{"title":"Human Leukocyte Antigen as a Predictor of COVID-19 Severity","authors":"A. Jandaghi, Afshin Samiei, Narges Khaghanzadeh","doi":"10.34172/hmj.2022.27","DOIUrl":null,"url":null,"abstract":"Since the spread of the coronavirus disease 2019 (COVID-19) pandemic, many countries have been suffering from the disease, and patients exhibit an extensive spectrum of symptoms from mild to severe, and in some cases, it leads to death. Identifying vulnerability factors may help detect very high-risk subjects to prevent disease mortality. Since people have different human leukocyte antigen (HLA) alleles, and the frequency of the alleles varies between different races and geographic regions, it is inferred that there is an association between HLA and the vulnerability of the population. The present study aimed to find the most frequent HLA alleles that profoundly affect COVID-19 outcomes. To find the relevant articles, medical databases (Medline, PubMed, EMBASE, Cochrane Library, and the like) were searched by the keywords, and the results related to the association between HLA and COVID-19 morbidity were selected and briefly presented. Regarding the extracted information from several studies, HLA alleles with a strong affinity to COVID-19 epitopes such as HLA-A*11:01, HLA-A*02:06, and HLA-B*54:01 could result in mild symptoms, while those with weak affinity such as HLA-B*44:06 and HLA-B*46:01 contributed to severe symptoms and high mortality rate. Further, heterozygosity and frequency of HLA alleles could affect the disease outcome within populations. As a result, the vulnerability of the patients can be predicted through their HLA pattern, and preventive measures can be taken instantly for populations expressing high-risk alleles. HLA can be assumed as a global predictor of COVID-19 disease outcomes. High frequent alleles which affect the outcome of the disease are introduced as susceptibility-determining alleles.","PeriodicalId":271947,"journal":{"name":"Hormozgan Medical Journal","volume":"24 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hormozgan Medical Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.34172/hmj.2022.27","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Since the spread of the coronavirus disease 2019 (COVID-19) pandemic, many countries have been suffering from the disease, and patients exhibit an extensive spectrum of symptoms from mild to severe, and in some cases, it leads to death. Identifying vulnerability factors may help detect very high-risk subjects to prevent disease mortality. Since people have different human leukocyte antigen (HLA) alleles, and the frequency of the alleles varies between different races and geographic regions, it is inferred that there is an association between HLA and the vulnerability of the population. The present study aimed to find the most frequent HLA alleles that profoundly affect COVID-19 outcomes. To find the relevant articles, medical databases (Medline, PubMed, EMBASE, Cochrane Library, and the like) were searched by the keywords, and the results related to the association between HLA and COVID-19 morbidity were selected and briefly presented. Regarding the extracted information from several studies, HLA alleles with a strong affinity to COVID-19 epitopes such as HLA-A*11:01, HLA-A*02:06, and HLA-B*54:01 could result in mild symptoms, while those with weak affinity such as HLA-B*44:06 and HLA-B*46:01 contributed to severe symptoms and high mortality rate. Further, heterozygosity and frequency of HLA alleles could affect the disease outcome within populations. As a result, the vulnerability of the patients can be predicted through their HLA pattern, and preventive measures can be taken instantly for populations expressing high-risk alleles. HLA can be assumed as a global predictor of COVID-19 disease outcomes. High frequent alleles which affect the outcome of the disease are introduced as susceptibility-determining alleles.
自2019年冠状病毒病(COVID-19)大流行传播以来,许多国家都遭受了这种疾病的困扰,患者表现出从轻微到严重的广泛症状,在某些情况下还会导致死亡。确定易感因素可能有助于发现高危人群,以预防疾病死亡。由于人类白细胞抗原(HLA)等位基因不同,且等位基因的频率在不同种族和地理区域之间存在差异,因此可以推断HLA与人群易感性之间存在关联。本研究旨在找到影响COVID-19预后的最常见HLA等位基因。通过关键词检索医学数据库(Medline、PubMed、EMBASE、Cochrane Library等)查找相关文献,选取HLA与COVID-19发病相关的结果并简要介绍。从多项研究提取的信息来看,HLA- a *11:01、HLA- a *02:06、HLA- b *54:01等与COVID-19表位亲和力较强的HLA等位基因可导致症状较轻,HLA- b *44:06、HLA- b *46:01等亲和力较弱的HLA等位基因可导致症状较重、死亡率较高。此外,HLA等位基因的杂合性和频率可能影响人群内的疾病结果。因此,可以通过HLA型预测患者的易感性,对表达高危等位基因的人群及时采取预防措施。HLA可以被认为是COVID-19疾病结局的全球预测因子。影响疾病结果的高频率等位基因被引入作为决定易感性的等位基因。