Memory T Cell Development in the Absence of Specific Antigen Priming

Journal of Immunology

Volumn 157, Issue 12, 1996, Pages 5300-5307

  Lee, William T ^a,c   Cole Calkins, Jocelyn ^a   Street, Nancy E ^b  

^a STATE UNIVERSITY OF NEW YORK   (United States)

^b UNIVERSITY OF TEXAS AT DALLAS   (United States)

^c WADSWORTH CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CD45 ANTIGEN; ENTEROTOXIN; ENTEROTOXIN B, STAPHYLOCOCCAL; OVALBUMIN;

ANIMAL; ARTICLE; BAGG ALBINO MOUSE; CD4+ T LYMPHOCYTE; CELL SEPARATION; FEMALE; FLOW CYTOMETRY; IMMUNOLOGICAL MEMORY; IMMUNOLOGY; LYMPHOCYTE ACTIVATION; MOUSE; T LYMPHOCYTE SUBPOPULATION;

ANIMALS; ANTIGENS, CD45; CD4-POSITIVE T-LYMPHOCYTES; CELL SEPARATION; ENTEROTOXINS; FEMALE; FLOW CYTOMETRY; IMMUNOLOGIC MEMORY; LYMPHOCYTE ACTIVATION; MICE; MICE, INBRED BALB C; OVALBUMIN; T-LYMPHOCYTE SUBSETS;

EID: 0030589298     PISSN: 00221767     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (59)

