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新型冠状病毒肺炎患者主要组织相容性复合体Ⅰ类链相关基因 A(MICA)短串联重复序列多态性。

Major Histocompatibility Complex Class I Chain-Related α (MICA) STR Polymorphisms in COVID-19 Patients.

机构信息

Servicio de Análisis Clínicos e Inmunología, Hospital Universitario Virgen de las Nieves, 18012 Granada, Spain.

Programa de Doctorado en Biomedicina, University of Granada, 18016 Granada, Spain.

出版信息

Int J Mol Sci. 2022 Jun 23;23(13):6979. doi: 10.3390/ijms23136979.

Abstract

The SARS-CoV-2 disease presents different phenotypes of severity. Comorbidities, age, and being overweight are well established risk factors for severe disease. However, innate immunity plays a key role in the early control of viral infections and may condition the gravity of COVID-19. Natural Killer (NK) cells are part of innate immunity and are important in the control of virus infection by killing infected cells and participating in the development of adaptive immunity. Therefore, we studied the short tandem repeat (STR) transmembrane polymorphisms of the major histocompatibility complex class I chain-related A (MICA), an NKG2D ligand that induces activation of NK cells, among other cells. We compared the alleles and genotypes of MICA in COVID-19 patients versus healthy controls and analyzed their relation to disease severity. Our results indicate that the MICAA9 allele is related to infection as well as to symptomatic disease but not to severe disease. The MICAA9 allele may be a risk factor for SARS-CoV-2 infection and symptomatic disease.

摘要

SARS-CoV-2 疾病表现出不同严重程度的表型。合并症、年龄和超重是严重疾病的既定危险因素。然而,先天免疫在控制病毒感染方面起着关键作用,并且可能影响 COVID-19 的严重程度。自然杀伤 (NK) 细胞是先天免疫的一部分,通过杀死感染细胞和参与适应性免疫的发展来控制病毒感染非常重要。因此,我们研究了主要组织相容性复合体 I 类链相关 A(MICA)的短串联重复(STR)跨膜多态性,MICA 是一种 NKG2D 配体,可诱导 NK 细胞激活以及其他细胞的激活。我们比较了 COVID-19 患者与健康对照组的 MICA 等位基因和基因型,并分析了它们与疾病严重程度的关系。我们的结果表明,MICAA9 等位基因与感染以及症状性疾病有关,但与严重疾病无关。MICAA9 等位基因可能是 SARS-CoV-2 感染和症状性疾病的危险因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6e3/9266713/3b04b6fd1184/ijms-23-06979-g001.jpg

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