Kollabathula Siri Sri, Venkatachalam Konakanchi, Susmitha Divya Kethireddi, Guruprasad Patnala, Nayar Pallapati Anila Sunandini
Department of Dermatology, Venereology and Leprosy, Andhra Medical College, Visakhapatnam, Andhra Pradesh, India.
Department of Dermatology, Venereology and Leprosy, Government Medical College, Srikakulam, Andhra Pradesh, India.
Indian Dermatol Online J. 2024 Apr 23;15(3):449-453. doi: 10.4103/idoj.idoj_742_23. eCollection 2024 May-Jun.
Thymic stromal lymphopoietin (TSLP) is a cytokine initially implicated to be associated with allergic disorders inducing Th2 response. Emerging studies have shown that TSLP is also involved in autoimmune diseases. In psoriasis, TSLP acts in synergy with T cell-derived CD40L to promote the release of IL-23 from dendritic cells. IL-23 is responsible for the inappropriate immune reaction and keratinocyte proliferation in psoriasis. Targeting TSLP could be a novel therapeutic approach in the treatment of psoriasis.
To compare the serum levels of TSLP between patients with psoriasis and healthy individuals.
A prospective hospital-based case-control study was carried out on 38 patients with psoriasis. The severity of psoriasis was graded into mild, moderate, and severe according to PASI. A total of 30 healthy individuals with matched age and sex were taken as controls. 5 ml of venous blood was collected, centrifuged, and the collected serum was stored at -80°C until quantitative assessment by sandwich enzyme-linked immunosorbent assay (ELISA) technique.
TSLP has been found to be significantly elevated in the sera of cases (0.1380178 pg/ml) than in controls (0.1125974 pg/ml). There was also a significant proportionate increase in the mean TSLP with the mean PASI score.
The sample size was small and we could not follow-up the cases to study the changes in TSLP levels with remission of the lesions.
We found that serum TSLP was elevated in psoriasis patients and correlated with disease severity, indicating a possible pathogenetic role.
胸腺基质淋巴细胞生成素(TSLP)是一种细胞因子,最初被认为与诱导Th2反应的过敏性疾病有关。新兴研究表明,TSLP也参与自身免疫性疾病。在银屑病中,TSLP与T细胞衍生的CD40L协同作用,促进树突状细胞释放IL-23。IL-23负责银屑病中不适当的免疫反应和角质形成细胞增殖。靶向TSLP可能是治疗银屑病的一种新的治疗方法。
比较银屑病患者和健康个体血清中TSLP水平。
对38例银屑病患者进行了一项基于医院的前瞻性病例对照研究。根据银屑病面积和严重程度指数(PASI)将银屑病严重程度分为轻度、中度和重度。共30名年龄和性别匹配的健康个体作为对照。采集5ml静脉血,离心,收集的血清储存在-80°C直至通过夹心酶联免疫吸附测定(ELISA)技术进行定量评估。
发现病例组血清中TSLP(0.1380178 pg/ml)明显高于对照组(0.1125974 pg/ml)。平均TSLP也随平均PASI评分显著成比例增加。
样本量小,我们无法对病例进行随访以研究随着皮损缓解TSLP水平的变化。
我们发现银屑病患者血清TSLP升高且与疾病严重程度相关,表明其可能具有致病作用。