Comprehensive Analysis of Class I and Class II HLA Antigens and Chronic Hepatitis B Virus Infection

Author:

Thio Chloe L.1,Thomas David L.1,Karacki Peter1,Gao Xiaojiang2,Marti Darlene2,Kaslow Richard A.3,Goedert James J.4,Hilgartner Margaret5,Strathdee Steffanie A.6,Duggal Priya6,O'Brien Stephen J.2,Astemborski Jacquie1,Carrington Mary2

Affiliation:

1. Department of Medicine

2. Laboratory of Genomic Diversity, National Cancer Institute, Frederick

3. Department of Epidemiology, University of Alabama, Birmingham, Alabama

4. Viral Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland

5. Department of Pediatrics, New York Presbyterian Hospital-Cornell Medical Center, New York, New York

6. Department of Epidemiology, Johns Hopkins Medical Institutions, Baltimore

Abstract

ABSTRACT Following an acute hepatitis B virus (HBV) infection, clearance or persistence is determined in part by the vigor and breadth of the host immune response. Since the human leukocyte antigen system (HLA) is an integral component of the immune response, we hypothesized that the highly polymorphic HLA genes are key determinants of viral clearance. HLA class I and II genes were molecularly typed in 194 Caucasian individuals with viral persistence and 342 matched controls who had cleared the virus. A single class I allele, A*0301 (odds ratio [OR], 0.47; 95% confidence interval [CI], 0.30 to 0.72; P = 0.0005) was associated with viral clearance. The class II allele DRB1*1302 was also associated with clearance (OR, 0.42; 95% CI, 0.19 to 0.93; P = 0.03), but its significance decreased in a multivariate model that included other alleles associated with disease outcome as covariates. B*08 was associated with viral persistence both independently (OR, 1.59; 95% CI, 1.04 to 2.43; P = 0.03) and as part of the conserved Caucasian haplotype A*01-B*08-DRB1*03 . The B*44-Cw*1601 (OR, 2.23; 95% CI, 1.13 to 4.42; P = 0.02) and B*44-Cw*0501 (OR, 1.99; 95% CI, 1.22 to 3.24; P = 0.006) haplotypes were also associated with viral persistence. Interestingly, both the B*08 haplotype and DR7 , which forms a haplotype with B*44-Cw*1601 , have been associated with nonresponse to the HBV vaccine. The associations with class I alleles are consistent with a previously implicated role for CD8-mediated cytolytic-T-cell response in determining the outcome of an acute HBV infection.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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