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Effects of antiviral therapy on reducing the risk of metabolic syndrome in patients with chronic hepatitis C 抗病毒治疗对降低慢性丙型肝炎患者代谢综合征风险的作用
Pub Date : 2023-07-07 DOI: 10.22625/2072-6732-2023-15-2-132-138
A. Novikova, D. Kokorev, D. Y. Konstantinov, L. L. Popova
Aim – to evaluate the effect of direct antiviral drugs (sofosbuvir and velpatasvir) on the formation of the metabolic syndrome in patients with chronic hepatitis C with a high risk of its development 2 years after treatment.Materials and methods. 112 patients with HCV (n=112) were examined, in whom the risk of developing the metabolic syndrome was determined using a specially developed method. In 58 patients, a high risk of developing metabolic syndrome was identified. This cohort of patients was divided into two groups: group 1 (n=26) who took sofosbuvir and velpatasvir and group 2 (n=32) who did not take AVT. Patients were periodically examined and observed for 2 years. At the final stage of observation, a comparative analysis of laboratory and instrumental data was carried out in patients in two comparison groups.Results. At the start of AVT, HCV patients with a high risk of developing metabolic syndrome were found to be over-weight, moderately pronounced stage of liver fibrosis (F2 according to METAVIR), high viral load, increased transaminases, total low-density lipoprotein cholesterol, atherogenic coefficient, insulin, glucose. Two years after the etiotropic therapy in HCV patients with a high risk of developing the metabolic syndrome, normalization of blood lipid metabolism, glucose, insulin levels and a decrease in the concentration of total thyroxine were registered.Conclusion. Etiotropic therapy with direct antiviral drugs in patients with chronic hepatitis C reduces the relative risk of developing the metabolic syndrome by 6,3 times.
目的:评价直接抗病毒药物(索非布韦和维帕他韦)对慢性丙型肝炎患者治疗2年后代谢综合征形成的影响。材料和方法。对112例HCV患者(n=112)进行了检查,使用一种专门开发的方法确定了这些患者发生代谢综合征的风险。在58例患者中,发现了发生代谢综合征的高风险。该队列患者分为两组:1组(n=26)服用索非布韦和维帕他韦,2组(n=32)不服用AVT。定期检查观察2年。在观察的最后阶段,对两组患者的实验室和仪器数据进行了比较分析。在AVT开始时,发现HCV患者发生代谢综合征的高风险是超重,中度肝纤维化阶段(METAVIR为F2),高病毒载量,转氨酶升高,总低密度脂蛋白胆固醇,动脉粥样硬化系数,胰岛素,葡萄糖。对发生代谢综合征的高危HCV患者进行致病因治疗2年后,血脂代谢、葡萄糖、胰岛素水平恢复正常,总甲状腺素浓度下降。慢性丙型肝炎患者使用直接抗病毒药物的致病因治疗可使发生代谢综合征的相对风险降低6.3倍。
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引用次数: 0
In memory of Klimko N.N. 纪念克里姆科
Pub Date : 2023-07-07 DOI: 10.22625/2072-6732-2023-15-2-168-172
A. Editorial
.
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引用次数: 0
Humoral immunity to new coronavirus infection and vitamin D level in healthcare workers 医护人员对新型冠状病毒感染的体液免疫与维生素D水平
Pub Date : 2023-07-07 DOI: 10.22625/2072-6732-2023-15-2-93-104
E. Krieger, O. Samodova, I. V. Schepina, L. Shagrov, Yulia M. Zvezdina
Aim: to assess the dynamic changes of humoral immune responses against the S-protein of SARS-CoV-2 and vitamin D level in healthcare workers providing care to COVID-19 patients.Methods. Repeated cross-sectional studies were conducted with an interval of 6 months (May-December 2021) including 170 healthcare workers of infectious settings. An enzyme linked immunosorbent assay was used for the quantitative detection of immunoglobulins G to SARS-CoV-2 and the vitamin D level in the blood serum.Results. In 1.5 years after the start of the pandemic, 91.2% healthcare workers were seropositive to SARS-Co-V-2. In December 2021, this proportion became 98.8%, and the percentage of individuals with high antibodies level (>150 BAU / ml) raised from 49.4% to 77%. Increase in antibodies level induced by vaccination against SARS-CoV-2 was significantly higher in those who have had prior COVID-19 (1031 BAU/мл) compared to those previously vaccinated (367 BAU/ml). The vitamin D level was lower than reference values in 71.2% of health workers and did not correlate with the concentration of antibodies to SARS-Co-V-2.Conclusion. SARS-Co-V-2 seroprevalence among healthcare workers reached almost 100% by the end of the second year of the pandemic. A greater increase in antibodies level after vaccination was observed in healthcare workers previously infected with SARS-Co-V-2 due to formation of hybrid immunity. We did not reveal the association between the vitamin D level and the humoral immune response to SARS-Co-V-2.
