首页 > 最新文献

Immunologiya最新文献

英文 中文
Phenotypic and functional features of in vitro generated TCR-T cells specific for the tumor-associated antigen NY-ESO-1 体外生成的肿瘤相关抗原NY-ESO-1特异性TCR-T细胞的表型和功能特征
Q4 Immunology and Microbiology Pub Date : 2022-01-01 DOI: 10.33029/0206-4952-2022-43-5-536-547
M. Kuznetsova, V. Tereshchenko, Y. Shevchenko, M. Fisher, V. Kurilin, A. Alsalloum, S. Alrhmoun, Y. Akahori, H. Shiku, S. Sennikov
{"title":"Phenotypic and functional features of in vitro generated TCR-T cells specific for the tumor-associated antigen NY-ESO-1","authors":"M. Kuznetsova, V. Tereshchenko, Y. Shevchenko, M. Fisher, V. Kurilin, A. Alsalloum, S. Alrhmoun, Y. Akahori, H. Shiku, S. Sennikov","doi":"10.33029/0206-4952-2022-43-5-536-547","DOIUrl":"https://doi.org/10.33029/0206-4952-2022-43-5-536-547","url":null,"abstract":"","PeriodicalId":38750,"journal":{"name":"Immunologiya","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69482292","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Preventive effectiveness of nasal interferon-gamma among adult volunteers against acute respiratory viral infections, including COVID-19 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
Q4 Immunology and Microbiology 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
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.
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。
{"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":"https://doi.org/10.33029/0206-4952-2022-43-3-301-311","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":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69481770","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
New approaches to allergen-specific immunotherapy (ASIT): development of a recombinant vaccine against birch pollen allergy 过敏原特异性免疫治疗(ASIT)的新途径:桦树花粉过敏重组疫苗的研制
Q4 Immunology and Microbiology Pub Date : 2022-01-01 DOI: 10.33029/0206-4952-2022-42-6-621-631
O. Elisyutina, N. Shershakova, V. Smirnov, I. Shilovskiy, A. Korneev, A. Poroshina, E. V. Smolnikov, A. Litovkina, E.S. Fedenko , D. Kudlay, R. Valenta, M. Khaitov
{"title":"New approaches to allergen-specific immunotherapy (ASIT): development of a recombinant vaccine against birch pollen allergy","authors":"O. Elisyutina, N. Shershakova, V. Smirnov, I. Shilovskiy, A. Korneev, A. Poroshina, E. V. Smolnikov, A. Litovkina, E.S. Fedenko , D. Kudlay, R. Valenta, M. Khaitov","doi":"10.33029/0206-4952-2022-42-6-621-631","DOIUrl":"https://doi.org/10.33029/0206-4952-2022-42-6-621-631","url":null,"abstract":"","PeriodicalId":38750,"journal":{"name":"Immunologiya","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69481778","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Post-vaccination and post-infection humoral immune response to the SARS-CoV-2 infection 疫苗接种后和感染后对SARS-CoV-2感染的体液免疫反应
Q4 Immunology and Microbiology Pub Date : 2022-01-01 DOI: 10.33029/0206-4952-2022-43-1-18-32
I. V. Andreev, K.O. Nechay, A. I. Andreev, A.P. Zubaryova, D. R. Esaulova, A.M. Alenova, I.А. Nikolaeva , O. P. Chernyavskaya, K. S. Lomonosov, A. Shulzhenko, O. Kurbacheva, E. Latysheva, N. Shartanova, E. Nazarova, L. Romanova, N. Cherchenko, V. Smirnov, O. Averkov, А. Martynov, V. Vechorko, G. Gudima, D. Kudlay, R. Khaitov, M. Khaitov
