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Biologics targeting IL-17 and IL-23 maintain stability in patients with psoriasis during COVID-19 infection: a case-control study

银屑病 医学 2019年冠状病毒病(COVID-19) 白细胞介素17 乌斯特基努马 皮肤病科 大流行 肿瘤坏死因子α 内科学 白细胞介素 疾病 耐火材料(行星科学) 免疫学 阿达木单抗 炎症 细胞因子 传染病(医学专业) 物理 天体生物学
作者
Dawei Huang,Yingyuan Yu,Jiajing Lu,Fei Tan,Yujun Shi
出处
期刊:Frontiers in Medicine [Frontiers Media SA]
卷期号:10
标识
DOI:10.3389/fmed.2023.1280965
摘要

Psoriasis is a chronic and refractory skin disease. The emergence of biologics provides more options for the treatment of psoriasis, but the COVID-19 pandemic poses challenges for the management of psoriasis.The purpose of this study was to investigate the effect of different biologics on the stabilization of psoriasis during COVID-19 infection in China.This is a single-center, observational, retrospective, case-control study. Using our database, we conducted a remote dermatologic study by means of questionnaire follow-up or telephone follow-up to collect general information of patients, information related to COVID-19 infection and conditions of psoriasis for comparison and further analysis between groups.Our study ultimately included 274 patients for analysis. We found that the patients in this collection had mild symptoms of COVID-19 infection, and only 13 of them needed to go to the hospital for medical treatment. Further studies found that in biologics, relative to tumor necrosis factor-α inhibitors (TNF-αi), interleukin-17 inhibitors (IL-17i) and interleukin-23 inhibitors (IL-23i) are both protective factors in flare-up of psoriasis [IL-17i: OR (95% CI) = 0.412 (0.189-0.901); IL-23i: OR (95% CI) = 0.291 (0.097-0.876)]. In addition, we also found that the proportion of people with increased psoriasis developing long COVID-19 increased, and we speculated that increased psoriasis may be a potential risk factor for long COVID-19.Our study showed that the use of IL-17i and IL-23i was a protective factor for psoriasis compared with TNF-αi, and could keep the psoriasis stable.

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