Associations between the human MHC and sustained virologic response in the treatment of chronic hepatitis C virus infection

S. L. Rhodes, H. Erlich, K. A. Im, J. Wang, J. Li, T. Bugawan, L. Jeffers, X. Tong, X. Su, H. R. Rosen, L. J. Yee, T. J. Liang, H. Yang

Research output: Contribution to journalArticlepeer-review

21 Scopus citations


The human major histocompatability complex (MHC) genes encode the human leukocyte antigens, which are important in antigen presentation and regulation of CD8+ and CD4+ T cells. Response to therapies in hepatitis C virus (HCV) infection is highly variable (30-80%) and lower response rates have been reported among African Americans (AA; ∼30%) compared to Caucasian Americans (CA; ∼50%) infected with genotype-1 viruses. We evaluated whether MHC gene variants were associated with response to therapy and racial differences in AA and CA sustained virologic response (SVR) rates. We genotyped alleles at 8 MHC loci: 3 class I (A, B and C) and 5 class II (DRB1, DQA1, DQB1, DPA1 and DPB1) loci in 373 individuals (179 AA and 194 CA) with genotype-1 HCV infections, who were treated with peginterferon-α-2a and ribavirin. We observed carriage of A*02 (RR=1.33(1.08-1.64); P=0.008), B*58 (RR=1.84(1.24-2.73); P=0.002) and DPB1*1701 (RR=1.57(1.09-2.26); P=0.015) to be associated with SVR after adjustment for other predictors of response. In analysis of AA and CA subgroups separately, we observed potential, though not statistically significant, differences in these MHC associations. Variation in the immunogenetic background of HCV-infected individuals might account for some observed variation in viral-specific immunity and courses of disease. In this regard, future studies examining broader patient populations are warranted.

Original languageEnglish (US)
Pages (from-to)328-333
Number of pages6
JournalGenes and Immunity
Issue number4
StatePublished - Jun 2008
Externally publishedYes

ASJC Scopus subject areas

  • Genetics(clinical)
  • Immunology
  • Genetics


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