Introduction. Mass vaccination of the population against SARS-CoV-2 in Russia and abroad has been going on for more than 2 years. Various types of vaccines are used for vaccination (vector vaccines, RNA vaccines, whole-virion vaccines). The first in the world was registered the Russian vector vaccine «Gam-COVID-Vac» («Sputnik V»), which is widely used in our country, as well as in many other countries of the world. An important area of research is the monitoring of the parameters of the vaccine-induced immune response their analysis in relation to the characteristics of the immune response caused by SARSCoV-2 infection/COVID-19. Such studies are important both for assessing the intensity and duration of post-vaccination immunity, and for improving strategies for immunoprophylaxis and immunotherapy of coronavirus infection. The article presents the results of a study of the humoral immune response in patients with COVID-19 and vaccinated with «Sputnik V» in the period from autumn 2020 till the present time. The aim of the work - a comparative study of the humoral immune response to SARSCoV-2 infection and vaccination against COVID-19. Material and methods. The content of antibodies against SARS-CoV-2 S- and N-proteins was studied in 449 blood serum samples of men and women (age 25-65 years). 5 groups of samples were formed: suffered from COVID-19 of mild and moderate severity, at different times after recovery (262 samples);immunized with the «Sputnik V» vaccine, at different times after injection of the 2nd component of «Sputnik V» (104 samples);suffered from COVID-19 of mild and moderate severity, and then vaccinated with «Sputnik V» (53 samples);vaccinated with «Sputnik V», and then suffered with COVID-19 (12 samples);revaccinated with the vaccine «Sputnik Light» (18 samples). Results. To assess the content of IgG antibodies to S-protein and to N-protein of SARSCoV-2 in human blood sera, an EIA diagnostic system was developed further certified by the Ministry of Health of Russian Federation. In people suffered COVID-19 in 90 % of cases the positive levels of IgG antibodies to SARS-CoV-2 S-protein persist 9 months after recovery, while the proportion of potential plasma donors and material for obtaining intravenous immunoglobulin with a high content of IgG antibodies to S-protein 1 month after the disease is 20 %. In 76 % of people vaccinated with «Sputnik V» high levels of IgG antibodies to S-protein are detected within 6 months after the course of vaccination. The content of IgG antibodies to S-protein in the blood sera of persons suffered COVID-19, and then 6 months after recovery vaccinated with the 1st component of the vaccine «Sputnik V» in 100 % of cases was high with a positivity coefficient above 8.1, regardless of the initial value, already on 7 and 21 days after injection. In persons vaccinated with «Sputnik V» and then passed COVID-19, a high content of S-specific IgG antibodies is observed in 100 % of cases. The examination of vacci
介绍。在俄罗斯和国外,针对SARS-CoV-2的大规模人群疫苗接种已经进行了2年多。疫苗接种使用各种类型的疫苗(载体疫苗、RNA疫苗、全病毒粒子疫苗)。世界上第一个注册的是俄罗斯病媒疫苗“Gam-COVID-Vac”(“Sputnik V”),该疫苗在我国以及世界上许多其他国家广泛使用。一个重要的研究领域是监测疫苗诱导的免疫反应参数,并分析其与SARSCoV-2感染/COVID-19引起的免疫反应特征的关系。这些研究对于评估疫苗接种后免疫的强度和持续时间,以及改进冠状病毒感染的免疫预防和免疫治疗策略都具有重要意义。本文介绍了2020年秋季至今接种“人造卫星V”疫苗的COVID-19患者体液免疫反应的研究结果。这项工作的目的是对SARSCoV-2感染和COVID-19疫苗接种的体液免疫反应进行比较研究。材料和方法。研究了449例25-65岁男性和女性血清样本中SARS-CoV-2 S-和n -蛋白抗体的含量。5组样本形成:遭受COVID-19轻度和中度严重程度,在不同的时间后恢复(262个样本);与«Sputnik V»疫苗接种,在不同的时间后注射第二组成部分«Sputnik V»(104个样本);遭受COVID-19轻度和中度严重程度,然后接种«Sputnik V»(53个样品);接种«Sputnik V»,然后遭受COVID-19样本(12);保存下来的疫苗«人造卫星光»(18样本)。结果。为评估人血清SARSCoV-2 s蛋白和n蛋白IgG抗体的含量,开发了经俄罗斯联邦卫生部进一步认证的EIA诊断系统。在90%的COVID-19患者中,SARS-CoV-2 s蛋白IgG抗体在康复后9个月仍呈阳性水平,而潜在血浆供体和在发病后1个月获得高含量s蛋白IgG抗体的静脉注射免疫球蛋白的比例为20%。在接种“Sputnik V”疫苗的人中,76%的人在接种过程后6个月内检测到高水平的s蛋白IgG抗体。在感染COVID-19的人,然后在康复6个月后接种疫苗“Sputnik V”第一组分的病例中,100%的病例在注射后7天和21天的血清中s蛋白IgG抗体含量很高,阳性系数大于8.1,无论初始值如何。在接种“Sputnik V”疫苗然后通过COVID-19的人中,100%的病例中观察到高含量的s特异性IgG抗体。对接种过“Sputnik Light”疫苗的人进行的检查显示,对s蛋白的抗体水平100%高。结论。该检测系统可用于评估COVID-19患者、疫苗接种者和再接种者的SARS-CoV-2抗原IgG抗体含量。所进行的研究表明,接种疫苗后有6个月的强化免疫,感染后有9个月的强化免疫。
