Visualization, characterization, and turnover of CD8+ memory T cells in virus-infected hosts

Journal of Experimental Medicine

Volumn 183, Issue 4, 1996, Pages 1367-1375

  Zimmermann, Christine ^a   Brduscha Riem, Karin ^b   Blaser, Claudine ^a   Zinkernagel, Rolf M ^b   Pircher, Hanspeter ^a  

^a UNIVERSITY OF FREIBURG   (Germany)

^b UNIVERSITY OF ZURICH   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

CD8 ANTIGEN;

ADOPTIVE TRANSFER; ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CELL SURVIVAL; CONTROLLED STUDY; IMMUNOLOGICAL MEMORY; LYMPHOCYTIC CHORIOMENINGITIS VIRUS; MEMORY CELL; MOUSE; NONHUMAN; PRIORITY JOURNAL; TRANSGENIC MOUSE;

AMINO ACID SEQUENCE; ANIMALS; BIOLOGICAL MARKERS; CD8-POSITIVE T-LYMPHOCYTES; CYTOTOXICITY, IMMUNOLOGIC; FLOW CYTOMETRY; IMMUNOLOGIC MEMORY; IMMUNOTHERAPY, ADOPTIVE; LYMPHOCYTE ACTIVATION; LYMPHOCYTIC CHORIOMENINGITIS; MICE; MICE, INBRED C57BL; MICE, TRANSGENIC; MOLECULAR SEQUENCE DATA; PEPTIDE FRAGMENTS; RECEPTORS, ANTIGEN, T-CELL; SPLEEN; VIRAL PROTEINS;

EID: 0029961635     PISSN: 00221007     EISSN: None     Source Type: Journal    
DOI: 10.1084/jem.183.4.1367     Document Type: Article

References (48)