目的:了解医护人员对SARS-CoV-2 s蛋白的体液免疫反应及维生素D水平的动态变化。进行了间隔6个月(2021年5月至12月)的重复横断面研究,包括170名感染环境的卫生保健工作者。采用酶联免疫吸附法定量检测血清中抗SARS-CoV-2免疫球蛋白G和维生素D水平。在大流行开始后的1.5年里,91.2%的卫生保健工作者对SARS-Co-V-2血清呈阳性。2021年12月,这一比例为98.8%,抗体水平高(>150 BAU / ml)的个体比例从49.4%上升到77%。与先前接种过疫苗的人(367 BAU/ml)相比,先前接种过COVID-19疫苗的人(1031 BAU/мл)接种SARS-CoV-2疫苗诱导的抗体水平升高明显更高。71.2%的卫生工作者维生素D水平低于参考值,且与sars - co - v抗体浓度无相关性。到大流行第二年结束时,卫生保健工作者的SARS-Co-V-2血清阳性率几乎达到100%。在以前感染过SARS-Co-V-2的卫生保健工作者中,由于形成混合免疫,在接种疫苗后抗体水平增加更大。我们没有揭示维生素D水平与对SARS-Co-V-2的体液免疫反应之间的关联。
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引用次数: 0
Unusual course of meningococcal infection with lethal outcome (brief communication) 脑膜炎球菌感染的异常病程和致死结果(简短通讯)
Pub Date : 2023-07-07 DOI: 10.22625/2072-6732-2023-15-2-165-166
V. Zinserling, Yu. V. Sukhanova, D. Gusev
We present a brief description of lethal case of meningococcal infection in 41 y old women, diagnosed by detection of Neisseria meningitidis in blood and results of histobacterioscopic study with the absence of rash and prominent mononuclear (non purulent) infiltration of soft meninges.
我们报告41岁老年妇女脑膜炎球菌感染致死病例,通过血液中脑膜炎奈瑟菌的检测和组织细菌镜检查结果诊断,没有皮疹和突出的软脑膜单核(非化脓性)浸润。
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引用次数: 0
A case of co-infection of monkeypox and herpes simplex virus type 1 猴痘和1型单纯疱疹病毒合并感染1例
Pub Date : 2023-07-07 DOI: 10.22625/2072-6732-2023-15-2-162-165
E. Venev, D. Lioznov, A. Komissarov, A. Fadeev, K. S. Komissarova, N. Yolshin, D. Gusev
The first Russian clinical case of monkeypox in combination with herpes simplex type 1 infection in a 29-year-old man who returned from Portugal is described. The protocols for sequencing the virus genome are presented. Particular attention is paid to the difficulty of diagnosing vesicular rash in patients with a suspicious history.
