Content of CD4+T cell subpopulations in predicting the efficacy of biological therapy for psoriasis in children

D. Kuptsova, T. Radigina, O. Kurbatova, A. I. Materikin, R. Epishev, L. A. Opryatin, A. Khotko, N. Murashkin, S. Petrichuk
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Abstract

Psoriasis is a chronic inflammatory skin disease characterized by increased proliferation of epidermal cells, impaired keratinization and an inflammatory reaction in dermis caused by activation of T lymphocytes and synthesis of pro-inflammatory cytokines. The pathophysiology of psoriasis is also associated with a decrease in anti-inflammatory functions of immunosuppressive cells. Recently, there are more cases of development of resistance to ongoing therapy with biologics in children, requiring cancellation of drug or its replacement. The aim of the study was to evaluate the content of T helper subpopulations in prognosis of effectiveness of biologics in children with psoriasis. Immunophenotyping of T helper populations was performed in 110 children with psoriasis vulgaris before appointment of biologics, at 16 and 52 weeks. Age of children ranged from 6 to 18 years. Severity of psoriasis and effectiveness of therapy were assessed by index PASI, which varied 0-68. Content of Tregs, Thact and Th17 was determined by flow cytometry. In group with a sufficient effect of biologics, a decrease in PASI was obtained, both at week 16 of therapy (p = 0.000) and by year of treatment, p = 0.017. In children with psoriasis, regardless of duration and effectiveness of biologics, percentage of Thact was increased relative to normal values. In group 1 before prescription of biologics was increased percentage of Thact (p = 0.005) and Th17 (p = 0.001). Analysis of dynamics of content of small populations of T helper during 1 year of use of biologics in children with different efficacy of therapy showed that significant changes were found in content of Th17 and Treg, as well as their Th17/Treg. ROC analysis showed that when Th17 deviation was above 53%, Thact above 181% and Th17/Treg above 2.6 before biologics were prescribed, insufficient efficacy of therapy could be expected in 75% of cases by year. By the end of induction course, with a Th17 deviation above 102% and a Th17/Treg above 2.6, probability of ineffective treatment was already 82%. The study shows the informative value of assessment of Thact before appointment of biologics, dynamics of Th17 by the end of induction course and Treg after 16 weeks of therapy in prognosis of effectiveness of biologics in children with psoriasis.
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CD4+T细胞亚群的含量预测儿童银屑病生物治疗的疗效
银屑病是一种慢性炎症性皮肤病,其特征是表皮细胞增殖增加、角化受损以及由T淋巴细胞激活和促炎细胞因子合成引起的真皮炎症反应。牛皮癣的病理生理也与免疫抑制细胞的抗炎功能下降有关。最近,越来越多的儿童对正在进行的生物制剂治疗产生耐药性,需要取消药物或替代药物。本研究的目的是评估辅助性T细胞亚群的含量对银屑病儿童生物制剂疗效预后的影响。对110例寻常型银屑病患儿在16周和52周使用生物制剂前进行T辅助人群免疫分型。儿童的年龄从6岁到18岁不等。用PASI指数(0-68)评价银屑病的严重程度和治疗效果。流式细胞术检测Tregs、Thact和Th17的含量。在生物制剂效果充分的组中,PASI在治疗第16周(p = 0.000)和治疗后一年(p = 0.017)均有所下降。在患有牛皮癣的儿童中,无论生物制剂的持续时间和有效性如何,Thact的百分比相对于正常值都有所增加。1组患者在开生物制剂前Thact和Th17百分比均升高(p = 0.005), Th17百分比升高(p = 0.001)。通过对不同疗效儿童使用生物制剂1年期间小群体辅助性T细胞含量的动态分析,发现Th17和Treg含量及其Th17/Treg含量发生了显著变化。ROC分析显示,在使用生物制剂前,Th17偏差大于53%,Thact大于181%,Th17/Treg大于2.6,按年计算,75%的病例可预期治疗效果不足。诱导疗程结束时,Th17偏差大于102%,Th17/Treg大于2.6,治疗无效的概率已达82%。本研究显示,在预约生物制剂前评估Thact、诱导疗程结束时Th17的动态以及治疗16周后评估Treg对银屑病儿童生物制剂疗效预后的信息价值。
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来源期刊
Medical Immunology (Russia)
Medical Immunology (Russia) Medicine-Immunology and Allergy
CiteScore
0.70
自引率
0.00%
发文量
88
审稿时长
12 weeks
期刊介绍: The journal mission is to promote scientific achievements in fundamental and applied immunology to various medical fields, the publication of reviews, lectures, essays by leading domestic and foreign experts in the field of fundamental and experimental immunology, clinical immunology, allergology, immunodiagnostics and immunotherapy of infectious, allergy, autoimmune diseases and cancer.
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