Patients with congenital ichthyosis show differential activation of IL-23/Th17 pathway among various disease subtypes - A single-centre experience.

IF 3.4 4区 医学 Q2 DERMATOLOGY
Anoop Kumar, Rahul Mahajan, Niharika Srivastava, Shirin Bakshi, Laveena Kaushal, Adil Karim, Vinod Kumar, Dipankar De, Sanjeev Handa, Biman Saikia
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引用次数: 0

Abstract

Background Congenital ichthyosis is a rare genetic skin condition characterised by aberrant keratinisation. This study focused on assessing the differential expression of Th17-related cytokines in different subtypes of ichthyosis and its correlation with clinical features. Aim We aimed to compare the gene expression of Th17-related genes and serum levels of IL-17 and IL-23 cytokines of the ichthyosis subgroups in the Indian population. Methods We analysed blood and skin specimens from consecutively diagnosed patients with congenital ichthyosis along with age/sex-matched healthy controls using reverse transcription-polymerase chain reaction (RT-PCR), enzyme-linked immunosorbent assay (ELISA), as well as immunohistochemistry (IHC) for Th17/IL-23 pathway genes. Additionally, IFN-γ (Th1), IL-4 (Th2), and IL-17A (Th17)-dominant cell populations were measured using flow cytometry. Clinical severity was assessed using measures including the overall ichthyosis score (ICH score), which integrates erythema (E), scaling (S), and body surface area (BSA) scores. Results This study analysed interleukins in 48 congenital ichthyosis patients and 34 controls. We observed a significant upregulation of IL-17A and IL-23 in all patients, particularly autosomal recessive congenital ichthyosis (ARCI), X-linked recessive ichthyosis (XLRI), and Netherton syndrome (NS) subtypes. Similarly, serum levels of IL-17A were significantly augmented in all ichthyosis subtypes, with ARCI showing the highest increase. Whereas, an increase in IL-23 was only detected in ARCI. NS patients had significantly increased IL-22 levels. Limitations Our study included small sample size and lack of mRNA and cytokines expression in skin biopsy samples. Conclusion The study highlighted significant immunological alterations in interleukins associated with the Th17 pathway in different subtypes of congenital ichthyosis.

先天性鱼鳞病患者在不同疾病亚型中表现出IL-23/Th17通路的不同激活——单中心经验
背景:先天性鱼鳞病是一种罕见的遗传性皮肤病,其特征是异常的角化。本研究旨在探讨th17相关细胞因子在鱼鳞病不同亚型中的表达差异及其与临床特征的相关性。目的比较印度人群鱼鳞病亚群中th17相关基因的表达和血清中IL-17和IL-23细胞因子的水平。方法采用逆转录聚合酶链反应(RT-PCR)、酶联免疫吸附试验(ELISA)和免疫组化(IHC)检测Th17/IL-23通路基因,对连续确诊的先天性鱼鳞病患者和年龄/性别匹配的健康对照者的血液和皮肤标本进行分析。此外,利用流式细胞术检测IFN-γ (Th1)、IL-4 (Th2)和IL-17A (Th17)优势细胞群。临床严重程度的评估方法包括总体鱼鳞病评分(ICH评分),该评分综合了红斑(E)、鳞屑(S)和体表面积(BSA)评分。结果本研究分析了48例先天性鱼鳞病患者和34例对照组的白细胞介素水平。我们观察到IL-17A和IL-23在所有患者中显著上调,特别是常染色体隐性遗传先天性鱼鳞病(ARCI)、x连锁隐性鱼鳞病(XLRI)和内瑟顿综合征(NS)亚型。同样,血清IL-17A水平在所有鱼鳞病亚型中均显著升高,其中ARCI的升高幅度最大。而IL-23仅在ARCI中检测到升高。NS患者IL-22水平明显升高。本研究样本量小,皮肤活检样本中缺乏mRNA和细胞因子表达。结论本研究强调了先天性鱼鳞病不同亚型中与Th17通路相关的白细胞介素的免疫学改变。
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来源期刊
CiteScore
2.10
自引率
10.30%
发文量
247
审稿时长
6-12 weeks
期刊介绍: The Indian Association of Dermatologists, Venereologists & Leprologists (IADVL) is the national association of Indian medical specialists who manage patients with skin disorders, sexually transmitted infections (STIs) or leprosy. The current member strength of the association is about 3800. The association works for the betterment of the specialty by holding academic meetings, printing a journal and publishing a textbook. The IADVL has several state branches, each with their own office bearers, which function independently within the constitution of the IADVL. Established in 1940, the Indian Journal of Dermatology, Venereology and Leprology (IJDVL, ISSN 0378-6323) is the official publication of the IADVL (Indian Association of Dermatologists, Venereologists and Leprologists).
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