IL17A、IL17F和ILR1N多态性与COVID-19严重程度的关系研究:IL17A rs2275913多态性在COVID-19临床病程中的预测作用

IF 2.3 4区 医学 Q3 GENETICS & HEREDITY International Journal of Immunogenetics Pub Date : 2023-04-13 DOI:10.1111/iji.12619
Gunes Cakmak Genc, Sevim Karakas Celik, Busra Yilmaz, Nihal Piskin, Bulent Altinsoy, Ahmet Dursun
{"title":"IL17A、IL17F和ILR1N多态性与COVID-19严重程度的关系研究:IL17A rs2275913多态性在COVID-19临床病程中的预测作用","authors":"Gunes Cakmak Genc,&nbsp;Sevim Karakas Celik,&nbsp;Busra Yilmaz,&nbsp;Nihal Piskin,&nbsp;Bulent Altinsoy,&nbsp;Ahmet Dursun","doi":"10.1111/iji.12619","DOIUrl":null,"url":null,"abstract":"<p>Coronavirus disease 2019 (COVID-19) is an infectious respiratory disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Although the mortality rate of the disease has been relatively under control as of 2022, more than 15 million confirmed COVID-19 cases have been detected in Turkey to date, causing more than 100,000 deaths. The clinical manifestation of the disease varies widely, ranging from asymptomatic to acute respiratory distress syndrome causing death. The immune response mechanisms have an important impact on the fine adjustment between healing and enhanced tissue damage. This study aims to investigate the relationship between the variants of the <i>interleukin 1 receptor antagonist (IL1RN), interleukin 17A (IL17A)</i>, and <i>interleukin 17F (IL17F)</i> genes and COVID-19 severity. The study population comprised 202 confirmed COVID-19 cases divided into three groups according to severity. The <i>IL1RN</i> variable number of a tandem repeat (VNTR) polymorphism was genotyped by polymerase chain reaction (PCR), and <i>IL17A</i> rs2275913, <i>IL17F</i> rs763780 and rs2397084 polymorphisms were genotyped by the PCR-based restriction fragment length polymorphism method. Statistical analysis revealed a significant association between <i>IL17A</i> rs2275913 variant and COVID-19 severity. The AA genotype and the A allele of <i>IL17A</i> rs2275913 were found significant in the severe group. Additionally, we found a significant relationship between haplotype frequency distributions and severity of COVID-19 for the <i>IL17F</i> rs763780/rs2397084 (p = 0.044) and a combination of <i>IL17F</i> rs763780/rs2397084/ <i>IL17A</i> rs2275913 (p = 0.04). The CG and CGA haplotype frequencies were significantly higher in the severe group. <i>IL17A</i> rs2275913, <i>IL17F</i> rs763780 and rs2397084 variants appear to have important effects on the immune response in COVID-19. In conclusion, variants of <i>IL17A</i> rs2275913, <i>IL17F</i> rs763780 and rs2397084 may be the predictive markers for the clinical course and potential immunomodulatory treatment options in COVID-19, a disease that has placed a significant burden on our country.</p>","PeriodicalId":14003,"journal":{"name":"International Journal of Immunogenetics","volume":"50 3","pages":"117-126"},"PeriodicalIF":2.3000,"publicationDate":"2023-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Investigation of the relationship between IL17A, IL17F and ILR1N polymorphisms and COVID-19 severity: The predictive role of IL17A rs2275913 polymorphism in the clinical course of COVID-19\",\"authors\":\"Gunes Cakmak Genc,&nbsp;Sevim Karakas Celik,&nbsp;Busra Yilmaz,&nbsp;Nihal Piskin,&nbsp;Bulent Altinsoy,&nbsp;Ahmet Dursun\",\"doi\":\"10.1111/iji.12619\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Coronavirus disease 2019 (COVID-19) is an infectious respiratory disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Although the mortality rate of the disease has been relatively under control as of 2022, more than 15 million confirmed COVID-19 cases have been detected in Turkey to date, causing more than 100,000 deaths. The clinical manifestation of the disease varies widely, ranging from asymptomatic to acute respiratory distress syndrome causing death. The immune response mechanisms have an important impact on the fine adjustment between healing and enhanced tissue damage. This study aims to investigate the relationship between the variants of the <i>interleukin 1 receptor antagonist (IL1RN), interleukin 17A (IL17A)</i>, and <i>interleukin 17F (IL17F)</i> genes and COVID-19 severity. The study population comprised 202 confirmed COVID-19 cases divided into three groups according to severity. The <i>IL1RN</i> variable number of a tandem repeat (VNTR) polymorphism was genotyped by polymerase chain reaction (PCR), and <i>IL17A</i> rs2275913, <i>IL17F</i> rs763780 and rs2397084 polymorphisms were genotyped by the PCR-based restriction fragment length polymorphism method. Statistical analysis revealed a significant association between <i>IL17A</i> rs2275913 variant and COVID-19 severity. The AA genotype and the A allele of <i>IL17A</i> rs2275913 were found significant in the severe group. Additionally, we found a significant relationship between haplotype frequency distributions and severity of COVID-19 for the <i>IL17F</i> rs763780/rs2397084 (p = 0.044) and a combination of <i>IL17F</i> rs763780/rs2397084/ <i>IL17A</i> rs2275913 (p = 0.04). The CG and CGA haplotype frequencies were significantly higher in the severe group. <i>IL17A</i> rs2275913, <i>IL17F</i> rs763780 and rs2397084 variants appear to have important effects on the immune response in COVID-19. In conclusion, variants of <i>IL17A</i> rs2275913, <i>IL17F</i> rs763780 and rs2397084 may be the predictive markers for the clinical course and potential immunomodulatory treatment options in COVID-19, a disease that has placed a significant burden on our country.</p>\",\"PeriodicalId\":14003,\"journal\":{\"name\":\"International Journal of Immunogenetics\",\"volume\":\"50 3\",\"pages\":\"117-126\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2023-04-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Immunogenetics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/iji.12619\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Immunogenetics","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/iji.12619","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

