CD8 T cells proliferate and differentiate into cytokine-secreting cytolytic effectors on encounter with viral antigens. As virus is cleared the activated T cells undergo apoptosis, but some survive and enter the memory pool where they persist indefinitely, slowly dividing in a relatively quiescent state until reactivation on reexposure to the antigen 1. The dynamics of this whole process can be variable and change as a consequence of the antigen load, the diversity of the available T cell repertoire, and the age of the host. During persistent infections, T cells and antigen coexist in an interactive environment, leading to a continued evolution of T cells that often become dysfunctional. New technologies with avidin-linked MHC tetramers, chimeric IgG–MHC dimers, and peptide-induced intracellular cytokine assays have allowed for the identification of multiclonal populations of antigen-specific T cells and are now showing...
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5 March 2001
Commentary|
March 05 2001
Assessing Cd8 T Cell Number and Dysfunction in the Presence of Antigen
Raymond M. Welsh
Raymond M. Welsh
aDepartment of Pathology, University of Massachusetts Medical School, Worcester, Massachusetts 01655
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Raymond M. Welsh
aDepartment of Pathology, University of Massachusetts Medical School, Worcester, Massachusetts 01655
Received:
January 26 2001
Accepted:
February 05 2001
Online ISSN: 1540-9538
Print ISSN: 0022-1007
© 2001 The Rockefeller University Press
2001
The Rockefeller University Press
J Exp Med (2001) 193 (5): F19–F22.
Article history
Received:
January 26 2001
Accepted:
February 05 2001
Citation
Raymond M. Welsh; Assessing Cd8 T Cell Number and Dysfunction in the Presence of Antigen. J Exp Med 5 March 2001; 193 (5): F19–F22. doi: https://doi.org/10.1084/jem.193.5.F19
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