Interferon profile of the mucosal immunity in women with papillomavirus infection

E. Markelova, M. S. Tulupova, T. Nevezhkina, L. S. Matyushkina, M. Chernikova, S. Knysh
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引用次数: 0

Abstract

Papillomaviruses are a group of DNA viruses belonging to the Papillomavirida family. These viruses provoke pathological conditions manifesting with inflammation, exophytic masses, carcinogenesis, reproductive and perinatal disorders. Immune status is an essential factor de-termining the severity and duration of inflammatory diseases, the course of latent viral infections, including papillomavirus infection (PVI). The human immune system prevents the persistence, reactivation, and development of PVI clinical presentations. The cellular immune response is realized under the control of interferons (IFNs). Today, no complex studies on type 1, 2, or 3 IFNs in the cervical mucus of women with PVI associated with herpesvirus and chlamydia infec-tions are available. Aim: to compare IFN profile of mucosal immunity in women with PVI associated with herpesvirus and chlamydia infections. Patients and Methods: this study enrolled 149 women aged 25–44. Women were divided into four groups. Group 1 included women with PVI only (n=21). Group 2 included women with PVI and herpesvirus infection (n=47). Group 3 included women with PVI and chlamydia infec-tions (n=39). Group 4 included controls (n=30). Complex outpatient clinical laboratory examina-tion included clinical functional, biochemical, and immunological tests to detail pathophysiolog-ical mechanisms of urogenital PVIs. IFN (IFN-β, IFN-γ, IFN-λ1/IL-29, IFN-λ3/IL-28B) levels in the cervical mucus were measured by ELISA. Results: in all groups, IFN-λ3 and IFN-γ deficiencies were detected. In PVI, IFN-γ deficiency prevailed. In PVI associated with herpesvirus infection, IFN-λ3 deficiency prevailed. In PVI associated with chlamydia infection, a severe IFN-β deficiency was revealed. Conclusion: these patterns demonstrate a relevant role of the interferon arm of the im-mune response in the pathogenesis of isolated PVI and PVI associated with herpesvirus and chlamydia infections. These alterations in mucosal immunity support the prescription of immu-notherapy for these infections. KEYWORDS: human papillomavirus, herpesvirus infection, chlamydia infection, interferons, immune system, cervical mucus, mucosal immunity. FOR CITATION: Markelova E.V., Tulupova M.S., Nevezhkina T.A. et al. Interferon profile of the mucosal immunity in women with papillomavirus infection. Russian Medical Inquiry. 2022;6(2):67–71 (in Russ.). DOI: 10.32364/2587-6821-2022-6-2-67-71.
乳头瘤病毒感染妇女粘膜免疫的干扰素谱分析
乳头瘤病毒是一组属于乳头瘤病毒科的DNA病毒。这些病毒引起的病理状况表现为炎症、外生性肿块、致癌、生殖和围产期疾病。免疫状态是决定炎症性疾病的严重程度和持续时间,潜伏病毒感染的过程,包括乳头瘤病毒感染(PVI)的重要因素。人体免疫系统阻止PVI临床表现的持续、再激活和发展。细胞免疫应答是在干扰素(ifn)的控制下实现的。目前,对于与疱疹病毒和衣原体感染相关的PVI患者宫颈粘液中1型、2型或3型ifn的复杂研究尚无。目的:比较与疱疹病毒和衣原体感染相关的PVI妇女粘膜免疫的IFN谱。患者和方法:本研究招募了149名年龄在25-44岁之间的女性。女性被分成四组。第1组仅包括患有PVI的女性(n=21)。第2组包括伴有PVI和疱疹病毒感染的女性(n=47)。第3组包括合并PVI和衣原体感染的女性(n=39)。第4组包括对照组(n=30)。复杂的门诊临床实验室检查包括临床功能、生化和免疫学检查,以详细了解泌尿生殖器PVIs的病理生理机制。ELISA法检测宫颈黏液中IFN (IFN-β、IFN-γ、IFN-λ1/IL-29、IFN-λ3/IL-28B)水平。结果:各组均检测到IFN-λ3和IFN-γ缺乏。在PVI中,IFN-γ缺乏普遍存在。在与疱疹病毒感染相关的PVI中,IFN-λ3缺乏普遍存在。在衣原体感染相关的PVI中,发现严重的IFN-β缺乏。结论:这些模式表明免疫-免疫反应的干扰素臂在分离的PVI和与疱疹病毒和衣原体感染相关的PVI发病机制中的相关作用。这些粘膜免疫的改变支持了针对这些感染的免疫治疗处方。关键词:人乳头瘤病毒,疱疹病毒感染,衣原体感染,干扰素,免疫系统,宫颈粘液,粘膜免疫。引用本文:Markelova e.v., Tulupova m.s., Nevezhkina T.A.等。乳头瘤病毒感染妇女粘膜免疫的干扰素谱分析。俄罗斯医学调查。2022;6(2):67-71(俄文)。DOI: 10.32364 / 2587-6821-2022-6-2-67-71。
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