{"title":"Post-vaccination and post-infection humoral immune response to the SARS-CoV-2 infection","authors":"I. V. Andreev, K.O. Nechay, A. I. Andreev, A.P. Zubaryova, D. R. Esaulova, A.M. Alenova, I.А. Nikolaeva , O. P. Chernyavskaya, K. S. Lomonosov, A. Shulzhenko, O. Kurbacheva, E. Latysheva, N. Shartanova, E. Nazarova, L. Romanova, N. Cherchenko, V. Smirnov, O. Averkov, А. Martynov, V. Vechorko, G. Gudima, D. Kudlay, R. Khaitov, M. Khaitov","doi":"10.33029/0206-4952-2022-43-1-18-32","DOIUrl":"https://doi.org/10.33029/0206-4952-2022-43-1-18-32","url":null,"abstract":"Introduction. Mass vaccination of the population against SARS-CoV-2 in Russia and abroad has been going on for more than 2 years. Various types of vaccines are used for vaccination (vector vaccines, RNA vaccines, whole-virion vaccines). The first in the world was registered the Russian vector vaccine «Gam-COVID-Vac» («Sputnik V»), which is widely used in our country, as well as in many other countries of the world. An important area of research is the monitoring of the parameters of the vaccine-induced immune response their analysis in relation to the characteristics of the immune response caused by SARSCoV-2 infection/COVID-19. Such studies are important both for assessing the intensity and duration of post-vaccination immunity, and for improving strategies for immunoprophylaxis and immunotherapy of coronavirus infection. The article presents the results of a study of the humoral immune response in patients with COVID-19 and vaccinated with «Sputnik V» in the period from autumn 2020 till the present time. The aim of the work - a comparative study of the humoral immune response to SARSCoV-2 infection and vaccination against COVID-19. Material and methods. The content of antibodies against SARS-CoV-2 S- and N-proteins was studied in 449 blood serum samples of men and women (age 25-65 years). 5 groups of samples were formed: suffered from COVID-19 of mild and moderate severity, at different times after recovery (262 samples);immunized with the «Sputnik V» vaccine, at different times after injection of the 2nd component of «Sputnik V» (104 samples);suffered from COVID-19 of mild and moderate severity, and then vaccinated with «Sputnik V» (53 samples);vaccinated with «Sputnik V», and then suffered with COVID-19 (12 samples);revaccinated with the vaccine «Sputnik Light» (18 samples). Results. To assess the content of IgG antibodies to S-protein and to N-protein of SARSCoV-2 in human blood sera, an EIA diagnostic system was developed further certified by the Ministry of Health of Russian Federation. In people suffered COVID-19 in 90 % of cases the positive levels of IgG antibodies to SARS-CoV-2 S-protein persist 9 months after recovery, while the proportion of potential plasma donors and material for obtaining intravenous immunoglobulin with a high content of IgG antibodies to S-protein 1 month after the disease is 20 %. In 76 % of people vaccinated with «Sputnik V» high levels of IgG antibodies to S-protein are detected within 6 months after the course of vaccination. The content of IgG antibodies to S-protein in the blood sera of persons suffered COVID-19, and then 6 months after recovery vaccinated with the 1st component of the vaccine «Sputnik V» in 100 % of cases was high with a positivity coefficient above 8.1, regardless of the initial value, already on 7 and 21 days after injection. In persons vaccinated with «Sputnik V» and then passed COVID-19, a high content of S-specific IgG antibodies is observed in 100 % of cases. The examination of vacci","PeriodicalId":38750,"journal":{"name":"Immunologiya","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69481897","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Interaction of dendritic cells with microorganisms capable of colonizing the intestine 树突状细胞与能够定植肠道的微生物的相互作用
