The importance of gdT cells in the resolution of pathogen-induced inflammatory immune responses

Immunological Reviews

Volumn 173, Issue , 2000, Pages 98-108

  Carding, Simon R ^a,b   Egan, Paul J ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b UNIVERSITY OF LEEDS   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIAL INFECTION; CELL INTERACTION; CYTOTOXIC T LYMPHOCYTE; IMMUNE RESPONSE; INFECTION; INFLAMMATION; MACROPHAGE; PRIORITY JOURNAL; REVIEW; T LYMPHOCYTE; T LYMPHOCYTE ACTIVATION; VIRUS INFECTION; ANIMAL; BIOLOGICAL MODEL; HUMAN; IMMUNOLOGY; INFLUENZA; MOUSE;

LYMPHOCYTE ANTIGEN RECEPTOR;

ANIMALS; BACTERIAL INFECTIONS; HUMANS; INFLAMMATION; INFLUENZA, HUMAN; MICE; MODELS, IMMUNOLOGICAL; RECEPTORS, ANTIGEN, T-CELL, GAMMA-DELTA; T-LYMPHOCYTES;

EID: 0033621917     PISSN: 01052896     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1600-065X.2000.917302.x     Document Type: Review

References (48)

1. 1. Haslett C. The paradox of inflammation. Cell Biol 1995;6:315-316.
2. 2. Nagata S. Apoptosis by death factor. Cell 1997;88:355-365.
3. 3. Savill J. Apoptosis in resolution of inflammation. J Leukoc Biol 1997;61:375-380.
4. 4. Born W, Cady C, Jones-Carson J, Mukasa A, Lahn M, O'Brien R. Immunoregulatory functions of γδ T cells. Adv Immunol 1999;71:77-144.
5. 5. Doherty PC, Eichelberger M, Allan W, Carding SR. Roles of αβ and γδ T cell subsets in viral immunity. Annu Rev Immunol 1992;10:123-151.
6. 6. Haas W, Pereira P, Tonegawa S. γ/δ cells. Annu Rev Immunol 1993;11:637-685.
7. 7. Doherty PC, Allan W, Eichelberger M, Carding SR. Heat shock proteins and the γδ T cell response in virus infections. Springer Semin Immunopathol 1991;13:11-24.
8. - γδ T cells recovered from mice with influenza pneumonia. J Immunol 1991;147:2069-2074.
9. 9. Ponniah S, Doherty PC, Eichelberger M. Selective response of γδ T-cell hybridomas to orthomyxovirus-infected cells. J Virol 1996;70:17-22.
10. + T cells. J Exp Med 1990;172:1225-1231.
11. 11. O'Brien RL, et al. Heat shock protein Hsp60-reactive γδ cells: a large, diversified T-lymphocyte subset with highly focused specificity. Proc Natl Acad Sci USA 1992;89:4348-4352.
12. 12. Carding SR, Allan W, McMickle A, Doherty PC. Activation of cytokine genes in T cells during primary and secondary murine influenza pneumonia. J Exp Med 1993;177:475-482.
13. + T cell depletion. Reg Immunol 1993;5:142-150.
14. 14. Sciammas R, et al. Unique antigen recognition by a herpesvirus-specific TCR-γδ cell. J Immunol 1994;152:5392-5397.
15. 15. Sciammas R, Kodukula P, Tang Q, Hendricks RL, Bluestone JA. T cell receptor-γδ T cells protect mice from herpes simplex virus type 1-induced lethal encephalitis. J Exp Med 1997;185:1969-1975.
16. 16. Janeway CA Jr, Jones B, Hayday AC. Specificity and function of T cells bearing γδ receptors. Immunol Today 1988;9:73-76.
17. 17. Peng SL, Madaio MP, Hayday AC, Craft J. Propagation and regulation of systemic autoimmunity by γδ T cells. J Immunol 1996;157:5689-5698.
18. 18. Hou S, Katz JM, Doherty PC, Carding SR. Extent of γδ T cell involvement in the pneumonia caused by Sendai virus. Cell Immunol 1992;143:183-188.
19. + cells are a major component of the γδ T cell response to Listeria monocytogenes. J Immunol 1996;156:4280-4289.
20. 20. Belles C, Kuhl A, Nosheny R, Carding SR. Plasma membrane expression of heat shock protein 60 (Hsp60) in vivo in response to infection. Infect Immun 1999;67:4191-4200.
21. 21. Born W, Kelly KA, O'Brien R. In: Snow EC, ed. Handbook of B and T lymphocytes. San Diego: Academic Press; 1994:179-214.
22. 22. Ogasawara T, et al. Sendai virus pneumonia: evidence for the early recruitment of γδ T cells during the disease course. J Virol 1994;68:4022-4027.
23. 23. Hiromatsu K, et al. A protective role of γδ T cells in primary infection with Listeria monocytogenes in mice. J Exp Med 1992;175:49-56.
24. 24. Ohga S, Yoshikai Y, Takeda Y, Muramori K, Nomoto K. Sequential apperance of γδ and αβ-bearing T cells in the peritoneal cavity during i.p. infection with Listeria monocytogenes. Eur J Immunol 1990;20:533-540.
25. 25. Wallace M, Malkovsky M, Carding SR. γ/δ T lymphocytes in viral infections. J Leuk Biol 1995;58:277-283.
