TCR αβ+ CD4- CD8- T cells differentiate extrathymically in an lck-independent manner and participate in early response against Listeria manocytogenes infection through interferon-γ production

Immunology

Volumn 91, Issue 4, 1997, Pages 511-519

  Kadena, T ^a   Matsuzaki, G ^a   Fujise, S ^a   Kishihara, K ^a   Takimoto, H ^a   Sasaki, M ^a   Beppu, M ^a   Nakamura, S ^a   Nomoto, K ^a  

^a KYUSHU UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CD4 ANTIGEN; CD8 ANTIGEN; GAMMA INTERFERON; GRANULOCYTE MACROPHAGE COLONY STIMULATING FACTOR; INTERLEUKIN 4; MACROPHAGE CHEMOTACTIC FACTOR; T LYMPHOCYTE RECEPTOR;

ANIMAL EXPERIMENT; ARTICLE; CONTROLLED STUDY; FEMALE; HOST RESISTANCE; LISTERIA MONOCYTOGENES; LISTERIOSIS; LYMPHOCYTE DIFFERENTIATION; MACROPHAGE; MOUSE; NONHUMAN; PRIORITY JOURNAL; T LYMPHOCYTE SUBPOPULATION;

EID: 0030743779     PISSN: 00192805     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2567.1997.00303.x     Document Type: Article

References (42)

1. GRAY M.L. & KILLINGER A.H. (1966) Listeria monocytogenes and listeric infections. Bacteriol Rev 30, 309.
2. KAUFMANN S.H.E., SIMON M.M. & HAHN H. (1982) Regulatory interactions between macrophages and T-cell subsets in Listeria monocytogenes-specific T-cell activation. Infect Immun 38, 907.
3. MITSUYAMA M., TAKEYA K., NOMOTO K. & SHIMOTORI S. (1978) Three phases of phagocyte contribution to resistance against Listeria monocytogenes. J Gen Microbiol 106, 165.
4. MIYATA M., MITSUYAMA M., OGATA N. & NOMOTO K. (1984) Protective mechanisms against infection by Listeria monocytogenes: accumulation and activation of macrophages. J Clin Lab Immunol 13, 111.
5. MACKANESS G.B. (1962) Cellular resistance to infection. J Exp Med 116, 381.
6. REIMANN J. (1991) Double-negative (CD4 CD8 ), TCRαβ-expressing, peripheral T cells. Scand J Immunol 34, 679.
7. CRISPE I.N. (1994) CD4/CD8-negative T cells with αβ antigen receptors. Curr Opin Immunol 6, 438.
8. + thymocytes. J Immunol 146, 1113.
9. + cells. J Immunol 145, 3209.
10. IIAI T., WATANABE H., SEKI S. et al. (1992) Ontogeny and development of extrathymic T cells in mouse liver. Immunology 77, 556.
11. FOWLKS B.J., KRUISBEEK A.M., TON-THAT H. et al. (1987) A novel population of T-cell receptor αβ-bearing thymocytes which predominantly expresses a single Vβ gene family. Nature 329, 251.
12. BUDD R.C., MIESCHER G.C., HOWE R.C., LEES R.K., BRON C. & MACDONALD H.R. (1987) Developmentally regulated expression of T cell receptor β chain variable domains in immature thymocytes. J Exp Med 166, 577.
13. - cells. J Exp Med 179 1957.
14. + subset. J Immunol 145, 1039.
15. + cells. Eur J Immunol 22, 2929.
16. OHGA S., YOSHIKAI Y., TAKEDA Y., HIROMATSU K. & NOMOTO K. (1990) Sequential appearance of γ/δ- and α/β-bearing T cells in the peritoneal cavity during an i.p. infection with Listeria monocytogenes. Eur J Immunol 20, 533.
17. HIROMATSU K., YOSHIKAI Y., MATSUZAKI G. et al. (1992) A protective role of γ/δ T cells in primary infection with Listeria monocytogenes in mice. J Exp Med 175, 49.
18. MATSUZAKI G., HIROMATSU K., YOSHIKAI Y., MURAMORI K. & NOMOTO K. (1993) Characterization of T-cell receptor γδ T cells appearing at the early phase of murine Listeria manocytogenes infection. Immunology 78, 22.
19. - T cells with a skewed variable region repertoire after infection with Listeria monocytogenes. Eur J Immunol 25 1985.
20. lck. Nature 357, 161.
21. SONG F., MATSUZAKI G., MITSUYAMA M. & NOMOTO K. (1996) Differential effects of viable and killed bacteria on IL-12 expression of macrophages. J Immunol 156, 2979.
22. FERRICK D.A., SCHRENZEL M.D., MULVANIA T., HSIEH B., FERLIN W.G. & LEPPER H. (1995) Differential production of interferon-γ and interleukin-4 in response to Th1- and Th2-stimulating pathogens by γδ T cells in vivo. Nature 373, 255.
23. + cells responsible for acute marrow graft rejection are present in thymus-deficient mice. J Immunol 149, 403.
24. MAKINO Y., YAMAGATA N., SASHO T. et al. (1993) Extrathymic development of Vα14-positive T cells. J Exp Med 177, 1399.
25. - T cells with T cell receptor γ/δ or α/β after thymus grafting to nude mice: Influence of thymus on extrathymic T cell differentiation. Cell Immunol 153, 79.
26. SEKI S. ABO T., OHTEKI T., SUGIURA K. & KUMAGAI K. (1991) Unusual αβ-T cells expanded in autoimmune lpr mice are probably a counterpart of normal T cells in the liver. J Immunol 147, 1214.
27. int liver mononuclear cells. Eur J Immunol 25, 3365.
28. - T cells bearing αβ T cell receptor. J Immunol 142, 3773.
29. lck. Cell 55, 301.
30. SHAW A.S., AMREIN K.E., HAMMOND C., STERN D.F., SEFTON B.M. & ROSE J.K. (1989) The lck tyrosine protein kinase interacts with the cytoplasmic tail of the CD4 glycoprotein through its unique amino-terminal domain. Cell 59, 627.
31. lck with CD4 in antigen-specific signal transduction in T cells. Cell 64, 511.
32. lck. Identification of novel intermolecular association. Science 252, 1523.
33. lck. EMBO J 11, 4877.
34. lck in thymopoiesis. EMBO J 12, 1671.
35. - T cells produce IL-4. J Immunol 149, 1211.
36. KATSIKIS P.D., COHEN S.B.A., MURISON J.G. et al. (1995) Human αβ T-cell receptor CD4-CD8 T-cell clones are predominantly Th0-like. Immunology 84, 501.
37. + T cells are a potential source of IL-4 during primary immune response. J Immunol 155, 4544.
38. + T cells. Nature 372, 691.
39. DELLABONA P., CASORATI G., FRIEDLI B. et al. (1993) In vivo persistence of expanded clones specific for bacterial antigens within the human T cell receptor α/β CD4 8 subset. J Exp Med 177, 1763.
40. SIELING P.A., CHATTERJEE D., PORCELLI S.A. et al. (1995) CD1-restricted T cell recognition of microbial lipoglycan antigens. Science 269, 227.
41. NOMOTO K., TANIGUCHI K., KUBO C. & TAKEYA K. (1978) Relationships among differentiated T-cell subpopulations. III. Radioresistance of delayed hypersensitivity to heterologous erythrocytes. Immunology 34, 517.
42. NOMOTO K. (1987) Animal Models: Assessing the Scope of Their Use in Biomedical Research p.199. Alan R. Liss. Inc., New York.