俄罗斯首例猴痘合并1型单纯疱疹感染的临床病例发生在一名从葡萄牙返回的29岁男子身上。提出了病毒基因组测序的方案。特别要注意的是诊断有可疑病史的病人的水疱疹的困难。
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引用次数: 0
Diagnostic and prognostic value of neuron-specific enolase and S-100 protein in pediatric viral encephalitis 神经元特异性烯醇化酶和S-100蛋白在小儿病毒性脑炎中的诊断和预后价值
Pub Date : 2023-07-07 DOI: 10.22625/2072-6732-2023-15-2-105-113
L. A. Alekseeva, N. Skripchenko, T. V. Bessonova, E. Gorelik, E. Skripchenko, A. Zhirkov, G. F. Zheleznikova, N. E. Monakhova
Objective – to study the dynamics of the level of neuron-specific enolase (NSE) and S-100 protein in blood serum and cerebrospinal fluid in children with various features of viral encephalitis course and outcome and to define their role in diagnostics and prognosis.Material and methods. 48 children aged from 1 month to 15 years were examined. Analysis of the level of NSE and S-100 protein was performed by the method of hardphase immune-enzyme analysis.Results. A reliable increase of the level of S-100 protein in blood serum was identified in comparison with the control group in both acute and reconvalescence periods. During acute period higher values of NSE in blood serum were found in children with herpesvirus encephalitis of various etiologies in comparison with varicella zoster encephalitis, and during reconvalescence period – higher values of S-100 protein. In case of the most severe course of the disease the level of NSE in cerebrospinal fluid was reliably higher in comparison with patients in severe condition. Children with convulsive syndrome demonstrated higher concentration of NSE in cerebrospinal fluid than patients without convulsions. In case of formation of stable neurologic deficiency during the disease outcome there was identified an increase of NSE concentration in blood serum in comparison with the recovered patients. It was also identified that if the values of NSE were >7.0 ng/ml, it was possible to predict unfavourable outcome of viral encephalitis with sensitivity of 61.54% and specificity of 71.43%. The highest values of neuron-specific proteins in blood serum were found in the dead patient with herpes encephalitis.Conclusion. Analysis of NSE and S-100 protein in pediatric viral encephalitis is characterized by diagnostic and prognostic significance, demonstrates their role in pathogenesis and can be used for therapy correction.
目的:研究具有不同特点的病毒性脑炎病程和结局患儿血清和脑脊液中神经元特异性烯醇化酶(NSE)和S-100蛋白水平的动态变化,并确定其在诊断和预后中的作用。材料和方法。对48名1个月至15岁的儿童进行了检查。采用硬相免疫酶法分析NSE和S-100蛋白水平。与对照组相比,急性期和恢复期血清S-100蛋白水平均有可靠的升高。不同病因的疱疹病毒脑炎患儿血清NSE水平在急性期高于水痘带状疱疹脑炎,恢复期S-100蛋白水平高于水痘带状疱疹脑炎。在病程最严重的情况下,脑脊液中NSE的水平确实高于重症患者。惊厥综合征患儿脑脊液中NSE浓度高于无惊厥的患儿。在疾病结果期间形成稳定的神经功能缺陷的情况下,与康复患者相比,血清中NSE浓度增加。如果NSE值>7.0 ng/ml,则可以预测病毒性脑炎的不良结局,敏感性为61.54%,特异性为71.43%。死亡的疱疹脑炎患者血清中神经元特异性蛋白含量最高。NSE和S-100蛋白在小儿病毒性脑炎中的分析具有诊断和预后意义,阐明了它们在发病机制中的作用,并可用于治疗纠正。
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引用次数: 0
Clinical and laboratory features of viral lower respiratory tract infections in children 儿童病毒性下呼吸道感染的临床和实验室特征
Pub Date : 2023-07-07 DOI: 10.22625/2072-6732-2023-15-2-84-92
E. Orlova, I. Babachenko, N. Tian, E. Kozyrev, L. A. Alekseeva
Purpose: to give a comparative characteristic of the clinical and laboratory manifestations of viral lower respiratory tract infections of various etiologies.Object and methods: Medical information of 385 patients, who were hospitalized in the clinic of Pediatric Research and Clinical Center for Infectious Diseases in the period from 2016 to 2022, was retrospectively analyzed. Inclusion criteria: age from 1 month to 17 years; infectious diseases of the lower respiratory tract; extraction of respiratory viral nucleic acids in nasopharyngeal swabs by polymerase chain reaction. Upon admission, all children underwent: a physical examination, an examination by an otorhinolaryngologist, a complete blood test with a leucogram, determination of the level of C-reactive protein, and, if it necessary, a chest X-ray in two projections.Results: Respiratory syncytial virus and rhinovirus dominated in the etiological structure of lower respiratory tract infection. Differences in the duration and severity of fever and manifestations of catarrhal syndrome in respiratory viral infections of various etiologies were established. Boca-virus and rhinovirus infections often caused severe damage of the lower respiratory tract with acute respiratory failure. Viral lower respiratory tract infections have such changes in the leucogram as an increase in neutrophils and band cells, which persist for 4-5 days of the disease. The severity of inflammatory changes in the haemogram depends on the etiology of the disease. The most significant changes, such as leukocytosis and an increase in the absolute count of neutrophils, were detected in adenovirus and rhinovirus infections.Conclusion: There were age and clinical features of viral lower respiratory tract infections in children. Prolonged fever and identified inflammatory changes in the hemogram, often in combination with an increase in the level of C-reactive protein, in children with viral lesions of the lower respiratory tract explain the frequency of prescribing antibacterial drugs at any stage of medical care. To select the optimal therapy tactics, it is necessary to take into account the clinical and laboratory features of respiratory viral infections in patients with diseases of the lower respiratory tract.
