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The Journal of Immunology, 2005, 175: 5998-6005.
Copyright © 2005 by The American Association of Immunologists

Distinct Regulation of H2-M3-Restricted Memory T Cell Responses in Lymph Node and Spleen1

Alexander Ploss*,{dagger}, Ingrid Leiner* and Eric G. Pamer2,*

* Infectious Diseases Service, Department of Medicine and Laboratory of Antimicrobial Immunity, Immunology Program, Sloan-Kettering Institute, Memorial Sloan-Kettering Cancer Center, New York, NY 10021; and {dagger} Weill Graduate School of Medical Sciences of Cornell University, Immunology Program, New York, NY 10021

CD8 T cell populations restricted by H2-M3 MHC class Ib molecules expand rapidly during primary Listeria monocytogenes infection but only minimally upon reinfection. In contrast, CD8 T cells restricted by MHC class Ia molecules undergo more delayed expansion during primary infection but rapid and robust expansion following reinfection. In this study we demonstrate that primary H2-M3-restricted CD8 T cell responses are unaffected by the frequency of naive MHC class Ia-restricted T cells during L. monocytogenes infection. The magnitude of H2-M3-restricted memory responses, in contrast, is down-modulated by increasing frequencies of MHC class Ia-restricted effector T cells following secondary systemic infection. Suppression by MHC class Ia-restricted T cells, however, is not a universal feature of MHC class Ib-restricted memory responses. Primary systemic L. monocytogenes infection followed by secondary tissue infection, for example, results in robust expansion of H2-M3-restricted memory T cells in draining lymph nodes, despite the activation of MHC class Ia-restricted memory T cell responses. Thus, whereas MHC class Ia-restricted memory T cell populations predominate in spleens following systemic reinfection, H2-M3-restricted memory T cell responses remain prominent in lymph nodes draining localized infections. Our studies demonstrate that interactions between CD8 T cell populations can differ, depending on the status of the responding T cells (naive vs memory) and the route of reinfection. These results may have important implications for prime-boost vaccination strategies.




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M. T. Chow, S. Dhanji, J. Cross, P. Johnson, and H.-S. Teh
H2-M3-Restricted T Cells Participate in the Priming of Antigen-Specific CD4+ T Cells
J. Immunol., October 15, 2006; 177(8): 5098 - 5104.
[Abstract] [Full Text] [PDF]




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