1. Cerottini, J.-C., and H.R. MacDonald. 1989. The cellular basis of T-cell memory. Annu. Rev. Immunol. 7:77-89.
2. Allouch, M., J.A. Owen, and P.C. Doherty. 1982. Limitdilution analysis of weak influenza-immune T cell responses associated with H-2Kb and H-2Db. J. Immunol. 129:689-693.
3. Moskophidis, D., U. Assmann-Wischer, M.M. Simon, and F. Lehmann Grube. 1987. The immune response of the mouse to lymphocytic choriomeningitis virus. V. High numbers of cytolytic T lymphocytes are generated in the spleen during acute infection. Eur J. Immunol. 17:937-942.
4. + T cells identified by expression of Pgp-1. J. Immunol. 138:3583-3586.
5. Sanders, M.S., M.W. Makgoba, S.O. Sharrow, D. Stephany, T.A. Springer, H.A. Young, and S. Shaw. 1988. Human memory T lymphocytes express increased levels of three cell adhesion molecules (LFA-3, CD2, and LFA-1) and three other molecules (UCHL1, CDw29, and Pgp-1) and have enhanced IFN-gamma production. J. Immunol. 140:1401-1407.
6. Inaba, K., and R.M. Steinman. 1984. Resting and sensitized T lymphocytes exhibit distinct stimulatory (antigen-presenting cell) requirements for growth and lymphokine release. J. Exp. Med. 160:1717-1735.
7. Fuchs, E.J., and P. Matzinger. 1992. B cells turn off virgin but not memory T cells. Science (Wash. DC). 258:1156-1159.
8. 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. 19:803-808.
9. Farber, D.L., M. Luqman, O. Acuto, and K. Bottomry. 1995. Control of memory CD4 T cell activation: MHC class II molecules on APCs and CD4 ligation inhibit memory but not naive CD4 T cells. Immunity. 2:249-259.
10. Bruno, L., J. Kirberg, and H. von Boehmer. 1995. On the cellular basis of immunological T cell memory Immunity. 2: 37-43.
11. Byrne, J.A., J.L. Butler, and M.D. Cooper. 1988. Differential activation requirements for virgin and memory T cells. J. Immunol. 141:3249-3257.
12. 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 costimulation and can respond to many antigen-presenting cell types including resting B cells. J. Immunol. 152:2675-2685.
13. + T cells differing in CD45R expression. J. Immunol 149:2300-2306.
14. + naive T cells can be efficiently activated by remote co-stimulation with B7. Int. Immunol. 5:1483-1487.
15. + T lymphocytes from TCR transgenic mice. J. Immunol 152:5220-5225.
16. Ehlers, S., and K.A. Smith. 1991. Differentiation of T cell Lymphokine gene expression: the in vitro acquisition of T cell memory. J. Exp. Med. 173:25-36.
17. + T cell clones. J. Immunol. 143:907-912.
18. + T cells. J. Immunol. 144:3288-3295.
19. + T lymphocytes different from unprimed cells? Eur. J. Immunol. 24:1073-1079.
20. Swain, S. 1994. Generation and in vivo persistence of polarized Th1 and Th2 memory cells. Immunity. 1:543-552.
21. Mackay, C.R. 1992. Immunological memory. Adv. Immunol. 53:217-265.
22. Bell, E.B., and S.M. Sparshotc. 1990. Interconversion of CD45R subsets of CD4 T cells in vivo. Nature (Lond.). 348: 163-165.
23. Michie, C.A., A. McLean, C. Alcock, and P.C.L. Beverley. 1992. Lifespan of human lymphocyte subsets defined by CD45 isoforms. Nature (Lond.). 360:264-265.
24. Celada, F. 1971. The cellular basis of the immunologic memory. Prog. Allergy. 15:223-267.
25. Lau, L.L., B.D. Jamieson, T. Somasundaram, and R. Ahmed_ 1994. Cytotoxic T-cell memory without antigen. Nature (Lond.) 369:648-652.
26. + T-cell memory determined by clonal burst size. Nature (Lond.). 369:652-654.
27. Mullbacher, A. 1994. The long-term maintenance of cytotoxic T cell memory does not require persistence of antigen. J. Exp. Med. 179:317-321.
28. Gray, D., and P. Matzinger. 1991. T cell memory is short-lived in the absence of antigen. J. Exp. Med. 174:969-974.
29. Oehen, S., H.P Waldner, T. Kündig, H. Hengartner, and R.M. Zinkemagel. 1992. Antivirally protective cytotoxic T cell memory to lymphocytic choriomeningitis virus is governed by persisting antigen J. Exp. Med. 176:1273-1281.
30. Selin, L.K., S.R. Nahill, and R.M. Welsh. 1994. Cross-reactivities in memory cytotoxic T lymphocyte recognition of heterologous viruses. J Exp. Med. 179:1933-1943.
31. Tough, D.F., and J. Sprent. 1994. Turnover of naive- and memory-phenotype T cells. J. Exp. Med. 179:1127-1135.
32. Schittek, B., and K. Rajewsky. 1990. Maintenance of B-cell memory by long-lived cells generated from proliferating precursors. Nature (Lond.). 346:749-751.
33. Kyburz, D., P. Aichele, D.E. Speiser, H. Hengartner, R. Zinkernagel, and H. Pircher. 1993. T cell immunity after a viral infection versus T cell tolerance induced by soluble viral peptides. Eur. J. Immunol. 23:1956-1962.
34. Battegay, M., S. Cooper, A. Althage, J. Baenziger, H. Hengartner, and R.M. Zinkemagel. 1991. Quantification of lymphocytic choriomeningitis virus with an immunological focus assay in 24 or 96 well plates. J. Virol. Methods. 33:191-198.
35. Monaco, A.P., M.L. Wood, and P.S. Russel. 1966. Studies on heterologous anti-lymphocyte serum in mice. III. Immunologic tolerance and chimensm across H-2 locus with adult thymectomy and anti-lymphocyte serum. Ann. NY Acad. Sci. 129:190-195.
36. Zinkernagel, R.M., T.P. Leist, H. Hengartner, and A. Althage. 1985. Susceptibility to lymphocytic choriomeningitis virus isolates correlates directly with early and high cytotoxic T cell activity, as well as with footpad swelling reaction, and all three are regulated by H-2D. J. Exp. Med. 162:2125-2141.
37. Sanders, M.E., M.W. Makgoba, and S. Shaw. 1988. Human naive and memory T cells: reinterpretation of helper-inducer and suppressor-inducer subsets. Immunol. Today. 9:195-199.
38. Kearney, E.R., K.A. Pape, D.Y. Loh, and M.K. Jenkins. 1994. Visualization of peptide-specific T cell immunity and peripheral tolerance induction in vivo. Immunity. 1:327-339.
39. McHcyzer-Williams, M.G., and M.M Davis 1995. Antigenspecific development of primary and memory T cells in vivo. Science (Wash. DC). 268:106-111.
40. + memory T cells. J. Immunol. 154:5870-5875.
41. Razvi, E.S., R.M. Welsh, and H.I. McFarland. 1995. In vivo state of antiviral CTL precursors. Characterization of a cycling cell population containing CTL precursors in immune mice. J. Immunol. 154:620-632.
42. Springer, T.A. 1990. Adhesion receptors of the immune system. Nature (Lond.). 346:425-433.
43. Hynes, R.O. 1992. Integrins: versatility, modulation, and signaling in cell adhesion. Cell. 69:11-25.
44. Baron, J.L., J.A. Madri, N.H. Ruddle, G. Hashim, and C.A.J. Janeway. 1995. Surface expression of α4 integrin by CD4 T cells is required for their entry into brain parenchyma. J. Exp. Med. 177:57-68.
45. + T cells to sites of infection. J. Immunol. 154:5293-5301.
46. + cytotoxic T cell activation and memory in virus infection. J. Immunol. 149:1326-1333.
47. Bradley, L.M., M. Croft, and S.L. Swain. 1993. T-cell memory: new perspectives. Immunol. Today. 14:197-199.
48. 51Cr-labelled mouse lymph node cells by treatment with lectins in intact and splenectomized hosts. Eur. J. Immunol. 5:831-838.