Distinct MHC class I and II alleles are associated with hepatitis C viral clearance, originating from a single source

被引:206
作者
McKiernan, SM [1 ]
Hagan, R
Curry, M
McDonald, GSA
Kelly, A
Nolan, N
Walsh, A
Hegarty, J
Lawlor, E
Kelleher, D
机构
[1] St James Hosp, Hepatol Ctr, Dublin 8, Ireland
[2] Trinity Coll Dublin, Dept Community Hlth & Gen Practice, Dublin, Ireland
[3] Irish Blood Transfus Serv, Dublin, Ireland
[4] St Vincents Hosp, Dublin 4, Ireland
[5] St James Hosp, Dept Microbiol, Dublin, Ireland
关键词
D O I
10.1002/hep.20261
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The role of cytotoxic T lymphocyte responses, restricted by human leukocyte antigen (HLA) class I alleles, is recognized as highly significant in the successful clearance of hepatitis C virus (HCV). The frequency of class I alleles in females inoculated with HCV genotype 16 from a single source was examined for an association with outcome. Class I typing was performed using polymerase chain reaction sequence-specific primers in 227 female subjects: 141 had chronic infection and 86 had viral clearance. Statistical analysis included chi(2) testing and multiple logistic regression analysis. A*03, B*27, and Cw*01 occurred more frequently in those with viral clearance (39.5%, 14%, and 9.3%, respectively) compared with those with chronic infection (19.1%, 2.1%, and 1.4%, respectively; P less than or equal to .005). B*08 occurred more often in those with chronic infection compared with viral clearance (39.7% vs. 19.8%; P = .002). In combination with previously reported class II allele associations, over 75% that successfully eliminate HCV carry either A*03, DRB1*0101, or *0401, compared with only 37% of those with chronic infection (P < .0001). The haplotypes A*03-B*07-DRB1*15-DQB1*0602 and A*02-B*27-Cw*01-DRB1*0101-DQB1*0501 are associated with viral clearance (P = .004 and .01, respectively). By multiple logistic regression analysis, the alleles A*03, B*27, DRB1*0101, *0401, and *15 are associated with viral clearance, and B*27 has the strongest association (odds ratio [OR] 7.99). The haplotype A*01-B*08-Cw*07-DRB1*03011-DQB1*0201 is associated with chronic infection (P = .002), being independent for DQB1*0201 (OR 0.27). In conclusion, certain class I alleles are associated with outcome in this homogenous cohort. More significantly, either HLA-A*03, -DRB1*0101, or -*0401 are carried by an overwhelming majority of those subjects who successfully clear HCV.
引用
收藏
页码:108 / 114
页数:7
相关论文
共 36 条
[1]   THE NATURAL-HISTORY OF COMMUNITY-ACQUIRED HEPATITIS-C IN THE UNITED-STATES [J].
ALTER, MJ ;
MARGOLIS, HS ;
KRAWCZYNSKI, K ;
JUDSON, FN ;
MARES, A ;
ALEXANDER, WJ ;
HU, PY ;
MILLER, JK ;
GERBER, MA ;
SAMPLINER, RE ;
MEEKS, EL ;
BEACH, MJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 327 (27) :1899-1905
[2]   EPIDEMIOLOGY OF HEPATITIS-C IN THE WEST [J].
ALTER, MJ .
SEMINARS IN LIVER DISEASE, 1995, 15 (01) :5-14
[3]  
[Anonymous], MODERN EPIDEMIOLOGY
[4]   HEPATITIS-C VIRUS (HCV) GENOTYPE, TISSUE HCV ANTIGENS, HEPATOCELLULAR EXPRESSION OF HLA-A,B,C, AND INTERCELLULAR ADHESION-1 MOLECULES - CLUES TO PATHOGENESIS OF HEPATOCELLULAR DAMAGE AND RESPONSE TO INTERFERON TREATMENT IN PATIENTS WITH CHRONIC HEPATITIS-C [J].
BALLARDINI, G ;
GROFF, P ;
PONTISSO, P ;
GIOSTRA, F ;
FRANCESCONI, R ;
LENZI, M ;
ZAULI, D ;
ALBERTI, A ;
BIANCHI, FB .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (05) :2067-2075
[5]   Phototyping: Comprehensive DNA typing for HLA-A, B, C, DRB1, DRB3, DRB4, DRB5 & DQB1 by PCR with 144 primer mixes utilizing sequence-specific primers (PCR-SSP) [J].
Bunce, M ;
ONeill, CM ;
Barnardo, MCNM ;
Krausa, P ;
Browning, MJ ;
Morris, PJ ;
Welsh, KI .
TISSUE ANTIGENS, 1995, 46 (05) :355-367
[6]  
Chang KM, 1999, J IMMUNOL, V162, P1156
[7]   Analysis of a successful immune response against hepatitis C virus [J].
Cooper, S ;
Erickson, AL ;
Adams, EJ ;
Kansopon, J ;
Weiner, AJ ;
Chien, DY ;
Houghton, M ;
Parham, P ;
Walker, CM .
IMMUNITY, 1999, 10 (04) :439-449
[8]   Comparative rates of nucleotide sequence variation in the hypervariable region of E1/E2 and the NS5b region of hepatitis C virus in patients with a spectrum of liver disease resulting from a common source of infection [J].
Duffy, M ;
Salemi, M ;
Sheehy, N ;
Vandamme, AM ;
Hegarty, J ;
Curry, M ;
Nolan, N ;
Kelleher, D ;
McKiernan, S ;
Hall, WW .
VIROLOGY, 2002, 301 (02) :354-364
[9]   Association of hepatitis C virus-specific CD8+ T cells with viral clearance in acute hepatitis C [J].
Grüner, NH ;
Gerlach, TJ ;
Jung, MC ;
Diepolder, HM ;
Schirren, CA ;
Schraut, WW ;
Hoffmann, R ;
Zachoval, R ;
Santantonio, T ;
Cucchiarini, M ;
Cerny, A ;
Pape, GR .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (05) :1528-1536
[10]   Quantitative analysis of hepatitis C virus-specific CD8+ T cells in peripheral blood and liver using peptide-MHC tetramers [J].
He, XS ;
Rehermann, B ;
López-Labrador, FX ;
Boisvert, J ;
Cheung, R ;
Mumm, J ;
Wedemeyer, H ;
Berenguer, M ;
Wright, TL ;
Davis, MM ;
Greenberg, HB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (10) :5692-5697