via toll-like receptor 2 [J].
Hertz, CJ ;
Kiertscher, SM ;
Godowski, PJ ;
Bouis, DA ;
Norgard, MV ;
Roth, MD ;
Modlin, RL .
JOURNAL OF IMMUNOLOGY, 2001, 166 (04) :2444-2450
[34]   Exploiting the immune system: Toward new vaccines against intracellular bacteria [J].
Hess, J ;
Schaible, U ;
Raupach, B ;
Kaufmann, SHE .
ADVANCES IN IMMUNOLOGY, VOL 75, 2000, 75 :1-88
[35]   Mycobacterium tuberculosis induces differential cytokine production from dendritic cells and macrophages with divergent effects on naive T cell polarization [J].
Hickman, SP ;
Chan, J ;
Salgame, P .
JOURNAL OF IMMUNOLOGY, 2002, 168 (09) :4636-4642
[36]   GENERATION OF LARGE NUMBERS OF DENDRITIC CELLS FROM MOUSE BONE-MARROW CULTURES SUPPLEMENTED WITH GRANULOCYTE MACROPHAGE COLONY-STIMULATING FACTOR [J].
INABA, K ;
INABA, M ;
ROMANI, N ;
AYA, H ;
DEGUCHI, M ;
IKEHARA, S ;
MURAMATSU, S ;
STEINMAN, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 176 (06) :1693-1702
[37]   OmpA targets dendritic cells, induces their maturation and delivers antigen into the MHC class I presentation pathway [J].
Jeannin, P ;
Renno, T ;
Goetsch, L ;
Miconnet, I ;
Aubry, JP ;
Delneste, Y ;
Herbault, N ;
Baussant, T ;
Magistrelli, G ;
Soulas, C ;
Romero, P ;
Cerottini, JC ;
Bonnefoy, JY .
NATURE IMMUNOLOGY, 2000, 1 (06) :502-509
[38]   T-cell priming by type-1 and type-2 polarized dendritic cells: the concept of a third signal [J].
Kalinski, P ;
Hilkens, CMU ;
Wierenga, EA ;
Kapsenberg, ML .
IMMUNOLOGY TODAY, 1999, 20 (12) :561-567
[39]  
Kamath AT, 1999, IMMUNOLOGY, V96, P511
[40]   Is the development of a new tuberculosis vaccine possible? [J].
Kaufmann, SHE .
NATURE MEDICINE, 2000, 6 (09) :955-960