Human leukocyte antigen class I and II alleles in non-Hodgkin lymphoma etiology

Author:

Wang Sophia S.1,Abdou Amr M.2,Morton Lindsay M.3,Thomas Rasmi2,Cerhan James R.4,Gao Xiaojiang2,Cozen Wendy5,Rothman Nathaniel3,Davis Scott6,Severson Richard K.7,Bernstein Leslie1,Hartge Patricia3,Carrington Mary28

Affiliation:

1. Division of Cancer Etiology, Department of Population Sciences, City of Hope, Duarte, CA;

2. Cancer and Inflammation Program, Laboratory of Experimental Immunology, SAIC-Frederick Inc, NCI-Frederick, MD;

3. Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD;

4. College of Medicine, Mayo Clinic, Rochester, MN;

5. Norris Comprehensive Cancer Center, University of Southern California, Los Angeles;

6. Fred Hutchinson Cancer Research Center and University of Washington, Seattle;

7. Department of Family Medicine and Public Health Sciences, Wayne State University and Karmanos Cancer Institute, Detroit, MI; and

8. Ragon Institute of the Massachusetts General Hospital, Massachusetts Institute of Technology and Harvard University, Boston

Abstract

Abstract Genome-wide association and candidate gene studies implicate different genetic variants within the 6p21 chromosomal region with different non-Hodgkin lymphoma (NHL) subtypes. Complementing these efforts, we conducted human leukocyte antigen (HLA) class I and class II genotyping among 610 NHL cases and 555 controls of non-Hispanic white descent from a US multicenter study. Allele-disease associations were assessed by logistic regression for NHL and its subtypes. Statistically significant associations between HLA and NHL subtypes include HLA-DRB1*0101 for follicular lymphoma (odds ratio [OR] = 2.14, P < .001), HLA-DRB1*0401 for diffuse large B-cell lymphoma (DLBCL; OR = 0.45, P = .006), and HLA-DRB1*13 and follicular lymphoma (OR = 0.48, P = .008). We further observed significant heterozygote advantage for HLA class I alleles and NHL, and particularly DLBCL (P trend = .01 for elevated risk with increasing number of homozygous alleles). Our results support a role for HLA in the etiology of NHL and its subtypes.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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