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Specific Human Leukocyte Antigen Class I and II Alleles Associated with Hepatitis C Virus Viremia

  1. Author:
    Kuniholm, M. H.
    Kovacs, A.
    Gao, X. J.
    Xue, X. N.
    Marti, D.
    Thio, C. L.
    Peters, M. G.
    Terrault, N. A.
    Greenblatt, R. M.
    Goedert, J. J.
    Cohen, M. H.
    Minkoff, H.
    Gange, S. J.
    Anastos, K.
    Fazzari, M.
    Harris, T. G.
    Young, M. A.
    Strickler, H. D.
    Carrington, M.
  2. Author Address

    [Kuniholm, Mark H.; Xue, Xiaonan; Anastos, Kathryn; Fazzari, Melissa; Harris, Tiffany G.; Strickler, Howard D.] Albert Einstein Coll Med, Dept Epidemiol & Populat Hlth, Bronx, NY 10461 USA. [Kovacs, Andrea] Univ So Calif, Dept Pediat, Los Angeles, CA 90089 USA. [Gao, Xiaojiang; Marti, Darlene; Carrington, Mary] SAIC Frederick Inc, Natl Canc Inst Frederick, Expt Immunol Lab, Canc & Inflammat Program, Frederick, MD USA. [Thio, Chloe L.] Johns Hopkins Sch Med, Dept Med, Baltimore, MD USA. [Peters, Marion G.; Terrault, Norah A.] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA. [Greenblatt, Ruth M.] Univ Calif San Francisco, Dept Clin Pharm, San Francisco, CA 94143 USA. [Goedert, James J.] NCI, Div Canc Epidemiol & Genet, NIH, Rockville, MD USA. [Cohen, Mardge H.] Cook Cty Bur Hlth Serv, CORE Ctr, Chicago, IL USA. [Minkoff, Howard] Maimonides Hosp, Dept Obstet & Gynecol, Brooklyn, NY 11219 USA. [Gange, Stephen J.] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA. [Young, Mary A.] Georgetown Univ, Med Ctr, Dept Med, Washington, DC 20007 USA. [Carrington, Mary] Massachusetts Inst Technol & Harvard, Massachusetts Gen Hosp, Ragon Inst, Charlestown, MA USA.;Kuniholm, MH, Albert Einstein Coll Med, Dept Epidemiol & Populat Hlth, 1300 Morris Pk Ave,Belfer Bldg 1308, Bronx, NY 10461 USA.;mark.kuniholm@einstein.yu.edu
    1. Year: 2010
    2. Date: May
  1. Journal: Hepatology
    1. 51
    2. 5
    3. Pages: 1514-1522
  2. Type of Article: Article
  3. ISSN: 0270-9139
  1. Abstract:

    Studies of human leukocyte antigen (HLA) alleles and their relation with hepatitis C virus (HCV) viremia have had conflicting results. However, these studies have varied in size and methods, and few large studies assessed HLA class I alleles. Only one study conducted high-resolution class I genotyping. The current investigation therefore involved high-resolution HLA class I and II genotyping of a large multiracial cohort of U.S. women with a high prevalence of HCV and HIV. Our primary analyses evaluated associations between 12 HLA alleles identified through a critical review of the literature and HCV viremia in 758 HCV-seropositive women. Other alleles with >5% prevalence were also assessed; previously unreported associations were corrected for multiple comparisons. DRB1*0101 (prevalence ratio [PR] = 1.7; 95% confidence interval [CI] = 1.1-2.6), B*5701 (PR=2.0; 95% CI = 1.0-3.1), B*5703 (PR = 1.7; 95% CI = 1.0-2.5), and Cw*0102 (PR = 1.9; 95% CI = 1.0-3.0) were associated with the absence of HCV RNA (i.e., HCV clearance), whereas DRB1*0301 (PR = 0.4; 95% CI = 0.2-0.7) was associated with HCV RNA positivity. DQB1*0301 was also associated with the absence of HCV RNA but only among HIV-seronegative women (PR = 3.4; 95% CI = 1.2-11.8). Each of these associations was among those predicted. We additionally studied the relation of HLA alleles with HCV infection (serostatus) in women at high risk of HCV from injection drug use (N = 838), but no significant relationships were observed. Conclusion: HLA genotype influences the host capacity to clear HCV viremia. The specific HLA associations observed in the current study are unlikely to be due to chance because they were a priori hypothesized. (HEPATOLOGY 2010;51: 1514-1522.)

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External Sources

  1. DOI: 10.1002/hep.23515
  2. WOS: 000277261400008

Library Notes

  1. Fiscal Year: FY2009-2010
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