Modeling HLA associations with EBV-positive and -negative Hodgkin lymphoma suggests distinct mechanisms in disease pathogenesis

作者：Johnson Paul C D; McAulay Karen A; Montgomery Dorothy; Lake Annette; Shield Lesley; Gallagher Alice; Little Ann Margaret; Shah Anila; Marsh Steven G E; Taylor G Malcolm; Jarrett Ruth F^*

来源：International Journal of Cancer, 2015, 137(5): 1066-1075.

DOI：10.1002/ijc.29467

• Hodgkin lymphoma
• EBV
• HLA

HLA genotyping and genome wide association studies provide strong evidence for associations between Human Leukocyte Antigen (HLA) alleles and classical Hodgkin lymphoma (cHL). Analysis of these associations is complicated by the extensive linkage disequilibrium within the major histocompatibility region and recent data suggesting that associations with EBV-positive and EBV-negative cHL are largely distinct. To distinguish independent and therefore potentially causal associations from associations confounded by linkage disequilibrium, we applied a variable selection regression modeling procedure to directly typed HLA class I and II genes and selected SNPs from EBV-stratified patient subgroups. In final models, HLA-A*01:01 and B*37:01 were associated with an increased risk of EBV-positive cHL whereas DRB1*15:01 and DPB1*01:01 were associated with decreased risk. Effects were independent of a prior history of infectious mononucleosis. For EBV-negative cHL the class II SNP rs6903608 remained the strongest predictor of disease risk after adjusting for the effects of common HLA alleles. Associations with all cHL and differences by case EBV status reflected the subgroup analysis. In conclusion, this study extends previous findings by identifying novel HLA associations with EBV-stratified subgroups of cHL, highlighting those alleles likely to be biologically relevant and strengthening evidence implicating genetic variation associated with the SNP rs6903608.
What's new? Strong evidence exists for associations between HLA alleles and classical Hodgkin lymphoma (cHL). Analysis is however complicated by the linkage disequilibrium within the MHC region and data suggesting that associations with Epstein-Barr virus (EBV)-positive and negative cHL are distinct. In the largest study to date to investigate associations between EBV-stratified cHL subgroups and directly typed HLA alleles, the authors extend associations with EBV-positive cHL to novel HLA class II alleles, which are associated with decreased disease risk. For EBV-negative disease, the class II SNP rs6903608 remains the strongest predictor of risk after adjusting for the effects of common HLA alleles.

• 出版日期2015-9-1