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HLA基因型在理解重症COVID-19发病机制中的作用。

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

作者信息

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

机构信息

Medical Genetics and Molecular Medicine Department, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

Natural Products and Medicinal Plants Research Center, North Khorasan University of Medical Sciences, Bojnurd, Iran.

出版信息

Egypt J Med Hum Genet. 2023;24(1):14. doi: 10.1186/s43042-023-00392-3. Epub 2023 Jan 26.

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.

摘要

2019年冠状病毒病(COVID-19)大流行通过病毒病原体严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的全球传播造成了人类悲剧。尽管不同人群中COVID-19严重程度的潜在因素仍不清楚,但几种基因变异可作为疾病严重程度的预测指标,特别是病毒受体基因的变异,如血管紧张素转换酶2(ACE2)或主要组织相容性复合体(MHC)基因。免疫系统的反应作为病毒感染时最重要的防御策略,起着决定性作用。先天免疫系统作为主要防线以及获得性免疫反应的触发因素都很重要。HLA介导的获得性免疫反应与获得性免疫系统相关。在各种疾病中,已经表明免疫系统组成部分的基因改变在机体对病原体尤其是病毒的反应方式中可发挥关键作用。最重要的宿主遗传因素之一是人类白细胞抗原(HLA)谱,它包括I类和II类HLA,可能象征着免疫反应的多样性以及疾病进展中的遗传易感性。COVID-19作为一种细胞内病原体,在通过I类HLA暴露于蛋白酶体及其成分后,将与获得性免疫系统直接接触。因此,推测在I类HLA的不同基因型中,不良的供应会导致免疫系统激活不足。I类HLA递呈的抗原与宿主淋巴细胞的结合不足会导致获得性免疫系统的识别不确定和激活不足。在早期控制病毒感染中起重要作用的免疫细胞因子如干扰素分泌缺乏是这一事件的并发症。了解感染冠状病毒的人与未感染同一种族的人相比HLA的等位基因多样性,不仅可以识别对COVID-19易感的HLA人群,还能更好地洞察病毒的行为,这有助于更早地采取有效的预防和治疗措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adb9/9878497/2402101a0960/43042_2023_392_Fig1_HTML.jpg

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