1. Vitetta, E. S., E. Berton, M. T., C. Burger, M. Kepron, W. T. Lee, and X. M. Yin. 1991. Memory T and B cells. Annu. Rev. Immunol. 9:193.
2. Swain, S. L. 1995. CD4 T cell development and cytokine polarization: an overview. J. Leukocyte Biol. 57:795.
3. + T cell subsets: lymphokine secretion of memory cells and of effector cells that develop from precursors in vitro. J. Immunol. 144:1788.
4. Swain, S. L., L. M. Bradley, M. Croft, S. Tonkonogy, G. Alkins, A. Weinberg, D. D. Duncan, S. M. Hedrick, R. W. Dutton, and G. Huston. 1991. Helper T cell subsets: phenotype, function and the role of lymphokines in regulating their development. Immunol. Rev. 123:115.
5. Bradley, L. M., K. Yoshimoto, and S. L. Swain. 1995. The cytokines IL-4, IFN-gamma, and IL-12 regulate the development of subsets of memory effector helper T cells in vitro. J. Immunol. 155:1713.
6. + T cells. Annu. Rev. Immunol. 12:635.
7. + cells from T cell receptor transgenic mice. J. Exp. Med. 176:1091.
8. + T cells in vitro: characteristics and antigen-presenting cell requirements. J. Exp. Med. 176:1431.
9. + T cells through IL-12 produced Listeria-induced macrophages. Science 260:547.
10. Kearney, E. R., K. A. Pape, D. Y. Loh, and M. K. Jenkins. 1994. Visualization of peptide-specific immunity and peripheral tolerance induction in vivo. Immunity 1:327.
11. Swain, S. L. 1994. Generation and in vivo persistence of polarized Th1 and Th2 memory cells. Immunity 1:543.
12. Sanders, M. E., J. W. Makgoba, and S. Shaw. 1988. Human naive and memory T cells: reinterpretation of helper-inducer and suppressor-inducer subsets. Immunol. Today 9:195.
13. + phenotype. J. Exp. Med. 169:653.
14. + T cells. J. Immunol. 144:3288.
15. + memory T-cells from the spleen lack MEL-14, the lymph node homing receptor. J. Immunol. 148:324.
16. Sparshott, S. M., E. B. Bell, and S. R. Sarawar. 1991. CD45R CD4 T cell subset-reconstituted nude rats: subset-dependent survival of recipients and bi-directional isoform switching. Eur. J. Immunol. 21:993.
17. lo cells are memory cells. Cell. Immunol. 130:459.
18. Sanders, M. E., M. W. Makgoba, C. H. June, H. A. Young, and S. Shaw. 1989. Enhanced responsiveness of human memory T cells to CD2 and CD3 receptor-mediated activation. Eur. J. Immunol. 19:803.
19. + T lymphocytes. Immunol. Today 9:268.
20. Lee, W. T., and E. S. Vitetta. 1991. Virgin T cells do not provide help for antigen-specific B cells in the absence of IL-4, IL-5 and IL-6. Int. Immunol. 3:907.
21. lo thymocytes in vivo. Science 250: 1720.
22. White, J., K. M. Haskins, P. Marrack, and J. Kappler. 1983. Use of I region-restricted, antigen-specific T cell hybridomas to produce idiotypically specific anti-receptor antibodies. J. Immunol. 130:1033.
23. Janeway, C. A., Jr., J. Yagi, P. J. Conrad, M. E. Katz, B. Jones, S. Vroegop, and S. Buxser. 1989. T-cell responses to Mls and to bacterial proteins that mimic its behavior. Immunol. Rev. 107:61.
24. White, J., A. Herman, A. M. Pullen, R. Kubo, J. W. Kappler, and P. Marrack. 1989. The V-specific superantigen staphylococcal enterotoxin B: stimulation of mature T cells and clonal deletion in neonatal mice. Cell 56:27.
25. Padovan, E., G. Casorati, P. Dellabona, S. Meyer, M. Brockhaus, and A. Lanzavecchia. 1993. Expression of two T cell receptor α chains: dual receptor T cells. Science 262:422.
26. Padovan, E., C. Giachino, M. Cella, S. Valitutti, O. Acuto, and A. Lanzavecchia. 1995. Normal T lymphocytes can express two different T cell receptor β chains: implications for the mechanism of allelic exclusion. J. Exp. Med. 181:1587.
27. Dialynas, D. P., D. B. Wilde, P. Marrack, A. Pierres, K. A. Wall, W. Havran, G. Otten, M. R. Loken, M. Pierres, J. Kappler, and F. W. Fitch. 1983. Characterization of the murine antigenic determinant, designated L3T4a, recognized by monoclonal antibody GK1.5: expression of L3T4a by functional T cell clones appears to correlate primarily with class II MHC antigen-reactivity. Immunol. Rev. 74:29.
28. Logdberg, L., P. Wassmer, and E. M. Shevach. 1985. Role of the L3T4 antigen in T-cell activation. I. Description of a monoclonal IgM antibody to a distinct epitope (L3T4b) of the L3T4 antigen and its effect on interleukin 1-induced thymocyte proliferation. Cell. Immunol. 94:299.
29. Sarmiento, M., A. L. Glasebrook, and F. W. Fitch. 1980. IgG or IgM monoclonal antibodies reactive with different determinants on the molecular complex bearing Lyt-2 antigen block T cell-mediated cytolysis in the absence of complement. J. Immunol. 125:2665.
30. Springer, T., G. Galfre, D. S. Secher, and C. Milstein. 1978. Monoclonal xenogeneic antibodies to murine cell surface antigens: identification of novel leukocyte differentiation antigens. Eur. J. Immunol. 8:539.
31. Bruce, J., F. W. Symington, J. McKearn, and J. Sprent. 1981. A monoclonal antibody discriminating between subsets of T and B cells. J. Immunol. 127:2446.
