Preventive effectiveness of nasal interferon-gamma among adult volunteers against acute respiratory viral infections, including COVID-19

Q4 Immunology and Microbiology Immunologiya Pub Date : 2022-01-01 DOI:10.33029/0206-4952-2022-43-3-301-311
P. A. Talyzin, A. Myasnikov, S. Berns, M. Ilyina, A. Komazov, V. Lynyov, E. V. Ekusheva
{"title":"Preventive effectiveness of nasal interferon-gamma among adult volunteers against acute respiratory viral infections, including COVID-19","authors":"P. A. Talyzin, A. Myasnikov, S. Berns, M. Ilyina, A. Komazov, V. Lynyov, E. V. Ekusheva","doi":"10.33029/0206-4952-2022-43-3-301-311","DOIUrl":null,"url":null,"abstract":"Background. In vitro studies showed effective viral infection block in case of pretreatment with exogenous interferons. Interferon-gamma is a unique immune interferon, actively expressed in patients with acute respiratory viral infections (ARVI) and defending the body from severe infection course. Aim - to evaluate the safety and preventive effectiveness of nasal interferon-gamma protecting against ARVI, including COVID-19. Material and methods. The study enrolled 630 adult volunteers with a negative PCR test result for SARS-CoV-2, without respiratory symptoms and contraindications to interferongamma. Participants were randomized (1 : 1) into 2 groups: the study group - with the use of a prophylactic course of nasal interferon-gamma, and the group of comparison - without a course of prophylaxis. All participants were given a diary for daily monitor respiratory symptoms, adverse events, and record the use of pharmacotherapy. Results. Safety analysis found no differences between groups. During 28 days period a higher incidence of ARVI, including COVID-19, was observed in the group of comparison (13 vs 3 cases in the study group). The odd ratio was 0.224 (95 % CI: 0.040-0.826), p = 0.020. The total number of ARVI cases, including COVID-19, in the group of comparison during 2 months of research was 26 vs 6 in the study group. The odd ratio was 0.233 (95 % CI: 0.077- 0.594), p = 0,001. The longest period of persistence of respiratory symptoms was obtained in the group of comparison (7 vs 4 days in the study group, p = 0.034). Conclusion. Nasal interferon-gamma as a preventive measure contributes to a decrease of infection incidence of ARVI, including COVID-19.","PeriodicalId":38750,"journal":{"name":"Immunologiya","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Immunologiya","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.33029/0206-4952-2022-43-3-301-311","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Immunology and Microbiology","Score":null,"Total":0}
引用次数: 1

Abstract

Background. In vitro studies showed effective viral infection block in case of pretreatment with exogenous interferons. Interferon-gamma is a unique immune interferon, actively expressed in patients with acute respiratory viral infections (ARVI) and defending the body from severe infection course. Aim - to evaluate the safety and preventive effectiveness of nasal interferon-gamma protecting against ARVI, including COVID-19. Material and methods. The study enrolled 630 adult volunteers with a negative PCR test result for SARS-CoV-2, without respiratory symptoms and contraindications to interferongamma. Participants were randomized (1 : 1) into 2 groups: the study group - with the use of a prophylactic course of nasal interferon-gamma, and the group of comparison - without a course of prophylaxis. All participants were given a diary for daily monitor respiratory symptoms, adverse events, and record the use of pharmacotherapy. Results. Safety analysis found no differences between groups. During 28 days period a higher incidence of ARVI, including COVID-19, was observed in the group of comparison (13 vs 3 cases in the study group). The odd ratio was 0.224 (95 % CI: 0.040-0.826), p = 0.020. The total number of ARVI cases, including COVID-19, in the group of comparison during 2 months of research was 26 vs 6 in the study group. The odd ratio was 0.233 (95 % CI: 0.077- 0.594), p = 0,001. The longest period of persistence of respiratory symptoms was obtained in the group of comparison (7 vs 4 days in the study group, p = 0.034). Conclusion. Nasal interferon-gamma as a preventive measure contributes to a decrease of infection incidence of ARVI, including COVID-19.
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
成人志愿者鼻用γ干扰素对急性呼吸道病毒感染(包括COVID-19)的预防效果
背景。体外研究表明,在外源性干扰素预处理的情况下,有效的病毒感染阻断。干扰素- γ是一种独特的免疫干扰素,在急性呼吸道病毒感染(ARVI)患者中积极表达,保护身体免受严重感染。目的:评价鼻用γ干扰素预防ARVI(包括COVID-19)的安全性和有效性。材料和方法。该研究招募了630名成年志愿者,他们的PCR检测结果为SARS-CoV-2阴性,没有呼吸道症状和干扰素的禁忌症。参与者被随机(1:1)分为两组:研究组-使用预防性鼻干扰素- γ疗程,对照组-不使用预防性疗程。所有参与者都被给予日记,用于每日监测呼吸系统症状、不良事件,并记录药物治疗的使用情况。结果。安全性分析没有发现组间差异。在28天期间,对照组观察到包括COVID-19在内的ARVI发病率较高(13例vs研究组3例)。奇比为0.224 (95% CI: 0.040-0.826), p = 0.020。在2个月的研究期间,对照组包括COVID-19在内的ARVI病例总数为26例,而研究组为6例。奇比为0.233 (95% CI: 0.077 ~ 0.594), p = 0.001。对照组呼吸系统症状持续时间最长(7天vs研究组4天,p = 0.034)。结论。鼻用干扰素作为预防措施有助于降低ARVI感染的发生率,包括COVID-19。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Immunologiya
Immunologiya Immunology and Microbiology-Immunology
CiteScore
1.90
自引率
0.00%
发文量
31
期刊最新文献
Severe course of HAE and a new variant of the SERPING1 gene in a large Caucasian family MIR 19® – world first specific antiviral drug for COVID-19 treatment: development and preclinical studies Cellular and humoral responses to SARS-CoV-2 (omicron variant) in children and adolescents with pulmonary tuberculosis Methodology for evaluation of the level of IgG antibodies against different SARS-CoV-2 proteins using multiplex immunofluorescence analysis Comparison of transcriptional profiles of human macrophages activated by agonists of NOD1 and TLR4 receptors
×
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