4.6 Article

HLA-Cw*04 and hepatitis C virus persistence

Journal

JOURNAL OF VIROLOGY
Volume 76, Issue 10, Pages 4792-4797

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.76.10.4792-4797.2002

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Funding

  1. NCI NIH HHS [N01-CP-33002, N01-CO-56000] Funding Source: Medline
  2. NCRR NIH HHS [M01 RR000071, M01-RR02558, M01-RR06020, M01 RR002558, M01-RR00071, M01 RR000059, M01-RR00059] Funding Source: Medline
  3. NICHD NIH HHS [N01-HD-4-3200] Funding Source: Medline
  4. NIDA NIH HHS [R37 DA004334, DA00441, DA04334, DA13324, R56 DA004334, R01 DA013324, R01 DA004334, K08 DA000441] Funding Source: Medline
  5. PHS HHS [MCJ-060570] Funding Source: Medline

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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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