目的:比较不同病因的病毒性下呼吸道感染的临床和实验室表现特点。目的与方法:回顾性分析2016 - 2022年在儿科研究与传染病临床中心门诊住院的385例患者的医疗资料。纳入标准:年龄1个月~ 17岁;下呼吸道传染病;聚合酶链反应法提取鼻咽拭子呼吸道病毒核酸。入院后,所有儿童都接受了体格检查、耳鼻喉科医生的检查、含白细胞的全血检查、c反应蛋白水平的测定,如有必要,在两个突出部位进行胸部x光检查。结果:呼吸道合胞病毒和鼻病毒在下呼吸道感染的病因结构中占主导地位。不同病因的呼吸道病毒感染在发烧的持续时间和严重程度以及卡他性综合征的表现上存在差异。博卡病毒和鼻病毒感染常引起严重的下呼吸道损伤,并发急性呼吸衰竭。病毒性下呼吸道感染在白细胞图上有中性粒细胞和带细胞增加等变化,这种变化持续4-5天。血象中炎症变化的严重程度取决于疾病的病因。在腺病毒和鼻病毒感染中检测到最显著的变化,如白细胞增多和中性粒细胞绝对计数的增加。结论:儿童病毒性下呼吸道感染具有年龄和临床特点。在患有下呼吸道病毒病变的儿童中,长期发烧和血象中确定的炎症变化,通常与c反应蛋白水平升高相结合,解释了在医疗保健的任何阶段处方抗菌药物的频率。考虑下呼吸道疾病患者呼吸道病毒感染的临床和实验室特点,选择最佳的治疗策略是必要的。
{"title":"Clinical and laboratory features of viral lower respiratory tract infections in children","authors":"E. Orlova, I. Babachenko, N. Tian, E. Kozyrev, L. A. Alekseeva","doi":"10.22625/2072-6732-2023-15-2-84-92","DOIUrl":"https://doi.org/10.22625/2072-6732-2023-15-2-84-92","url":null,"abstract":"Purpose: to give a comparative characteristic of the clinical and laboratory manifestations of viral lower respiratory tract infections of various etiologies.Object and methods: Medical information of 385 patients, who were hospitalized in the clinic of Pediatric Research and Clinical Center for Infectious Diseases in the period from 2016 to 2022, was retrospectively analyzed. Inclusion criteria: age from 1 month to 17 years; infectious diseases of the lower respiratory tract; extraction of respiratory viral nucleic acids in nasopharyngeal swabs by polymerase chain reaction. Upon admission, all children underwent: a physical examination, an examination by an otorhinolaryngologist, a complete blood test with a leucogram, determination of the level of C-reactive protein, and, if it necessary, a chest X-ray in two projections.Results: Respiratory syncytial virus and rhinovirus dominated in the etiological structure of lower respiratory tract infection. Differences in the duration and severity of fever and manifestations of catarrhal syndrome in respiratory viral infections of various etiologies were established. Boca-virus and rhinovirus infections often caused severe damage of the lower respiratory tract with acute respiratory failure. Viral lower respiratory tract infections have such changes in the leucogram as an increase in neutrophils and band cells, which persist for 4-5 days of the disease. The severity of inflammatory changes in the haemogram depends on the etiology of the disease. The most significant changes, such as leukocytosis and an increase in the absolute count of neutrophils, were detected in adenovirus and rhinovirus infections.Conclusion: There were age and clinical features of viral lower respiratory tract infections in children. Prolonged fever and identified inflammatory changes in the hemogram, often in combination with an increase in the level of C-reactive protein, in children with viral lesions of the lower respiratory tract explain the frequency of prescribing antibacterial drugs at any stage of medical care. To select the optimal therapy tactics, it is necessary to take into account the clinical and laboratory features of respiratory viral infections in patients with diseases of the lower respiratory tract.","PeriodicalId":226950,"journal":{"name":"Journal Infectology","volume":"91 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-07-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"123126744","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
