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Recognition of a novel naturally processed, A2 restricted, HCV-NS4 epitope triggers IFN-gamma release in absence of detectable cytopathicity
Authors:Jeff Alexander  Marie-France Del Guercio  John D Fikes  Robert W Chesnut  Francis V Chisari  Kyong-Mi Chang  Ettore Appella  Alessandro Sette
Institution:

a Epimmune Inc., 6555 Nancy Ridge Drive, Suite 200, San Diego, CA 92121, USA (J.A., M-F.D.G., J.D.F., R.W.C., A.S.)

b The Scripps Research Institute, Department of Molecular and Experimental Medicine, 10666 Torrey Pines Road, La Jolla, CA 92037, USA (F.V.C., K.C.)

c National Cancer Institute, Laboratory of Cell Biology, Building 37, Room 1B04, 37 Convent Drive MSC 4255, Bethesda, MD 20892, USA (E.A.)

Abstract:Using short term CTL lines derived from HLA A2/Kb transgenic mice and IFN-gamma release assays we demonstrate that the NS4.1769 epitope, is generated from natural processing of the NS4 antigen, and presented in the context of the A2/Kb molecules. Interestingly, T cell recognition of the naturally processed form of the NS4.1769 epitope was associated with significant IFN-gamma release, but no direct cytolytic activity. Epitopes of this phenotype might be of interest, in terms of therapy of chronic HCV infection by associating the benefit of localized lymphokine release with low or absent direct cytopathicity.
Keywords:Abbreviations: CTL  cytotoxic T lymphocytes  IFN-gamma  interferon gamma  NS4  nonstructural protein 4  HCV  hepatitis C virus  HBV  hepatitis B virus  TNF  tumor necrosis factor  HPLC  high performance liquid chromatography  s  c    subcutaneous  RSV  Rous sorcoma virus  PBS  phosphate-buffered saline  IFA  incomplete Freund’s adjuvant
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