Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2023
IFNL4 Genotypes and Risk of Childhood Burkitt Lymphoma in East Africa.
СтатьяResearch Support, N.I.H., IntramuralПоддержка NIH: внешняя программаНазвание и аннотация: Перевод в очереди
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Baker Francine S, Wang Jeanny, Florez-Vargas Oscar, Brand Nathan R, Ogwang Martin D, Kerchan Patrick, Reynolds Steven J, Tenge Constance N, Were Pamela A, Kuremu Robert T, Wekesa Walter N, Masalu Nestory, Kawira Esther, Kinyera Tobias, Otim Isaac, Legason Ismail D, Nabalende Hadijah, Chagaluka George, Mutalima Nora, Borgstein Eric, Liomba George N, Kamiza Steve, Mkandawire Nyengo, Mitambo Collins, Molyneux Elizabeth M, Newton Robert, Prokunina-Olsson Ludmila, Mbulaiteye Sam M
Аннотация
Interferon lambda 4 (IFN-λ4) is a novel type-III interferon that can be expressed only by carriers of the genetic variant rs368234815-dG within the first exon of the IFNL4 gene. Genetic inability to produce IFN-λ4 (in carriers of the rs368234815-TT/TT genotype) has been associated with improved clearance of hepatitis C virus (HCV) infection. The IFN-λ4-expressing rs368234815-dG allele (IFNL4-dG) is most common (up to 78%) in West sub-Saharan Africa (SSA), compared to 35% of Europeans and 5% of individuals from East Asia. The negative selection of IFNL4-dG outside Africa suggests that its retention in African populations could provide survival benefits, most likely in children. To explore this hypothesis, we conducted a comprehensive association analysis between IFNL4 genotypes and the risk of childhood Burkitt lymphoma (BL), a lethal infection-associated cancer most common in SSA. We used genetic, epidemiologic, and clinical data for 4,038 children from the Epidemiology of Burkitt Lymphoma in East African Children and Minors (EMBLEM) and the Malawi Infections and Childhood Cancer case-control studies. Generalized linear mixed models fit with the logit link controlling for age, sex, country, P. falciparum infection status, population stratification, and relatedness found no significant association between BL risk and 3 coding genetic variants within IFNL4 (rs368234815, rs117648444, and rs142981501) and their combinations. Because BL occurs in children 6-9 years of age who survived early childhood infections, our results suggest that additional studies should explore the associations of IFNL4-dG allele in younger children. This comprehensive study represents an important baseline in defining the health effects of IFN-λ4 in African populations.