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HLA-Cw*04 and hepatitis C virus persistence

  1. Author:
    Thio, C. L.
    Gao, X. J.
    Goedert, J. J.
    Vlahov, D.
    Nelson, K. E.
    Hilgartner, M. W.
    O'Brien, S. J.
    Karacki, P.
    Astemborski, J.
    Carrington, M.
    Thomas, D. L.
  2. Author Address

    Johns Hopkins Univ, Dept Med, 424 N Bond St, Baltimore, MD 21231 USA Johns Hopkins Med Inst, Dept Med, Baltimore, MD 21205 USA Johns Hopkins Med Inst, Dept Epidemiol, Baltimore, MD 21205 USA NCI, Lab Genom Divers, Frederick, MD 21701 USA NCI, Div Canc Epidemiol & Genet, Viral Epidemiol Branch, Rockville, MD USA Cornell Med Ctr, New York Presbyterian Hosp, Dept Pediat, New York, NY USA New York Acad Med, New York, NY USA Thio CL Johns Hopkins Univ, Dept Med, 424 N Bond St, Baltimore, MD 21231 USA
    1. Year: 2002
  1. Journal: Journal of Virology
    1. 76
    2. 10
    3. Pages: 4792-4797
  2. Type of Article: Article
  1. Abstract:

    In studies of acute hepatitis C virus (HCV) infection, the early host immune response is one of the determinants of viral persistence. The class I human leukocyte antigens (HLA), which present foreign antigen to cytolytic T cells, are integral components of this response. We hypothesized that the highly polymorphic HLA genes affect the outcome of an HCV infection. To test this hypothesis, we molecularly typed 231 persons with well-documented clearance of an HCV infection and 444 matched persistently infected persons. HLA-A*1101 (odds ratio [OR], 0.49; 95% confidence interval [95% CI], 0.27 to 0.89), HLA-B*57 (OR, 0.62; 95% Cl, 0.39 to 1.00), and HLA-Cw*0102 (OR, 0.43; 95% CI, 0.21 to 0.89) were associated with viral clearance, whereas HLA-A*2301 (OF, 1.78; 95% CI, 1.01 to 3.11) and HLA- Cw*04 (OR, 1.78; 95% CI, 1.21 to 2.59) were associated with viral persistence. HLA-Cw*04 is in strong linkage disequilibrium with HLA-B*53 and HLA-B*35, but only HLA-B*53 (OR, 1.70, 95% CI, 0.95 to 3.06) and the Cw*04-B*53 haplotype (OR, 1.76; 95% CI, 0.94 to 3.26) were weakly associated with viral persistence. HLA-B*53 has similar, but not necessarily identical, binding specificity to some HLA-B*35 subtypes (B*35- Px group). The association with the B*35-Px group was less strong than with HLA-B*53 alone. The association of HLA-Cw*04 with HCV persistence was codominant (two copies of the gene were more strongly associated with persistence than one copy). However, HLA*04 was not associated with HCV RNA levels among the persistently infected individuals. Since Cw*04 is a ligand for the killer immunoglobulin-like receptors on natural killer cells, these cells may be involved in recovery from HCV infection. Further investigation is needed to understand the relationship between class I alleles and HCV clearance.

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