Association of HLA class I and II alleles and extended haplotypes with nasopharyngeal carcinoma in Taiwan

Allan Hildesheim*, Raymond J. Apple, Chien Jen Chen, Sophia S. Wang, Yu Juen Cheng, William Klitz, Steven J. Mack, I. How Chen, Mow Ming Hsu, Czau Siung Yang, Louise A. Brinton, Paul H. Levine, Henry A. Erlich

*此作品的通信作者

研究成果: 期刊稿件文章同行評審

195 引文 斯高帕斯(Scopus)

摘要

Background: Nasopharyngeal carcinoma (NPC), which occurs at a disproportionately high rate among Chinese individuals, is associated with Epstein-Barr virus (EBV). Human leukocyte antigen (HLA) polymorphisms appear to play a role in NPC, because they are essential in the immune response to viruses. We used high-resolution HLA genotyping in a case-control study in Taiwan to systematically evaluate the association between various HLA alleles and NPC. Methods: We matched 366 NPC case patients to 318 control subjects by age, sex, and geographic residence. Participants were interviewed and provided blood samples for genotyping. High-resolution (polymerase chain reaction-based) genotyping of HLA class I (A and B) and II (DRB1, DQA1, DQB1, and DPB1) genes was performed in two phases. In phase I, 210 case patients and 183 control subjects were completely genotyped. In phase II, alleles associated with NPC in the phase I analysis were evaluated in another 156 case patients and 135 control subjects. Extended haplotypes were inferred. Results: We found a consistent association between HLA-A*0207 (common among Chinese but not among Caucasians) and NPC (odds ratio [OR] =2.3, 95% confidence interval [CI] = 1.5 to 3.5) but not between HLA-A*0201 (most common HLA-A2 allele in Caucasians) and NPC (OR = 0.79, 95% CI = 0.55 to 1.2). Individuals with HLA-B*4601, which is in linkage disequilibrium with HLA-A*0207, had an increased risk for NPC (OR = 1.8, 95% CI = 1.2 to 2.5) as did individuals with HLA-A*0207 and HLA-B*4601 (OR = 2.8, 95 % CI = 1.7 to 4.4). Individuals homozygous for HLA-A*1101 had decreased risks for NPC (OR = 0.24, 95% CI = 0.13 to 0.46). The extended haplotype this ethnic group, was associated with a statistically significantly increased risk for NPC (OR = 2.6, 95 % CI = 1.1 to 6.4). Conclusions: The restriction of the association of HLA-A2 with NPC to HLA-A*0207 probably explains previously observed associations of HLA-A2 with NPC among Chinese but not Caucasians. The extended haplotypes associated with NPC might, in part, explain the higher rates of NPC in this ethnic group.

原文英語
頁(從 - 到)1780-1789
頁數10
期刊Journal of the National Cancer Institute
94
發行號23
DOIs
出版狀態已出版 - 04 12 2002
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