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严重急性呼吸综合征冠状病毒 2 感染:NLRP3 炎性小体是否可作为预防心肺并发症的合理靶点?

SARS-CoV-2 infection: NLRP3 inflammasome as plausible target to prevent cardiopulmonary complications?

机构信息

Division of Cardiology, Istituto Nazionale Tumori - IRCCS- Fondazione G. Pascale, Naples, Italy.

出版信息

Eur Rev Med Pharmacol Sci. 2020 Sep;24(17):9169-9171. doi: 10.26355/eurrev_202009_22867.

Abstract

NLRP3 (NOD-, LRR- and pyrin domain-containing protein 3) inflammasome has recently become an intriguing target of several chronic and viral diseases. Here, we argue that targeting NLRP3 inflammasome could be a strategy to prevent cardiovascular outcomes [fulminant myocarditis, heart failure, venous thromboembolism (VTE)] and acute respiratory distress syndrome (ARDS) in patients with SARS-CoV-2 infection. We discuss the rationale for NLRP3 targeting in clinical trials as an effective therapeutic strategy aimed to improve prognosis of COVID-19, analyzing the potential of two therapeutic options (tranilast and OLT1177) currently available in clinical practice.

摘要

NLRP3(核苷酸结合寡聚化结构域样受体热蛋白结构域 3)炎性小体最近成为几种慢性和病毒性疾病的一个研究热点。在这里,我们认为靶向 NLRP3 炎性小体可能是预防 SARS-CoV-2 感染患者心血管结局(暴发性心肌炎、心力衰竭、静脉血栓栓塞症[VTE])和急性呼吸窘迫综合征(ARDS)的一种策略。我们讨论了 NLRP3 靶向治疗在临床试验中的合理性,作为一种旨在改善 COVID-19 预后的有效治疗策略,并分析了目前临床可用的两种治疗选择(曲尼司特和 OLT1177)的潜力。

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