Effectiveness of Glecaprevir/Pibrentasvir in Patients with Chronic HCV-infection Genotypes 1 to 6 in the real-world settings in Russia (EVEREST study) Glecaprevir/Pibrentasvir在俄罗斯1 - 6基因型慢性hcv感染患者中的疗效(EVEREST研究)
Pub Date : 2023-07-06 DOI: 10.22625/2072-6732-2023-15-2-47-59
О. Sagalova, V. S. Adonieva, S. V. Zotov, D. Gusev, E. Strebkova, R. B. Galbraikh, V. Morozov, I. M. Khayertynova, I. V. Krasilnikova, I. V. Sannikova, A. Bhagat, D. O. Milenin, A. P. Efremova
Background: Glecaprevir/pibrentasvir (GLE/PIB) is the first pangenotypic ribavirin-free regimen allowing for treatment duration as short as 8 weeks for the majority of patients with chronic hepatitis C (CHC) genotypes (GT) 1 to 6. The results of clinical trials showed good tolerability of GLE/PIB and high virologic response rate (mostly >95%) among different patient populations. The main objective of this study was to determine how the efficacy and safety of GLE/PIB translates into real-world clinical settings in Russia.Materials and Methods: This was a prospective, multicenter observational study in patients with CHC who received the GLE/PIB regimen. The treatment regimen was prescribed by a physician in accordance with all applicable requirements before the enrollment in the study. Patients were observed for the duration of GLE/PIB therapy and at least for up to 12 weeks after the treatment completion. Real-world data were collected in patient records. Follow-up visits, procedures, and diagnostic methods followed physicians’ routine clinical practice.Results: Overall 161 patients were enrolled in the study in 11 study sites of them 128 patients had sufficient follow-up data to assess sustained virological response 12 weeks [i.e. ≥70 days] after the end of treatment with GLE/PIB (SVR12). Overall, 127 out of 128 patients (99.2%) achieved SVR12. Depending on treatment duration the following SVR12 rates were achieved: 98.7% in 8-week group (75/76), 100% in 12-week group (49/49) and 100% in 16-week group (3/3). One patient failed to achieve SVR, the exact reasons of failure couldn’t be established by the Investigator.Since only one patient didn’t achieve primary endpoint the following SVR12 rates were achieved in different subpopulations: 91.7% in patients with GT2 (11/12); 98.9% in non-cirrhotic patients (88/89); 99.1% in treatment-naïve patients (113/114); 99.1% in patients without HIV co-infection (116/117); 99.2% in patients younger than 65 years (120/121).On the other hand, SVR12 was achieved by all patients (100%) in the following subpopulations: patients with GT3 (n=76), GT1a (n=5), GT1b (n=29) and other GTs (n=6); cirrhotic patients (n=36) and those with unknown cirrhosis status (n=3); treatment-experienced patients (n=14); HIV/HCV co-infected patients (n=11); patients older than 65 years (n=7); and drug users (n=10).No clinically significant abnormalities in the key laboratory parameters were noted during the study. On contrary, the overall improvement of the liver enzymes was observed at SVR12 Visit. There were 3 patients with 3 adverse events (AEs): 2 cases were mild (cough and rash), and 1 case was severe and evaluated as a serious AE (hepatic decompensation). Hepatic decompensation led to the patient withdrawal from the study; this serious AE was preceded by 2 months of daily alcohol consumption and in the investigator’s opinion was not related to GLE/PIB intake. Of all AEs only rash was related to GLE/PIB administration according to in
