Distribution of HLA-A, -B, -C,-DRB1,-DQB1,-DPB1 allele frequencies in patients with COVID-19 bilateral pneumonia in Russians, living in the Chelyabinsk region (Russia)

被引:7
作者
Suslova, Tatiana A. [1 ]
Vavilov, Mikhail N. [1 ]
Belyaeva, Svetlana, V [1 ]
Evdokimov, Alexander, V [1 ]
Stashkevich, Daria S. [1 ]
Galkin, Alexander [2 ]
Kofiadi, Ilya A. [3 ]
机构
[1] Chelyabinsk State Univ, Chelyabinsk, Russia
[2] Weill Cornell Med, Feil Family Brain & Mind Res Inst, 407 East 61st St, New York, NY 10065 USA
[3] Pirogov Russian Natl Reseach Med Univ, Moscow, Russia
关键词
HLA; DPB1; rs9277534; COVID-19; NGS;
D O I
10.1016/j.humimm.2022.04.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In this population-based case-control study conducted in the Chelyabinsk region of Russia, we examined the distribution of HLA-A, -B, -C, -DRB1, -DQB1 and -DPB1, in a group of 100 patients with confirmed COVID-19 bilateral pneumonia. Typing was performed by NGS and statistical calculations were carried out with the Arlequin program. HLA-A, -B, -C, -DRB1, -DQB1 and -DPB1 alleles were compared between patients with COVID-19 and 99 healthy controls. We identified that COVID-19 susceptibility is associated with alleles and genotypes rs9277534A (disequilibrium with HLA-DPB1*02:01, -02:02, -04:01, -04:02, -17:01 alleles) with low expression of protein products HLA-DPB1 (pc < 0.028) and homozygosity at HLA-C*04 (p = 0.024, pc = 0.312). Allele HLA-A*01:01 was decreased in a group of patients with severe forms of bilateral pneumonia, and therefore it may be considered as a protective factor for the development of severe symptoms of COVID-19 (p = 0.009, pc = 0.225). Our studies provide further evidence for the functional association between HLA genes and COVID-19. (c) 2022 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:547 / 550
页数:4
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