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The Journal of Immunology, 2004, 173: 4084-4090.
Copyright © 2004 by The American Association of Immunologists

The Development of Functional CD8 T Cell Memory after Listeria monocytogenes Infection Is Not Dependent on CD401

Megan J. Montfort*, H. G. Archie Bouwer*,{ddagger},§, Cynthia R. Wagner{dagger},§ and David J. Hinrichs2,*,{ddagger},§

Departments of * Molecular Microbiology and Immunology and {dagger} Cardiology, Oregon Health and Science University, Portland, OR 97239; {ddagger} Earle A. Chiles Research Institute, Providence Portland Medical Center, Portland, OR 97213; and § Immunology Research, Veterans Affairs Medical Center, Portland, OR 97239

The immunologic requirements for generating long-lived protective CD8 T cell memory remain unclear. Memory CD8 populations generated in the absence of CD4 Th cells reportedly have functional defects, and at least a subset of CD8 T cells transiently express CD40 after activation, suggesting that direct CD4-CD8 T cell interactions through CD40 may influence the magnitude and functional quality of memory CD8 populations. To ascertain the role of CD40 in such direct T cell interactions, we investigated CD8 T cell responses in CD40–/– mice after infection with Listeria monocytogenes, an intracellular bacterium that induces APC activation and thus priming of CD8 T cells independently of CD4 Th cell help through CD40. In this study we show that memory CD8 T cells generated in CD40-deficient mice show in vivo cytotoxicity and cytokine production equivalent to CD8 memory T cells from wild-type mice. Upon secondary Listeria infection, CD40–/– memory CD8 T cells expand to greater numbers than seen in wild-type mice. These results indicate that CD40 ligation on CD8 T cells, although reportedly a part of CD8 T cell memory development in an H-Y-directed response, is not needed for the development of functional memory CD8 T cell populations after Listeria infection.




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