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Blood, 15 November 2006, Vol. 108, No. 10, pp. 3414-3419.
Prepublished online as a Blood First Edition Paper on August 1, 2006; DOI 10.1182/blood-2006-06-030668.


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Submitted January 27, 2006
Accepted July 6, 2006

Nef interference with HIV-1-specific CTL antiviral activity is epitope specific

Sama Adnan, Arumugam Balamurugan, Alicja Trocha, Michael S Bennett, Hwee L Ng, Ayub Ali, Christian Brander, and Otto O Yang*

University of California, Los Angeles, CA
Massachusetts General Hospital, Harvard University, Boston, MA

* Corresponding author; email: oyang{at}mednet.ucla.edu.

HIV-1 Nef and HIV-1-specific CTL have important and opposing roles in the immunopathogenesis of HIV-1 infection. Nef-mediated downmodulation of HLA class I on infected cells can confer resistance to CTL clearance, but the factors determining the efficiency of this process are unknown. This study examines the impact of Nef on the antiviral activity of several CTL clones recognizing epitopes from early and late HIV-1 proteins, restricted by HLA- A, B, and C molecules. CTL targeting epitopes in early proteins remained susceptible to the effects of Nef, although possibly to a lesser degree than CTL targeting late protein epitopes, indicating that significant Nef-mediated HLA downregulation can precede even the presentation of early protein-derived epitopes. However, HLA-C- restricted CTL were unaffected by Nef, consistent with downregulation of cell surface HLA- A and B but not C molecules. Thus CTL vary dramatically in their susceptibility to Nef interference, suggesting differences in the relative importance of HLA- A- and B- versus C-restricted CTL in vivo. The data thus indicate that C-restricted CTL may have an underappreciated antiviral role in the setting of Nef in vivo, and suggest a benefit of promoting C-restricted CTL for immunotherapy or vaccine development.


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