32. Marshak-Rothstein, A., P. Fink, T. Gridley, D. H. Raulet, M. J. Bevans, and M. L. Gefter. 1979. Properties and applications of monoclonal antibodies directed against determinants on the Thy-1 locus. J. Immunol. 122:2491.
33. Bazin, H., L. Xhurdebise, G. Burtonboy, A. LeBacq, L. De Clercq, and F. Cormont. 1984. Rat monoclonal antibodies. I. Rapid purification from in vitro culture supernatants. J. Immunol. Methods 66:261.
34. H2 clones revealed by RNA hybridization, functionally monospecific bioassays and monoclonal antibodies. J. Exp. Med. 166:1229.
35. Staerz, U. D., H. G. Rammensee, J. D. Benedetto, and M. J. Bevan. 1985. Characterization of a murine monoclonal antibody specific for an allotypic determinant on T cell antigen receptor. J. Immunol. 134:3994.
36. Haskins, K., R. Kubo, J. White, M. Pigeon, J. Kappler, and P. Marrack. 1983. The major histocompatibility complex-restricted antigen receptor on T cells. I. Isolation with a monoclonal antibody. J. Exp. Med. 157:1149.
37. Lee, W. T., and E. S. Vitetta. 1992. Memory T cells are anergic to the superantigen, staphylococcal enterotoxin B. J. Exp. Med. 176:575.
38. Myers, C. D., V. M. Sanders, E. Yefenof, K. G. Oliver, J. W. Uhr, and E. S. Vitetta. 1987. Purification and characterization of antigen-binding virgin and memory B cells. Methods Enzymol. 150:316.
39. Hoag, K. A., N. E. Street, G. B. Huffnagle, and M. F. Lipscomb. 1995. Early cytokine production in pulmonary Cryptococcus neaformans infections distinguishes susceptible and resistant mice. Am. J. Respir. Cell Mol. Biol. 13:487.
40. + effector T-cells in vivo: immunization results in a transient population of MEL-14-, CD45RB-helper cells that secretes interleukin-2 (IL-2), IL-3, IL-4, and interferon-gamma. J. Exp. Med. 174:547.
41. Croft, M., and S. L. Swain. 1991. B cell response to fresh and effector T helper cells: role of cognate T-B interaction and the cytokines IL-2, IL-4, and IL-6. J. Immunol. 146:4055.
42. + T cells: ICAM-1 or B7-1 can costimulate naive CD4 T cell activation but both are required for optimum response. J. Immunol. 155:45.
43. Farber, D. L., M. Luqman, O. Acuto, and K. Bottomly. 1995. Control of memory CD4 T cell activation: MHC class II molecules on APCs and CD4 ligation inhibit memory but not naive CD4 cells. Immunity 2:249.
44. 1. J. Exp. Med. 162:1726.
45. Snapper, C. M., and W. E. Paul. 1987. Interferon-gamma and B cell stimulatory factor-1 reciprocally regulate Ig isotype production. Science 236:944.
46. Heath, W. R., F. R. Carbone, P. Bertolino, J. Kelly, S. Cose, and J. F. A. P. Miller. 1995. Expression of two T cell receptor α chains on the surface of normal murine T cells. Eur. J. Immunol. 25:1617.
47. Lassila, O., O. Vainio, and P. Matzinger. 1988. Can B cells turn on virgin T cells? Nature 334:253.
48. Uematsu, Y., S. Ryser, Z. Dembic, P Borgulya, P. Krimpenfort, A. Berns, H. von Boehmer, and M. Steinmetz. 1988. In transgenic mice the introduced functional T cell receptor β gene prevents expression of endogenous β genes. Cell 52:831.
49. Elliott, J. I., and D. M. Altmann. 1995. Dual T cell receptor α chain T cells in autoimmunily. J. Exp. Med. 182:953.
50. Hardardottir, F., J. L. Baron, and C. A. Janeway, Jr. 1995. T cells with two functional antigen-specific receptors. Proc. Natl. Acad. Sci. USA 92:354.
51. Sprent, J. 1994. T and B memory cells. Cell 76:315.
52. Croft, M., L. M. Bradley, and S. L. Swain. 1994. Naive versus memory CD4 T cell response to antigen: memory cells are less dependent on accessory cell co-stimulation and can respond to many antigen-presenting cell types including resting B cells. J. Immunol. 152:2675.
53. Mackay, C. R., W. L. Marston, and L. Dudler. 1990. Naive and memory T cells show distinct pathways of lymphocyte recirculation. J. Exp. Med. 171:801.
54. Kaye, J., and S. M. Hedrick. 1988. Analysis of specificity for antigen, Mls, and allogeneic MHC by transfer of T-cell receptor α- and β-chain genes. Nature 336:580.
55. + T helper cell phenotype development in a T cell receptor-αβ-transgenic model. J. Exp. Med. 182:1579.
56. + T cells. J. Exp. Med. 182:1591.
57. Duncan, D. D., and S. L. Swain. 1994. Role of antigen-presenting cells in the polarized development of helper T cell subsets: evidence for differential cytokine production by Th0 cells in response to antigen presentation by B cells and macrophages. Eur. J. Immunol. 24:2506.
58. Koch, S., G. Muralidhar, and S. L. Swain. 1994 Both naive and memory CD4 T cell subsets become anergic during MAIDS and each subset can sustain disease. J. Immunol. 152:5548.
59. Lafaille, J. J., K. Nagashima, M. Katsuki, and S. Tonegawa. 1994. High incidence of spontaneous autoimmune encephalomyelitis in immunodeficient anti-myelin basic protein T cell receptor transgenic mice. Cell 78:399.