| Literature DB >> 32072624 |
Samuel Kirimunda1, Murielle Verboom2, Isaac Otim3, Mark Ssennono3,4, Ismail D Legason4, Hadijah Nabalende3, Martin D Ogwang3, Patrick Kerchan4, Tobias Kinyera3, Ivan Mwebaza1, Moses Joloba1, Leona W Ayers5, Steven J Reynolds6, Kishor Bhatia7, Olusegun O Onabajo8, Michael Hallensleben2, Robert J Biggar7, Ludmila Prokunina-Olsson8, James J Goedert7, Rainer Blasczyk2, Sam M Mbulaiteye7.
Abstract
Endemic Burkitt lymphoma (eBL) is an aggressive childhood B-cell lymphoma associated with Plasmodium falciparum (Pf) malaria and Epstein-Barr virus (EBV) infections. Variation in the Human Leukocyte Antigen (HLA) system is suspected to play a role, but assessments using less accurate serology-based HLA typing techniques in small studies yielded conflicting results. We studied 200 eBL cases and 400 controls aged 0-15 years enrolled in northern Uganda and typed by accurate high-resolution HLA sequencing methods. HLA results were analyzed at one- or two-field resolution. Odds ratios and 95% confidence intervals (aOR, 95% CI) for eBL risk associated with common HLA alleles versus alleles that were rare (<1%) or differed by <2% between the cases and controls as the reference category, were estimated using multiple logistic regression adjusting for age, sex, microgeography, region, malaria positivity and treatment history, and genetic variants associated with eBL. Compared to the controls, eBL cases had a lower frequency of HLA-A*02 (aOR = 0·59, 95% CI 0·38-0·91), HLA-B*41 (aOR = 0·36, 95% CI 0·13-1·00), and HLA-B*58 alleles (aOR = 0·59, 95% CI 0·36-0·97). eBL cases had a lower frequency of HLA-DPB1 homozygosity (aOR = 0·57, 95% CI 0·40-0·82) but a higher frequency of HLA-DQA1 homozygosity (aOR = 2·19, 95% CI 1·42-3·37). Our results suggest that variation in HLA may be associated with eBL risk.Entities:
Keywords: Burkitt lymphoma; Epstein-Barr virus; Plasmodium falciparum malaria; epidemiology; human leukocyte antigen; non-Hodgkin lymphoma
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Year: 2020 PMID: 32072624 PMCID: PMC7192769 DOI: 10.1111/bjh.16398
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 8.615