背景:Glecaprevir/pibrentasvir (GLE/PIB)是首个无利巴韦林的泛型方案,允许大多数慢性丙型肝炎(CHC)基因型(GT) 1至6的患者治疗时间短至8周。临床试验结果显示,GLE/PIB在不同患者群体中耐受性良好,病毒学应答率高(多数>95%)。本研究的主要目的是确定GLE/PIB在俄罗斯临床环境中的有效性和安全性。材料和方法:这是一项前瞻性、多中心观察性研究,研究对象是接受GLE/PIB方案治疗的CHC患者。在研究登记前,治疗方案由医生按照所有适用的要求处方。在GLE/PIB治疗期间对患者进行观察,并在治疗完成后至少观察12周。真实世界的数据收集在患者记录中。随访、程序和诊断方法遵循医生的常规临床实践。结果:共有161名患者在11个研究地点入组,其中128名患者有足够的随访数据来评估GLE/PIB (SVR12)治疗结束后12周(即≥70天)的持续病毒学反应。总体而言,128名患者中有127名(99.2%)达到了SVR12。根据治疗时间的不同,SVR12率达到:8周组98.7%(75/76),12周组100%(49/49),16周组100%(3/3)。1例患者未能达到SVR,研究者无法确定具体原因。由于只有一名患者没有达到主要终点,不同亚群的SVR12率达到以下水平:GT2患者91.7% (11/12);非肝硬化患者占98.9% (88/89);treatment-naïve患者占99.1% (113/114);未合并HIV感染的患者占99.1% (116/117);65岁以下患者占99.2%(120/121)。另一方面,以下亚群中所有患者(100%)均达到了SVR12: GT3 (n=76)、GT1a (n=5)、GT1b (n=29)和其他GTs (n=6)患者;肝硬化患者(n=36)和肝硬化状态未知的患者(n=3);有治疗经验的患者(n=14);HIV/HCV合并感染患者(n=11);65岁以上患者(n=7);吸毒者(n=10)。研究期间未发现关键实验室参数有临床意义的异常。相反,在SVR12访问时观察到肝酶的整体改善。3例患者出现3个不良事件(AE): 2例为轻度(咳嗽、皮疹),1例为重度(肝脏失代偿)。肝脏失代偿导致患者退出研究;严重AE发生前有2个月的每日饮酒史,研究者认为与GLE/PIB摄入无关。根据研究者的意见,所有ae中只有皮疹与GLE/PIB用药有关。结论:在常规临床实践中,GLE/PIB已被证明是一种非常有效的治疗方案,适用于所有丙型肝炎病毒基因型患者,包括GT3和代偿性肝硬化患者。本研究显示的SVR12发生率与先前发表的数据完全一致。患者对该方案的耐受性良好。
{"title":"Effectiveness of Glecaprevir/Pibrentasvir in Patients with Chronic HCV-infection Genotypes 1 to 6 in the real-world settings in Russia (EVEREST study)","authors":"О. Sagalova, V. S. Adonieva, S. V. Zotov, D. Gusev, E. Strebkova, R. B. Galbraikh, V. Morozov, I. M. Khayertynova, I. V. Krasilnikova, I. V. Sannikova, A. Bhagat, D. O. Milenin, A. P. Efremova","doi":"10.22625/2072-6732-2023-15-2-47-59","DOIUrl":"https://doi.org/10.22625/2072-6732-2023-15-2-47-59","url":null,"abstract":"Background: Glecaprevir/pibrentasvir (GLE/PIB) is the first pangenotypic ribavirin-free regimen allowing for treatment duration as short as 8 weeks for the majority of patients with chronic hepatitis C (CHC) genotypes (GT) 1 to 6. The results of clinical trials showed good tolerability of GLE/PIB and high virologic response rate (mostly >95%) among different patient populations. The main objective of this study was to determine how the efficacy and safety of GLE/PIB translates into real-world clinical settings in Russia.Materials and Methods: This was a prospective, multicenter observational study in patients with CHC who received the GLE/PIB regimen. The treatment regimen was prescribed by a physician in accordance with all applicable requirements before the enrollment in the study. Patients were observed for the duration of GLE/PIB therapy and at least for up to 12 weeks after the treatment completion. Real-world data were collected in patient records. Follow-up visits, procedures, and diagnostic methods followed physicians’ routine clinical practice.Results: Overall 161 patients were enrolled in the study in 11 study sites of them 128 patients had sufficient follow-up data to assess sustained virological response 12 weeks [i.e. ≥70 days] after the end of treatment with GLE/PIB (SVR12). Overall, 127 out of 128 patients (99.2%) achieved SVR12. Depending on treatment duration the following SVR12 rates were achieved: 98.7% in 8-week group (75/76), 100% in 12-week group (49/49) and 100% in 16-week group (3/3). One patient failed to achieve SVR, the exact reasons of failure couldn’t be established by the Investigator.Since only one patient didn’t achieve primary endpoint the following SVR12 rates were achieved in different subpopulations: 91.7% in patients with GT2 (11/12); 98.9% in non-cirrhotic patients (88/89); 