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JCI table of contents, 2 April 2004

c cells

AUTHOR CONTACT:
Igor Belyakov
National Cancer Institute NIH, Bethesda, Maryland, USA.
Phone: 301-435-8341
Fax: 301-402-0549
E-mail: belyakov@mail.nih.gov

View the PDF of this article at: https://www.the-jci.org/press/20261.pdf


T Cell Balancing Act in Hepatitus C Chronic Infection

One of the main puzzles of hepatitis C viral (HCV) infection relates to how HCV can establish a persistent infection in the presence of a large number of T cells that are specific to HCV antigens, and should therefore result in HCV clearance from the organism's system. Upon HCV infection, HCV-specific CD8+ T-cells are massively recruited to the liver, but these cells have been shown to be inefficient in their activity against HCV infected cells. Now, Vincenzo Barbaba and colleagues of Universita degli Studi di Roma present the first data concerning the underlying reason for the inefficient activity of these T cells. Analyzing chronic HCV patients, the researchers found that the number of CD8+ regulatory T-cells (CD8+ Treg) was likewise increased. These CD8+ Treg cells produced large amounts of interleukin-10 (IL-10). Application of inhibitors to IL-10 restored CD8+ T-cell activity. This work marks the pivotal role that these regulatory T-cells play in controlling hepatic CD8+ T cell action during HCV infection and that the concomitant appearance off these two cell types may be the main factor in the establishment of chronic infection.

TITLE: Hepatic expansion of a virus-specific regulatory CD8+ T cell population in chronic hepatitis C virus infection

AUTHOR CONTACT:
Vincenzo Barnaba
Universita degli Studi di Roma, Rome, Italy.
Phone: 39-06-445-3994
Fax: 39-06-4938-3333
E-mail: vincenzo.barnaba@uniroma1.it
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Contact: Laurie Goodman
lgoodman@the-jci.org
212-342-4159
Journal of Clinical Investigation
2-Apr-2004


Page: 1 2 3 4 5 6 7 8 9 10 11 12 13

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