Q4 Immunology and Microbiology Pub Date : 2022-01-01 DOI: 10.33029/0206-4952-2022-43-4-412-422
V. Talayev, I. Zaichenko, M. Svetlova, E. Voronina, O. Babaykina, I. Soloveva, I. Belova, A. G. Tochilina
{"title":"Interaction of dendritic cells with microorganisms capable of colonizing the intestine","authors":"V. Talayev, I. Zaichenko, M. Svetlova, E. Voronina, O. Babaykina, I. Soloveva, I. Belova, A. G. Tochilina","doi":"10.33029/0206-4952-2022-43-4-412-422","DOIUrl":"https://doi.org/10.33029/0206-4952-2022-43-4-412-422","url":null,"abstract":"","PeriodicalId":38750,"journal":{"name":"Immunologiya","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69481926","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Clinical and immunological characteristics of the postcovid period in patients with moderate-severe COVID-19 who received therapy with the inclusion of an IL-6 receptor antagonist 接受IL-6受体拮抗剂治疗的中重度COVID-19患者的临床和免疫学特征
Q4 Immunology and Microbiology Pub Date : 2022-01-01 DOI: 10.33029/0206-4952-2022-43-5-606-614
L. Sizyakina, N. Skripkina, E. Antonova, D. Sizyakin
Introduction. Significant progress in clinical research has led to a better understanding of the pathogenesis of COVID-19, contributing to its more effective therapy. The revealed key role of IL-6 in the development and intensification of the <>, which has received reliable pathophysiological and pharmacological justification, supports the use of therapeutic strategies aimed at IL-6 or its receptor. Nevertheless, the changes that occur in the immune system after COVID-19 are of interest for a better understanding of the mechanisms of the formation of postcovid syndrome in patients receiving therapy with the inclusion of IL-6 receptor antagonists, its pathogenesis and the search for targets for further therapeutic effects. The aim of the study - to study the clinical and immunological parameters of patients who underwent a moderate-severe variant of COVID-19 and received therapy with the inclusion of IL-6 receptor antagonist during treatment and 6 months after discharge/recovery. Material and methods. 30 hospitalized patients were examined with the diagnosis: COVID-19, moderate-severe form;complication: bilateral polysegmental pneumonia. The comparison group consisted of practically healthy donors (30 people). The dynamics of laboratory parameters (general clinical, biochemical and immunological) were evaluated against the background of therapy with IL-6 blockers at discharge, as well as 6 months after discharge from the hospital, in addition, the quality of life was assessed 6 months after the COVID-19. Results. Postcovid syndrome in patients who have undergone COVID-19 in a moderate-severe form manifests itself in a number of symptoms - decreased appetite, weakness, sleep disorders, depression, headache, shortness of breath, cough, tachycardia, dizziness. In addition, there is an exacerbation of chronic diseases that requires correction in planned therapy. 6 months after discharge from the hospital, there is an increase in CRP and fibrinogen levels, which most likely also reflects the deterioration of the course of concomitant pathology. There is an increase in the level of T-lymphocytes, as well as a decrease in the level of B-lymphocytes. Conclusion. Patients who had COVID-19 require dynamic follow-up. In patients with a moderate-severe form of COVID-19 who received complex therapy with the inclusion of monoclonal antibodies to IL-6 receptors, dexamethasone, antiviral therapy, anticoagulants, oxygen therapy, there are dysregulatory processes in the immune system that persist 6 months after recovery. Copyright © 2022 Meditsina Publishers. All rights reserved.
