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Nature 439, 669-670 (9 February 2006) | doi:10.1038/439669a; Published online 8 February 2006
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Research Assistant Professor, Post-Doctoral Fellow, Statistical Genetic Analyst, and Scientific Programmer Positions in Statistical Human Genetics
- University of Michigan
- Ann Arbor, Michigan, USA
Faculty Positions in Cancer, Cardiovascular and Metabolic Diseases, Immunology
- Institut de recherches cliniques de Montreal
- Montreal, Quebec, Canada
Immunology: Exhausted T cells perk up
Matthew A. Williams1 & Michael J. Bevan1
Abstract
During persistent infections, the immune cells responsible for killing infected cells and maintaining inflammation gradually stop functioning, allowing the pathogen to thrive. But can this process be reversed?
There are many checks and balances in place to control the immune response to a pathogenic onslaught: too little of a reaction and the invader can kill the host or take up residence; too much and the immune system can itself start to damage tissues. On page 682 of this issue, Barber et al.1 demonstrate that a receptor–ligand pair involved in controlling the immune response can be blocked by antibodies to revive dysfunctional T cells and clear a chronic viral infection.
- Matthew A. Williams and Michael J. Bevan are in the Howard Hughes Medical Institute, and Department of Immunology, University of Washington, PO Box 357370, Seattle, Washington 98195-7370, USA.
Email: mbevan@u.washington.edu
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