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Dynamic programming of CD8+ T lymphocyte responses

Abstract

The initial encounter with an antigen-presenting cell (APC) is the primary force behind the expansion, differentiation and survival of naive T cells. Using an APC that permits temporal control of priming, we examined whether the duration of antigenic stimulation can influence the functional development of CD8+ cytotoxic T lymphocytes (CTLs) in vivo. Whereas CTLs given a 4-h stimulus underwent an abortive clonal expansion with transient surface CD25 expression, those given a 20-h stimulus sustained CD25 up-regulation, proliferated extensively, and efficiently mediated destruction of peripheral target tissues. Our results show that an instructional program preceding the first cell division integrates differences in signal strength into the decision to activate versus tolerize specific CTL clones.

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Figure 1: In vitro and in vivo expansion of OT-I CTLs.
Figure 2: Abortive expansion in vivo is not overcome by overexpression of Bcl-2 or Bcl-xL.
Figure 3: Sustained antigenic stimulation leads to increased IL-2 production and IL-2 receptor-α expression.
Figure 4: Briefly stimulated CTLs show decreased cytotoxicity in vivo.

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References

  1. Harty, J.T., Tvinnereim, A.R. & White, D.W. CD8+ T cell effector mechanisms in resistance to infection. Annu. Rev. Immunol. 18, 275–308 (2000).

    Article  CAS  PubMed  Google Scholar 

  2. Kaech, S.M., Wherry, E.J. & Ahmed, R. Effector and memory T-cell differentiation: implications for vaccine development. Nat. Rev. Immunol. 2, 251–262 (2002).

    Article  CAS  PubMed  Google Scholar 

  3. Murali-Krishna, K. et al. Counting antigen-specific CD8 T cells: a reevaluation of bystander activation during viral infection. Immunity 8, 177–187 (1998).

    Article  CAS  PubMed  Google Scholar 

  4. Butz, E.A. & Bevan, M.J. Massive expansion of antigen-specific CD8+ T cells during an acute virus infection. Immunity 8, 167–175 (1998).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Blattman, J.N. et al. Estimating the precursor frequency of naive antigen-specific CD8 T cells. J. Exp. Med. 195, 657–664 (2002).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Lanzavecchia, A. & Sallusto, F. Dynamics of T lymphocyte responses: intermediates, effectors, and memory cells. Science 290, 92–97 (2000).

    Article  CAS  PubMed  Google Scholar 

  7. Heath, W.R. & Carbone, F.R. Cross-presentation, dendritic cells, tolerance and immunity. Annu. Rev. Immunol. 19, 47–64 (2001).

    Article  CAS  PubMed  Google Scholar 

  8. Steinman, R.M. & Nussenzweig, M.C. Avoiding horror autotoxicus: the importance of dendritic cells in peripheral T cell tolerance. Proc. Natl. Acad. Sci. USA 99, 351–8 (2002).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Iezzi, G., Karjalainen, K. & Lanzavecchia, A. The duration of antigenic stimulation determines the fate of naive and effector T cells. Immunity 8, 89–95 (1998).

    Article  CAS  PubMed  Google Scholar 

  10. Iezzi, G., Scotet, E., Scheidegger, D. & Lanzavecchia, A. The interplay between the duration of TCR and cytokine signaling determines T cell polarization. Eur. J. Immunol. 29, 4092–4101 (1999).

    Article  CAS  PubMed  Google Scholar 

  11. van Stipdonk, M.J., Lemmens, E.E. & Schoenberger, S.P. Naive CTLs require a single brief period of antigenic stimulation for clonal expansion and differentiation. Nat. Immunol. 2, 423–429 (2001).

    Article  CAS  PubMed  Google Scholar 

  12. Kaech, S.M. & Ahmed, R. Memory CD8+ T cell differentiation: initial antigen encounter triggers a developmental program in naive cells. Nat. Immunol. 2, 415–422 (2001).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Wong, P. & Pamer, E. Antigen-independent CD8 T cell proliferation. J. Immunol. 166, 5864–5868 (2001).

    Article  CAS  PubMed  Google Scholar 

  14. Miller, M.J., Wei, S.H., Parker, I. & Cahalan, M.D. Two-photon imaging of lymphocyte motility and antigen response in intact lymph node. Science 296, 1869–1873 (2002).

    Article  CAS  PubMed  Google Scholar 

  15. Stoll, S., Delon, J., Brotz, T.M. & Germain, R.N. Dynamic imaging of T cell–dendritic cell interactions in lymph nodes. Science 296, 1873–1876 (2002).

    Article  PubMed  Google Scholar 

  16. Schoenberger, S.P. et al. Efficient direct priming of tumor-specific cytotoxic T lymphocyte in vivo by an engineered APC. Cancer Res. 58, 3094–3100 (1998).

    CAS  PubMed  Google Scholar 

  17. Hogquist, K.A. et al. T cell receptor antagonist peptides induce positive selection. Cell 76, 17–27 (1994).

    Article  CAS  PubMed  Google Scholar 

  18. Plas, D., Rathmell, J. & Thompson, C. Homeostatic control of lymphocyte survival: potential origins and implications. Nat. Immunol. 3, 515–521 (2002).

    Article  CAS  PubMed  Google Scholar 

  19. Chao, D. et al. Bcl-XL and Bcl-2 repress a common pathway of cell death. J Exp Med 182, 821–828 (1995).

    Article  CAS  PubMed  Google Scholar 

  20. Strasser, A., Harris, A. & Cory, S. bcl-2 transgene inhibits T cell death and perturbs thymic self-censorship. Cell 67, 889–899 (1991).

    Article  CAS  PubMed  Google Scholar 

  21. Dai, Z., Konieczny, B. & Lakkis, F. The dual role of IL-2 in the generation and maintenance of CD8+ memory T cells. J. Immunol. 165, 3031–3036 (2000).

    Article  CAS  PubMed  Google Scholar 

  22. Oehen, S. & Brduscha-Riem, K. Differentiation of naive CTL to effector and memory CTL: correlation of effector function with phenotype and cell division. J. Immunol. 161, 5338–5346 (1998).

    CAS  PubMed  Google Scholar 

  23. Kurts, C., Kosaka, H., Carbone, F.R., Miller, J.F. & Heath, W.R. Class I-restricted cross-presentation of exogenous self-antigens leads to deletion of autoreactive CD8+ T cells. J. Exp. Med. 186, 239–245 (1997).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Kurts, C. et al. CD4+ T cell help impairs CD8+ T cell deletion induced by cross- presentation of self-antigens and favors autoimmunity. J. Exp. Med. 186, 2057–2062 (1997).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Nelson, B. & Willerford, D. The biology of the interleukin-2 receptor. Adv. Immunol. 70, 1–81 (1998).

    Article  CAS  PubMed  Google Scholar 

  26. Liu, K. et al. Immune tolerance after delivery of dying cells to dendritic cells in situ. J. Exp. Med. 196, 1091–1097 (2002).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

This is manuscript no. 529 from the La Jolla Institute for Allergy and Immunology, La Jolla, CA. Supported by grants from the American Cancer Society, the National Institutes of Health, Cap CURE and the Netherlands Cancer Society.

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Correspondence to Stephen P. Schoenberger.

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van Stipdonk, M., Hardenberg, G., Bijker, M. et al. Dynamic programming of CD8+ T lymphocyte responses. Nat Immunol 4, 361–365 (2003). https://doi.org/10.1038/ni912

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