26. 26. Mukasa A, Hiromatsu K, Matsuzaki G, O'Brien R, Born W, Nomoto K. Bacterial infection of the testis leading to autoagressive immunity triggers apparently opposed responses of αβ and γδ T cells. J Immunol 1995;155:2047-2056.
27. 27. Fu Y-X, et al. Immune protection and control of inflammatory tissue necrosis by γδ T cells. J Immunol 1994;153:3101-3115.
28. 28. Mombaerts P, Arnoldi J, Russ F, Tonegawa S, Kaufmann SHE. Different roles of αβ and γδ T cells in immunity against an intracellular bacterial pathogen. Nature 1993;365:53-56.
29. + deficient mice display abnormal but distinct phenotypes towards a natural, widespread infection of the intestinal epithelium. Proc Nad Acad Sci USA 1996;93:11774-11779.
30. 30. DiTirro J, et al. Disruption of cellular inflammatory response to Listeria monocytogenes infection in mice with disruptions in targeted genes. Infect Immun 1998;66:2284-2289.
31. 31. Boom WH, Chervenak KA, Mincek MA, Ellner JJ. Role of the mononuclear phagocyte as an antigen-presenting cell for human γδ T cells activated by live Mycobacteria tuberculosis. Infect Immun 1992;60:3480-3487.
32. 32. Skeen MJ, Ziegler HK. Induction of murine peritoneal γδ T cells and their role in resistance to bacterial infection. J Exp Med 1993;178:971-978.
33. 33. Ferrick DA, Schrenzel MD, Mulvania T, Hsieh B, Ferlin WG, Lepper H. Differential production of Interferon-γ and interleukin-4 in response to Th1-and Th2-stimulating pathogens by γδ T cells in vivo. Nature 1995;373:255-257.
34. + T cells is activated by Mycobacterium tuberculosis but not by its 65-kDa heat shock protein. J Exp Med 1990;171:667-674.
35. 35. Peffer K, Schoel B, Gulle H, Kaufmann SHE, Wanger H. Primary responses of human T cells to mycobacteria: a frequent set of γδ T cells are stimulated by protease-resistant ligands. Eur J Immunol 1990;20:1175-1184.
36. 36. Kabelitz D, Bender A, Prospero T, Wesselborg S, Janssen O, Pechold K. The primary response of human γδ T cells to Mycobacterium tuberculosis is restricted to Vγ9-bearing cells. J Exp Med 1991;173:1331-1337.
37. 37. Panchamoorthy G, et al. A predominance of the T cell receptor Vγ2/Vδ2 subset in human mycobacteria-responsive T cells suggests germline gene encoded recognition. J Immunol 1991;147:3360-3366.
38. 38. Haregewoin A, Soman G, Hom RC, Finberg RW. Human γδ T cells respond to mycobacterial heat shock protein. Nature 1989;340:309-311.
39. 39. Munk ME, Gatrill AJ, Kaufmann SHE. In vitro activation of human γδ T cells by bacteria: evidence for specific interleukin secretion and target cell lysis. Curr Top Microbiol Immunol 1991;173:159-165.
40. 40. Morita CT, Lee HK, Leslie DS, Tanaka Y, Buckowski JF, Marker-Hermann E. Recognition of nonpeptide prenyl pyrophosphate antigens by human γδ T cells. Microbes and Infection 1999;1:175-186.
41. 41. Balaji K, Schwander SK, Rich EA, Boom WH. Alveolar macrophages as accessory cells for human γδ T cells activated by Mycobacterium tuberculosis. J Immunol 1995;154:5959-5968.
42. 42. Li B, et al. Disease-specific changes in γδ T cell repertoire and function in patients with pulmonary tuberculosis. J Immunol 1996;157:4222-4229.
43. 43. Li B, et al. Involvement of Fas/Fas-ligand pathway in activation-induced cell death of mycobacteria-reactive human γδ T cells: a mechanism for the loss of γδ T cells in patients with pulmonary tuberculosis. J Immunol 1998;161:1558-1567.
44. 44. D'Souza CD, Cooper AM, Frank AA, Mazzaccaro RJ, Bloom BR, Orme IM. An anti-inflammatory role for γδ T lymphocytes in acquired immunity to Mycobacterium tuberculosis. J Immunol 1997;158:1217-1221.
45. 45. Viitanen PV, Gatenby AA, Lorimer GH. Purified chaperonin 60 (groEL) interacts with the nonnative states of a multitude of Esherichia coli proteins. Protein Sci 1992;1:363-369.
46. 46. Lin T, et al. Fas ligand-mediated killing by intestinal intraepithelial lymphocytes. Participation in intestinal graft versus host disease. J Clin Invest 1998;101:570-577.
47. 47. Zeine R, Pon R, Ladiwala U, Antel JP, Filion LG, Freedman MS. Mechanism of γδ T cell-induced human oligodendrocyte cytotoxicity: relevance to multiple sclerosis. J Neuroimmunol 1998;87:49-61.
48. 48. Tough DF, Sprent J. Lifespan of γδ T cells. J Exp Med 1998;187:357-365.