99.1% in treatment-naïve patients (113/114); 99.1% in patients without HIV co-infection (116/117); 99.2% in patients younger than 65 years (120/121).On the other hand, SVR12 was achieved by all patients (100%) in the following subpopulations: patients with GT3 (n=76), GT1a (n=5), GT1b (n=29) and other GTs (n=6); cirrhotic patients (n=36) and those with unknown cirrhosis status (n=3); treatment-experienced patients (n=14); HIV/HCV co-infected patients (n=11); patients older than 65 years (n=7); and drug users (n=10).No clinically significant abnormalities in the key laboratory parameters were noted during the study. On contrary, the overall improvement of the liver enzymes was observed at SVR12 Visit. There were 3 patients with 3 adverse events (AEs): 2 cases were mild (cough and rash), and 1 case was severe and evaluated as a serious AE (hepatic decompensation). Hepatic decompensation led to the patient withdrawal from the study; this serious AE was preceded by 2 months of daily alcohol consumption and in the investigator’s opinion was not related to GLE/PIB intake. Of all AEs only rash was related to GLE/PIB administration according to in","PeriodicalId":226950,"journal":{"name":"Journal Infectology","volume":"23 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"133482211","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
Changes in serotype distribution of Streptococcus pneumonia circulating among children in the Russian Federation after 13-valent pneumococcal conjugate vaccine introduction. 引入13价肺炎球菌结合疫苗后俄罗斯联邦儿童中流行的肺炎链球菌血清型分布的变化
Pub Date : 2023-07-06 DOI: 10.22625/2072-6732-2023-15-2-6-13
S. Sidorenko, Y. Lobzin, W. Rennert, E. V. Nikitina, I. Tsvetkova, V. Ageevets, E. Martens, O. Kalinogorskaya, A. Ardysheva, L. Bayazitova, A. Bikmieva, E. Bolgarova, E. A. Brzhozovska, I. Verentsova, A. A. Girina, Y. Zakharova, T. V. Illarionova, G. Isaeva, A. V. Klimashina, O. Kovalishena, T. G. Kozeeva, N. A. Mayansky, I. A. Nemirovchenko, I. V. Pozdeeva, V. Salina, N. Sokolova, L. V. Tomracheva, Yury A Tyurin, I. V. Feldblyum, I. Shirokova, S. M. Skripkovskaya, A. Aleksandrova
During a prospective multicenter non-interventional observational study, a comparative assessment was made of the serotype structure of pneumococci circulating among healthy children under the age of 5 years and children of the same age group with signs of respiratory infections in the periods 2016-2018 and 2020-2022. Data on the serotype structure of pneumococci in the period from 2016-2018 were obtained from our previous works. In 2020-2022 the study included 2066 healthy children and 603 children with respiratory infections. Streptococcus pneumoniae and their DNA were detected in nasopharyngeal swabs by classical culture and molecular methods. Typing was carried out by molecular methods. On the territory of the Russian Federation, pneumococci belonging to the serotypes included in the 13-valent vaccine are being forced out of circulation and replaced by non-vaccine serotypes. Before the introduction of mass antipneumococcal vaccination (until 2015), the 13-valent conjugate vaccine covered from 66.2% to 92% of pneumococci, after the start of mass anti-pneumococcal vaccination in the period 2016-2018, coverage decreased to 57.3%. Between 2020 and 2022, coverage was less than 40%. The main “non-vaccine” serotypes/serogroups circulating in the Russian Federation are 15AF, 11AD, 23A, 9LN and 16F.