介绍。临床研究取得重大进展,加深了对新冠肺炎发病机制的认识,有助于提高治疗效果。IL-6在>发育和增强中的关键作用已得到可靠的病理生理学和药理学证明,支持使用针对IL-6或其受体的治疗策略。然而,COVID-19后免疫系统发生的变化对于更好地理解接受IL-6受体拮抗剂治疗的患者COVID-19后综合征的形成机制、发病机制和寻找进一步治疗效果的靶点具有重要意义。本研究的目的是研究在治疗期间和出院/康复后6个月接受含IL-6受体拮抗剂治疗的中重度COVID-19变异型患者的临床和免疫学参数。材料和方法。对30例住院患者进行检查,诊断为:COVID-19,中重度;并发症:双侧多节段性肺炎。对照组由实际健康的捐赠者(30人)组成。以IL-6阻滞剂治疗为背景,评估出院时和出院后6个月的实验室参数(一般临床、生化和免疫学)动态,并评估新冠肺炎后6个月的生活质量。结果。感染COVID-19的中重度患者的COVID-19后综合征表现为许多症状:食欲减退、虚弱、睡眠障碍、抑郁、头痛、呼吸短促、咳嗽、心动过速、头晕。此外,慢性病的恶化需要在计划治疗中加以纠正。出院6个月后,CRP和纤维蛋白原水平升高,这很可能也反映了伴随病理病程的恶化。t淋巴细胞水平升高,b淋巴细胞水平降低。结论。COVID-19患者需要动态随访。在接受IL-6受体单克隆抗体、地塞米松、抗病毒治疗、抗凝剂、氧疗等综合治疗的中重度COVID-19患者中,免疫系统存在持续6个月的失调过程。版权所有©2022新浪传媒出版社。版权所有。
{"title":"Clinical and immunological characteristics of the postcovid period in patients with moderate-severe COVID-19 who received therapy with the inclusion of an IL-6 receptor antagonist","authors":"L. Sizyakina, N. Skripkina, E. Antonova, D. Sizyakin","doi":"10.33029/0206-4952-2022-43-5-606-614","DOIUrl":"https://doi.org/10.33029/0206-4952-2022-43-5-606-614","url":null,"abstract":"Introduction. Significant progress in clinical research has led to a better understanding of the pathogenesis of COVID-19, contributing to its more effective therapy. The revealed key role of IL-6 in the development and intensification of the <<cytokine storm>>, which has received reliable pathophysiological and pharmacological justification, supports the use of therapeutic strategies aimed at IL-6 or its receptor. Nevertheless, the changes that occur in the immune system after COVID-19 are of interest for a better understanding of the mechanisms of the formation of postcovid syndrome in patients receiving therapy with the inclusion of IL-6 receptor antagonists, its pathogenesis and the search for targets for further therapeutic effects. The aim of the study - to study the clinical and immunological parameters of patients who underwent a moderate-severe variant of COVID-19 and received therapy with the inclusion of IL-6 receptor antagonist during treatment and 6 months after discharge/recovery. Material and methods. 30 hospitalized patients were examined with the diagnosis: COVID-19, moderate-severe form;complication: bilateral polysegmental pneumonia. The comparison group consisted of practically healthy donors (30 people). The dynamics of laboratory parameters (general clinical, biochemical and immunological) were evaluated against the background of therapy with IL-6 blockers at discharge, as well as 6 months after discharge from the hospital, in addition, the quality of life was assessed 6 months after the COVID-19. Results. Postcovid syndrome in patients who have undergone COVID-19 in a moderate-severe form manifests itself in a number of symptoms - decreased appetite, weakness, sleep disorders, depression, headache, shortness of breath, cough, tachycardia, dizziness. In addition, there is an exacerbation of chronic diseases that requires correction in planned therapy. 6 months after discharge from the hospital, there is an increase in CRP and fibrinogen levels, which most likely also reflects the deterioration of the course of concomitant pathology. There is an increase in the level of T-lymphocytes, as well as a decrease in the level of B-lymphocytes. Conclusion. Patients who had COVID-19 require dynamic follow-up. In patients with a moderate-severe form of COVID-19 who received complex therapy with the inclusion of monoclonal antibodies to IL-6 receptors, dexamethasone, antiviral therapy, anticoagulants, oxygen therapy, there are dysregulatory processes in the immune system that persist 6 months after recovery. Copyright © 2022 Meditsina Publishers. All rights reserved.","PeriodicalId":38750,"journal":{"name":"Immunologiya","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69482642","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The content of platelet-leukocyte coaggregates in the peripheral blood of healthy children of different ages 不同年龄健康儿童外周血血小板-白细胞共聚集体的含量
