The Role of NLRP3 Inflammasome in the Pathogenesis of Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis.

Medical research archives Pub Date : 2024-01-01 Epub Date: 2024-01-30 DOI:10.18103/mra.v12i1.4939
Mallika Shekhar, Omer Iqbal, Adarsh Dharan, Hanin El-Khateeb, Kavya Jatavallabhula, Ping Bu, Charles Bouchard
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Abstract

Stevens Johnson Syndrome/Toxic Epidermal Necrolysis (SJS/TEN) are mainly drug-induced severe cutaneous adverse reactions with increased mortality. It also involves the eyes causing ocular surface disease leading to visual impairment and blindness. The role of NLRP3 Inflammasome in causing ocular surface disease and keratinocyte apoptosis is not fully explored. This study is focused on determining the role of NLRP3 Inflammasome in the pathogenesis of Stevens Johnson Syndrome/Toxic Epidermal Necrolysis. The NLRP3 Inflammasome plays a crucial role in the pathogenesis of Stevens Johnson Syndrome/Toxic Epidermal Necrolysis and may correlate with the degree of severity of skin detachment and ocular surface disease. This study looked at the expression of the NLRP3 Inflammasome in the skin of patients with biopsy confirm Stevens Johnson Syndrome/Toxic Epidermal Necrolysis compared to the lichen planus and normal controls by immunohistochemistry as well as observing the mitochondrial function of platelets challenged with plasma from patients with Stevens Johnson Syndrome/Toxic Epidermal Necrolysis and Normal Human Plasma using Agilent Seahorse XF Analyzer. Under a current, Loyola IRB approved protocol, 12 collected and archived unstained slides of skin and blood plasma samples from patients with biopsy confirmed Stevens Johnson Syndrome/Toxic Epidermal Necrolysis was used for this study. Immunohistochemical analysis was performed using anti-NLRP3 antibodies followed by imaging on a Delta Vision microscope. The precise roles of cytokines and chemokine receptors in severity of skin detachment has not been completely studied. The identification of the roles of NLRP3 in Stevens Johnson Syndrome/Toxic Epidermal Necrolysis would bridge the gaps in the basic understanding regarding the pathogenesis of this disease spectrum. NLRP3 Inflammasome is a potential therapeutic target and its inhibition by phytochemicals may be appropriate effective treatment strategies in the management of this condition.

NLRP3 炎症球在史蒂文斯-约翰逊综合征/毒性表皮坏死溶解症发病机制中的作用
史蒂文斯-约翰逊综合征/毒性表皮坏死溶解症(SJS/TEN)主要是由药物引起的严重皮肤不良反应,死亡率较高。它还会累及眼睛,引起眼表疾病,导致视力损伤和失明。NLRP3 炎症小体在引起眼表疾病和角质细胞凋亡中的作用尚未得到充分探讨。本研究的重点是确定 NLRP3 炎酶体在史蒂文斯-约翰逊综合征/毒性表皮坏死溶解症发病机制中的作用。NLRP3 炎症体在史蒂文斯-约翰逊综合征/毒性表皮坏死症的发病机制中起着至关重要的作用,可能与皮肤脱落和眼表疾病的严重程度相关。本研究通过免疫组化方法观察了活检证实的史蒂文斯-约翰逊综合征/毒性表皮坏死症患者皮肤中 NLRP3 炎症小体的表达情况,并与扁平苔藓和正常对照组进行了比较,还使用安捷伦海马 XF 分析仪观察了用史蒂文斯-约翰逊综合征/毒性表皮坏死症患者血浆和正常人血浆挑战血小板的线粒体功能。根据洛约拉研究所(Loyola IRB)批准的现行方案,本研究使用了从活检证实的史蒂文斯-约翰逊综合征/中毒性表皮坏死症患者身上采集并存档的 12 张未经染色的皮肤和血浆样本切片。使用抗 NLRP3 抗体进行免疫组化分析,然后在 Delta Vision 显微镜上成像。细胞因子和趋化因子受体在皮肤脱落严重程度中的确切作用尚未完全研究清楚。确定 NLRP3 在史蒂文斯-约翰逊综合征/毒性表皮坏死溶解症中的作用将弥补对该疾病谱发病机制的基本认识上的差距。NLRP3 炎症小体是一个潜在的治疗靶点,植物化学物质对它的抑制可能是治疗这种疾病的适当有效的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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