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The HLA-E-R/HLA-E-R Genotype Affects the Natural Course of Hepatitis C Virus (HCV) Infection and Is Associated with HLA-E-Restricted Recognition of an HCV-Derived Peptide by Interferon-gamma-Secreting Human CD8(+) T Cells

  作者 Schulte, D; Vogel, M; Langhans, B; Kramer, B; Korner, C; Nischalke, HD; Steinberg, V; Michalk, M; Berg, T; Rockstroh, JK; Sauerbruch, T; Spengler, U; Nattermann, J  
  选自 期刊  Journal of Infectious Diseases;  卷期  2009年200-9;  页码  1397-1401  
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[摘要]Recently, we showed chronic hepatitis C to be associated with increased expression of HLA-E and identified peptide hepatitis C virus (HCV) core amino acids 35-44 as a ligand for HLA-E that stabilizes HLA-E expression, favoring inhibition of natural killer cell cytotoxicity. Here we describe HLA-E-restricted recognition of peptide HCV core amino acids 35-44 by CD8(+) T cells. Frequency of HLA-E-restricted responses was significantly higher in patients homozygous for the HLA-E-R allele (60% vs 38%; P = .038). Moreover, we found that the HLA-E-R allelic variant confers protection against chronic infection with HCV genotypes 2 and 3. Taken together, our data indicate an important immunomodulating function of HLA-E in hepatitis C.

 
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