P. A. Talyzin, A. Myasnikov, S. Berns, M. Ilyina, A. Komazov, V. Lynyov, E. V. Ekusheva
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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":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"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. 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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\":\"1 1\",\"pages\":\"\"},\"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}","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
摘要
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。
Preventive effectiveness of nasal interferon-gamma among adult volunteers against acute respiratory viral infections, including COVID-19
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.