T-cell responses to CD1-presented lipid antigens in humans with Mycobacterium tuberculosis infection

被引:128
作者
Ulrichs, T
Moody, DB
Grant, E
Kaufmann, SHE
Porcelli, SA
机构
[1] Yeshiva Univ Albert Einstein Coll Med, Dept Microbiol & Immunol, Bronx, NY 10461 USA
[2] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Rheumatol Immunol, Boston, MA 02115 USA
[3] Max Planck Inst Infect Biol, Dept Immunol, Berlin, Germany
关键词
D O I
10.1128/IAI.71.6.3076-3087.2003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CDI-restricted presentation of lipid or glycolipid antigens derived from Mycobacterium tuberculosis has been demonstrated by in vitro experiments using cultured T-cell lines. In the present work, the frequency of T-cell responses to natural mycobacterial lipids was analyzed in ex vivo studies of peripheral blood lymphocytes from human patients with pulmonary tuberculosis, from asymptomatic individuals with known contact with M. tuberculosis documented by conversion of their tuberculin skin tests, and from healthy tuberculin skin test-negative individuals or individuals vaccinated with Mycobacterium bovis BCG. Proliferation and gamma interferon enzyme-linked immunospot assays using peripheral blood lymphocytes and autologous CD1(+) immature dendritic cells revealed that T cells from asymptomatic M. tuberculosis-infected donors responded with significantly greater magnitude and frequency to mycobacterial lipid antigen preparations than lymphocytes from uninfected healthy donors. By use of these methods, lipid-antigen-specific proliferative responses were minimally detectable or absent in blood samples from patients with active tuberculosis prior to chemotherapy but became detectable in blood samples drawn 2 weeks after the start of treatment. Lipid antigen-reactive T cells were detected predominantly in the CD4-enriched T-cell fractions of circulating lymphocytes, and anti-CD1 antibody blocking experiments confirmed the CD1 restriction of these T-cell responses. Our results provide further support for the hypothesis that lipid antigens serve as targets of the recall response to M. tuberculosis, and they indicate that CDI-restricted T cells responding to these antigens comprise a significant portion of the circulating pool of M. tuberculosis-reactive T cells in healthy individuals with previous exposure to M. tuberculosis.
引用
收藏
页码:3076 / 3087
页数:12
相关论文
共 37 条
[21]   CD1B RESTRICTS THE RESPONSE OF HUMAN CD4-8- LYMPHOCYTES-T TO A MICROBIAL ANTIGEN [J].
PORCELLI, S ;
MORITA, CT ;
BRENNER, MB .
NATURE, 1992, 360 (6404) :593-597
[22]   The CD1 system: Antigen-presenting molecules for T cell recognition of lipids and glycolipids [J].
Porcelli, SA ;
Modlin, RL .
ANNUAL REVIEW OF IMMUNOLOGY, 1999, 17 :297-329
[23]   Mycobacterium tuberculosis 19-kilodalton lipoprotein inhibits Mycobacterium smegmatis-induced cytokine production by human macrophages in vitro [J].
Post, FA ;
Manca, C ;
Neyrolles, O ;
Ryffel, B ;
Young, DB ;
Kaplan, G .
INFECTION AND IMMUNITY, 2001, 69 (03) :1433-1439
[24]   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
[25]   CD8+ CTL from lungs of Mycobacterium tuberculosis-infected mice express perforin in vivo and Lyse infected macrophages [J].
Serbina, NV ;
Liu, CC ;
Scanga, CA ;
Flynn, JL .
JOURNAL OF IMMUNOLOGY, 2000, 165 (01) :353-363
[26]   Evidence for human CD4+ T cells in the CD1-restricted repertoire:: Derivation of mycobacteria-reactive T cells from leprosy lesions [J].
Sieling, PA ;
Ochoa, MT ;
Jullien, D ;
Leslie, DS ;
Sabet, S ;
Rosat, JP ;
Burdick, AE ;
Rea, TH ;
Brenner, MB ;
Porcelli, SA ;
Modlin, RL .
JOURNAL OF IMMUNOLOGY, 2000, 164 (09) :4790-4796
[27]   Self-recognition of CD1 by γ/δ T cells:: Implications for innate immunity [J].
Spada, FM ;
Grant, EP ;
Peters, PJ ;
Sugita, M ;
Melián, A ;
Leslie, DS ;
Lee, HK ;
van Donselaar, E ;
Hanson, DA ;
Krensky, AM ;
Majdic, O ;
Porcelli, SA ;
Morita, CT ;
Brenner, MB .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (06) :937-948
[28]   CD1d-restricted recognition of synthetic glycolipid antigens by human natural killer T cells [J].
Spada, FM ;
Koezuka, Y ;
Porcelli, SA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (08) :1529-1534
[29]  
Spada FM, 2000, EUR J IMMUNOL, V30, P3468, DOI 10.1002/1521-4141(2000012)30:12<3468::AID-IMMU3468>3.0.CO
[30]  
2-C