Mycobacterium tuberculosis induces apoptosis in γ/δ T lymphocytes from patients with advanced clinical forms of active tuberculosis

Clinical and Diagnostic Laboratory Immunology

Volumn 4, Issue 1, 1997, Pages 14-18

  Duarte, Rafael ^a   Kindlelán, José María ^a   Carracedo, Julia ^a   Sanchez Guijo, Pedro ^a   Ramírez, Rafael ^a  

^a HOSPITAL UNIVERSITARIO REINA SOFÍA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

RECOMBINANT INTERLEUKIN 2; T LYMPHOCYTE RECEPTOR;

ADULT; APOPTOSIS; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; HUMAN; HUMAN CELL; LYMPHOCYTE PROLIFERATION; MYCOBACTERIUM TUBERCULOSIS; PRIORITY JOURNAL; T LYMPHOCYTE SUBPOPULATION; TUBERCULOSIS;

EID: 0031051574     PISSN: 1071412X     EISSN: None     Source Type: Journal    
DOI: 10.1128/cdli.4.1.14-18.1997     Document Type: Article

References (25)

1. Agostini, C., R. Zambello, L. Trentin, A. Cerutti, P. Bullian, C. Crivellaro, A. Cipriani, and G. Semenzato. 1994. γ/δ T cell receptor subsets in the lung of patients with HIV-1 infection. Cell. Immunol. 153:194-205.
2. Barnes, P. E., C. L. Grisso, J. S. Abrams, H. Band, T. H. Rea, and R. L. Modlin. 1992. γ/δ T lymphocytes in human tuberculosis. J. Infect. Dis. 165: 506-512.
3. Boom, W. H., K. A. Chevernak, M. A. Mincek and J. J. Ellner. 1992. Role of mononuclear phagocyte as an antigen-presenting cell for human γδ cells activated by live Mycobacterium tuberculosis. Infect. Immunol. 60:3480-3488.
4. Constant, P., F. Davodeau, M. A. Peyrat, Y. Poquet, G. Puzo, M. Bonneville, and J. J. Fournié. 1994. Stimulation of human γδ T cells by nonpeptidic mycobacterial ligands. Science 264:267-270.
5. Crispe, N. 1989. Mechanism of self-tolerance. Immunol. Today 9:329-331.
6. a anergy in vivo. J. Immunol. 146:2083-2087
7. Dannenberg, A. M., Jr. 1991. Delayed-type hypersensitivity and cell-mediated immunity in the pathogenesis of tuberculosis. Immunol. Today 12:346-348.
8. De Libero, G., G. Casorati, C. Giachino, C. Carbonara, N. Migone, P. Matzinger, and A. Lanzavecchia. 1991. Selection by two powerful antigens may account for the presence of the population of human peripheral γδ T cells. J. Exp. Med. 173:1311-1322.
9. Drade, C. G., and B. L. Kotzin. 1992. Superantigens: biology, immunology and potential role in disease. J. Clin. Immunol. 12:149-162.
10. Gambon-Deza, F., M. Pacheco Carracedo, T. Cerda Mota, and J. Montes Santiago. 1995. Lymphocyte populations during tuberculosis infection: Vβ repertoires. Infect. Immun. 63:1235-1240.
11. Groh, V., S. Porcelli, M. Fabbi, L. L. Lanier, L. J. Picker, T. Anderson, R. A. Warnke, A. K. Bhan, J. L. Stromiriger, and M. B. Brenner. 1989. Human lymphocytes bearing T cell receptor γ/δ are phenotypically diverse and evenly distributed throughout the lymphoid system. J. Exp. Med. 169:1277-1294.
12. Haas, W., P. Pereira, and S. Tonegawa. 1993. Gamma/delta cells. Annu. Rev. Immunol. 11:637-685.
13. Havlir, D. V., J. J. Ellnèr, K. A. Chevernak, and W. H. Boom. 1991. Selective expansion of human γδ T cells by monocytes infected with live Mycobacterium tuberculosis. J. Clin. Invest. 87:729-733.
14. Hochstenbach, F., and M. B. Brenner. 1989. Newly identified γ/δ and β/δ T cell receptors. J. Clin. Immunol. 10:1-18.
15. Ingnatowicz, L., J. Kappler, and P. Marrack. 1992. The effect of chronic infection with a superantigen-producing virus. J. Exp. Med. 175:917-923.
16. Ito, M, N. Kojiro, T. Ikeda, T. Ito, J. Funada, and T. Kokubo. 1992. Increased proportions of peripheral blood γδ T cells in patients with pulmonary tuberculosis. Chest 102:195-197.
17. Jouvin-Marche, E., P. A. Cazenave, D. Voegtle, and P. N. Marche. 1992. Vβ17 T-cell deletion by endogenous mammary tumor virus in wild-typederived mouse strain. Proc. Natl. Acad. Sci. USA 89:3232-3235.
18. Kabelitz, D., A. Bender, T. Prospero, S. Wesselborg, O. Janssen, and K. Pechhold. 1991. The primary response of human γδ T cells to Mycobacierium tuberculosis is restricted to Vδ9-bearing cells. J. Exp. Med. 173:1331-1338.
19. Ladel, C. H., J. Hess, S. Daugelat, P. Mombaerts, S. Tonegawa, and S. H. E. Kaufmann. 1995. Contribution of α/β and γ/δ T lymphocytes to immunity against Mycobacterum bovis bacillus Calmette-Guerin: studies with T cell receptor-deficient mutant mice. Eur. J. Immunol. 25:838-846.
20. Lyons Bruce, A., K. Samuel, A. Sanderson, and A. H. Maddy. 1992. Simultaneous analysis of immunophenotype and apoptosis of murine thymocytes by single laser flow cytometry. Cytometry 13:809-821.
21. National Tuberculosis and Respiratory Disease Association. 1969. Diagnostic standards and classification of tuberculosis. National Tuberculosis and Respiratory Disease Association, New York, N.Y.
22. Ohmen, J. D., P. F. Barnes, K. Uyemura, S. Lu, C. L. Grisso, and R. L. Modlin. 1991. The T-cell receptors of human γδ T cells reactive to Mycobacterium tuberculosis are encoded by specific V genes but diverse V-J June-tions. J. Immunol. 147:3353-3359.
23. Panchamoorthy, G., J. McLean, R. L. Modlin, C. T. Morita, S. Ishikawa, M. B. Brenner, and H. Band. 1991. A predominance of the T-cell receptor Vγ2/Vδ2 subset in human mycobacteria-responsive T cells suggests germline gene encoded recognition. J. Immunol. 147:3360-3369.
24. Pfeffer, K., B. Schoel, N. Plesnila, G. B. Lipford, S. Kromer, K. Deusch, and H. Wagner. 1992. A lectin-binding, protease-resistant mycobacterial ligand specifically activates Vγ9+ human γδ cells. J. Immunol. 148:575-583.
25. Sperling, A. I., P. S. Linsley, A. B. Terrance, and J. A. Bluestone. 1993. CD28-mediated costimulation is necessary for the activation of T cell rceeptor-γδ lymphocytes. J. Immunol. 151:6043-6050.