摘要

冠状病毒病2019 (COVID-19)是由严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)引起的一种传染性呼吸道疾病。尽管截至2022年,该疾病的死亡率已相对得到控制,但迄今为止,土耳其已发现1500多万例COVID-19确诊病例,造成10万多人死亡。该病的临床表现差异很大,从无症状到可导致死亡的急性呼吸窘迫综合征。免疫应答机制对愈合与组织损伤增强之间的精细调节有重要影响。本研究旨在探讨白细胞介素1受体拮抗剂(IL1RN)、白细胞介素17A (IL17A)和白细胞介素17F (IL17F)基因变异与COVID-19严重程度的关系。研究人群包括202例新冠肺炎确诊病例,根据严重程度分为三组。采用聚合酶链反应(PCR)对IL1RN可变数目串联重复序列(VNTR)多态性进行基因分型,采用基于PCR的限制性片段长度多态性方法对IL17A rs2275913、IL17F rs763780和rs2397084多态性进行基因分型。统计分析显示IL17A rs2275913变异与COVID-19严重程度显著相关。重度组AA基因型和IL17A rs2275913等位基因A显著。此外,我们发现IL17F rs763780/rs2397084单倍型频率分布与COVID-19严重程度之间存在显著关系(p = 0.044), IL17F rs763780/rs2397084/ IL17A rs2275913的组合(p = 0.04)。重度组的CG和CGA单倍型频率显著增高。IL17A rs2275913、IL17F rs763780和rs2397084变体似乎对COVID-19的免疫反应有重要影响。总之,IL17A rs2275913、IL17F rs763780和rs2397084变异可能是COVID-19临床病程和潜在免疫调节治疗方案的预测指标,这一疾病给我国带来了重大负担。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Investigation of the relationship between IL17A, IL17F and ILR1N polymorphisms and COVID-19 severity: The predictive role of IL17A rs2275913 polymorphism in the clinical course of COVID-19

Coronavirus disease 2019 (COVID-19) is an infectious respiratory disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Although the mortality rate of the disease has been relatively under control as of 2022, more than 15 million confirmed COVID-19 cases have been detected in Turkey to date, causing more than 100,000 deaths. The clinical manifestation of the disease varies widely, ranging from asymptomatic to acute respiratory distress syndrome causing death. The immune response mechanisms have an important impact on the fine adjustment between healing and enhanced tissue damage. This study aims to investigate the relationship between the variants of the interleukin 1 receptor antagonist (IL1RN), interleukin 17A (IL17A), and interleukin 17F (IL17F) genes and COVID-19 severity. The study population comprised 202 confirmed COVID-19 cases divided into three groups according to severity. The IL1RN variable number of a tandem repeat (VNTR) polymorphism was genotyped by polymerase chain reaction (PCR), and IL17A rs2275913, IL17F rs763780 and rs2397084 polymorphisms were genotyped by the PCR-based restriction fragment length polymorphism method. Statistical analysis revealed a significant association between IL17A rs2275913 variant and COVID-19 severity. The AA genotype and the A allele of IL17A rs2275913 were found significant in the severe group. Additionally, we found a significant relationship between haplotype frequency distributions and severity of COVID-19 for the IL17F rs763780/rs2397084 (p = 0.044) and a combination of IL17F rs763780/rs2397084/ IL17A rs2275913 (p = 0.04). The CG and CGA haplotype frequencies were significantly higher in the severe group. IL17A rs2275913, IL17F rs763780 and rs2397084 variants appear to have important effects on the immune response in COVID-19. In conclusion, variants of IL17A rs2275913, IL17F rs763780 and rs2397084 may be the predictive markers for the clinical course and potential immunomodulatory treatment options in COVID-19, a disease that has placed a significant burden on our country.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
4.70
自引率
0.00%
发文量
48
审稿时长
6-12 weeks
期刊介绍: The International Journal of Immunogenetics (formerly European Journal of Immunogenetics) publishes original contributions on the genetic control of components of the immune system and their interactions in both humans and experimental animals. The term ''genetic'' is taken in its broadest sense to include studies at the evolutionary, molecular, chromosomal functional and population levels in both health and disease. Examples are: -studies of blood groups and other surface antigens- cell interactions and immune response- receptors, antibodies, complement components and cytokines- polymorphism- evolution of the organisation, control and function of immune system components- anthropology and disease associations- the genetics of immune-related disease: allergy, autoimmunity, immunodeficiency and other immune pathologies- All papers are seen by at least two independent referees and only papers of the highest quality are accepted.
期刊最新文献
Association of PADI4 Gene Polymorphisms With Susceptibility to Rheumatoid Arthritis: Evidence From 24 Case-Control Studies. Associations Between Interleukin-10 Polymorphisms and Susceptibility to Sjögren's Syndrome: A Meta-Analysis. Issue Information Nomenclature for factors of the HLA system, update July, August and September 2024 Role of C–C chemokine receptor type 5 in pathogenesis of malaria and its severe forms
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1