Q4 Immunology and Microbiology Pub Date : 2022-01-01 DOI: 10.33029/0206-4952-2022-43-6-702-713
Ye.N. Bogomyagkova, A. Solpov, P. Tereshkov, N.G. Trushina, Y. Vitkovskiy
{"title":"The content of platelet-leukocyte coaggregates in the peripheral blood of healthy children of different ages","authors":"Ye.N. Bogomyagkova, A. Solpov, P. Tereshkov, N.G. Trushina, Y. Vitkovskiy","doi":"10.33029/0206-4952-2022-43-6-702-713","DOIUrl":"https://doi.org/10.33029/0206-4952-2022-43-6-702-713","url":null,"abstract":"","PeriodicalId":38750,"journal":{"name":"Immunologiya","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69482823","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mast cell involvement in physiological and preeclampsia complicated pregnancy 肥大细胞参与生理性和子痫前期妊娠
Q4 Immunology and Microbiology Pub Date : 2022-01-01 DOI: 10.33029/0206-4952-2022-43-6-736-745
I. M. Bogdanova, K. Artemieva, M. N. Boltovskaya, M. Kondashevskaya, N. V. Nizyaeva
{"title":"Mast cell involvement in physiological and preeclampsia complicated pregnancy","authors":"I. M. Bogdanova, K. Artemieva, M. N. Boltovskaya, M. Kondashevskaya, N. V. Nizyaeva","doi":"10.33029/0206-4952-2022-43-6-736-745","DOIUrl":"https://doi.org/10.33029/0206-4952-2022-43-6-736-745","url":null,"abstract":"","PeriodicalId":38750,"journal":{"name":"Immunologiya","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69482878","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effects of interaction between circulating CD4+CCR6+ T cells and B-lymphocytes 循环CD4+CCR6+ T细胞与b淋巴细胞相互作用的影响
Q4 Immunology and Microbiology Pub Date : 2022-01-01 DOI: 10.33029/0206-4952-2022-43-3-266-276
V. Talayev, E. Voronina, M. Svetlova, I. Zaichenko, O. Babaykina
{"title":"Effects of interaction between circulating CD4+CCR6+ T cells and B-lymphocytes","authors":"V. Talayev, E. Voronina, M. Svetlova, I. Zaichenko, O. Babaykina","doi":"10.33029/0206-4952-2022-43-3-266-276","DOIUrl":"https://doi.org/10.33029/0206-4952-2022-43-3-266-276","url":null,"abstract":"","PeriodicalId":38750,"journal":{"name":"Immunologiya","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69481758","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The influence of respiratory hypoxic gas mixtures (oxygen-nitrogen and oxygen-nitrogen-argon) in a pressure chamber on the state of the human cellular immunity 压力室呼吸低氧气体混合物(氧-氮和氧-氮-氩)对人体细胞免疫状态的影响
Q4 Immunology and Microbiology Pub Date : 2022-01-01 DOI: 10.33029/0206-4952-2022-42-6-643-653
E. A. Lysenko, V. A. Shmarov, M. Rykova, E. Antropova, O. Kutko, S. Shulgina, K. Orlova, E.A. Zhirova, A. Sadova, D. D. Vlasova, S. Ponomarev
{"title":"The influence of respiratory hypoxic gas mixtures (oxygen-nitrogen and oxygen-nitrogen-argon) in a pressure chamber on the state of the human cellular immunity","authors":"E. A. Lysenko, V. A. Shmarov, M. Rykova, E. Antropova, O. Kutko, S. Shulgina, K. Orlova, E.A. Zhirova, A. Sadova, D. D. Vlasova, S. Ponomarev","doi":"10.33029/0206-4952-2022-42-6-643-653","DOIUrl":"https://doi.org/10.33029/0206-4952-2022-42-6-643-653","url":null,"abstract":"","PeriodicalId":38750,"journal":{"name":"Immunologiya","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69481786","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Immunologiya
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
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
×
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
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