在一项前瞻性多中心非干预性观察性研究中,对2016-2018年和2020-2022年期间5岁以下健康儿童和有呼吸道感染症状的同年龄组儿童的肺炎球菌血清型结构进行了比较评估。2016-2018年肺炎球菌血清型结构数据来源于我们之前的工作。在2020-2022年期间,该研究包括2066名健康儿童和603名呼吸道感染儿童。采用经典培养法和分子法对鼻咽拭子中肺炎链球菌及其DNA进行检测。采用分子分型方法进行分型。在俄罗斯联邦境内,属于13价疫苗所含血清型的肺炎球菌正被迫停止流通,代之以非疫苗血清型。在引入大规模抗肺炎球菌疫苗接种之前(直到2015年),13价结合疫苗的肺炎球菌覆盖率为66.2%至92%,在2016-2018年期间开始大规模抗肺炎球菌疫苗接种后,覆盖率下降至57.3%。在2020年至2022年期间,覆盖率不到40%。在俄罗斯联邦流行的主要"非疫苗"血清型/血清组是15AF、11AD、23A、9LN和16F。
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引用次数: 0
Modern concepts of the mechanisms of congenital cytomegalovirus infection development 先天性巨细胞病毒感染发展机制的现代概念
Pub Date : 2023-07-06 DOI: 10.22625/2072-6732-2023-15-2-35-46
V. Vasil’ev, N. Rogozina, I. Markin
The review presents modern information of domestic and foreign authors about possible pathogenetic mechanisms of the virus effect on the fetus in the case of cytomegalovirus infection in pregnant women. Immunosuppressive changes, which are a feature of the physiological course of pregnancy, create favorable conditions for the development of active cytomegalovirus infection. The virus’s ability to infect a wide range of cells in vivo and trigger a set of molecular mechanisms causes changes in placental cell differentiation, which plays a key role in transplant transmission. The processes of formation of chronic placental insufficiency, which leads to hypoxia of the fetus and to delay of intrauterine development, are separately highlighted. The literary data on non-specific metabolic changes of the mother and placental activation of proinflammatory cytokines (TNF-α, IL-1β, IL2, IL-6 and IL-8), which occur in cytomegalovirus infection and are of significant importance in formation of hypoxia of the fetus have been analyzed.In addition, the role of individual cells in preventing intrauterine infection is examined, namely the deciduous macrophages with antiviral activity, the deciduous natural killers and their activated toll-like receptors. The article also discusses the genetic predisposition to the development of manifest forms of EID, including the relationship of polymorphism of TLR2 and Arg753Gln genes with an increased risk of intrauterine infection of the fetus CMV.Characteristic properties of the virus are pronounced genetic diversity, the ability to life-long persistence in various human organs and tissues (secretory glands, lymphatic cells, kidneys, etc.) and replication without cell damage, as well as suppressing cellular immunity. The article describes the issues of genotyping of virus and the relationship of some genotypes with certain organ pathology in newborns.
本文综述了国内外有关孕妇巨细胞病毒感染时病毒对胎儿可能致病机制的最新研究进展。免疫抑制变化是妊娠生理过程的一个特征,为巨细胞病毒活动性感染的发展创造了有利条件。该病毒能够在体内感染多种细胞,并触发一系列分子机制,导致胎盘细胞分化发生变化,这在移植传播中起着关键作用。慢性胎盘功能不全的形成过程,导致胎儿缺氧和延迟宫内发育,分别强调。本文对巨细胞病毒感染时母体非特异性代谢变化和胎盘促炎因子(TNF-α、IL-1β、il - 2、IL-6和IL-8)激活的文献资料进行了分析,这些因子在胎儿缺氧的形成中起重要作用。此外,还研究了个体细胞在预防宫内感染中的作用,即具有抗病毒活性的乳糜巨噬细胞、乳糜自然杀伤细胞及其激活的toll样受体。本文还讨论了明显形式EID的遗传易感性,包括TLR2和Arg753Gln基因多态性与胎儿巨细胞病毒宫内感染风险增加的关系。该病毒的特点是显著的遗传多样性,能够在人体各种器官和组织(分泌腺、淋巴细胞、肾脏等)中终身存在,并在不损伤细胞的情况下进行复制,以及抑制细胞免疫。本文介绍了新生儿病毒基因分型的问题以及一些基因型与某些器官病理的关系。
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Journal Infectology
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