The role of HLA genotypes in understanding the pathogenesis of severe COVID-19.

Fatemeh Arab, Samaneh Mollazadeh, Farnaz Ghayourbabaei, Meysam Moghbeli, Ehsan Saburi
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Abstract

The coronavirus disease 2019 (COVID-19) pandemic has caused human tragedy through the global spread of the viral pathogen SARS-CoV-2. Although the underlying factors for the severity of COVID-19 in different people are still unknown, several gene variants can be used as predictors of disease severity, particularly variations in viral receptor genes such as angiotensin-converting enzyme 2 (ACE2) or major histocompatibility complex (MHC) genes. The reaction of the immune system, as the most important defense strategy in the case of viruses, plays a decisive role. The innate immune system is important both as a primary line of defense and as a trigger of the acquired immune response. The HLA-mediated acquired immune response is linked to the acquired immune system. In various diseases, it has been shown that genetic alterations in components of the immune system can play a crucial role in how the body responds to pathogens, especially viruses. One of the most important host genetic factors is the human leukocyte antigen (HLA) profile, which includes HLA classes I and II and may be symbolic of the diversity of immune response and genetic predisposition in disease progression. COVID-19 will have direct contact with the acquired immune system as an intracellular pathogen after exposure to the proteasome and its components through class I HLA. Therefore, it is assumed that in different genotypes of the HLA-I class, an undesirable supply causes an insufficient activation of the immune system. Insufficient binding of antigen delivered by class I HLA to host lymphocytes results in uncertain identification and insufficient activation of the acquired immune system. The absence of secretion of immune cytokines such as interferons, which play an important role in controlling viral infection in the early stages, is a complication of this event. Understanding the allelic diversity of HLA in people infected with coronavirus compared with uninfected people of one race not only allows identification of people with HLA susceptible to COVID-19 but also provides better insight into the behavior of the virus, which helps to take effective preventive and curative measures earlier.

Abstract Image

HLA 基因型在了解严重 COVID-19 发病机制中的作用。
2019 年冠状病毒病(COVID-19)大流行通过病毒病原体 SARS-CoV-2 的全球传播造成了人类悲剧。尽管不同人群感染 COVID-19 的严重程度的潜在因素尚不清楚,但有几种基因变异可作为疾病严重程度的预测因子,特别是血管紧张素转换酶 2(ACE2)或主要组织相容性复合体(MHC)基因等病毒受体基因的变异。免疫系统的反应是病毒最重要的防御策略,起着决定性的作用。先天性免疫系统既是第一道防线,也是后天免疫反应的触发器。HLA 介导的获得性免疫反应与后天免疫系统有关。在各种疾病中,免疫系统各组成部分的基因改变在机体如何应对病原体(尤其是病毒)方面起着至关重要的作用。人类白细胞抗原(HLA)图谱是最重要的宿主遗传因素之一,它包括 HLA I 类和 II 类,可能象征着免疫反应的多样性和疾病进展中的遗传易感性。COVID-19 通过 I 类 HLA 暴露于蛋白酶体及其成分后,将作为细胞内病原体与获得性免疫系统直接接触。因此,假定在不同的 HLA-I 类基因型中,不良供应会导致免疫系统激活不足。I 类 HLA 递送的抗原与宿主淋巴细胞结合不充分,导致识别不确定和获得性免疫系统激活不充分。免疫细胞因子(如干扰素)在早期控制病毒感染中发挥着重要作用,而这种细胞因子分泌的缺失则是这一事件的并发症。了解冠状病毒感染者与同一种族未感染者相比的 HLA 等位基因多样性,不仅可以识别 HLA 易感 COVID-19 的人群,还能更好地了解病毒的行为,有助于尽早采取有效的预防和治疗措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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