大麻素对 HIV-1 感染中炎性信号转导的影响。

NeuroImmune pharmacology and therapeutics Pub Date : 2023-03-25 Epub Date: 2023-02-23 DOI:10.1515/nipt-2023-0002
Alice K Min, Aislinn M Keane, Matthew Paltiel Weinstein, Talia H Swartz
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摘要

1 型人类免疫缺陷病毒(HIV-1)是一种慢性疾病,困扰着全球 3800 多万人,目前尚无治愈方法。有效的抗逆转录病毒疗法(ART)的出现大大降低了 HIV-1 感染者(PWH)的发病率和死亡率,这要归功于持久的病毒抑制。尽管如此,HIV-1 感染者仍会经历与并发症相关的慢性炎症。虽然没有单一的已知机制可以解释慢性炎症,但有大量证据支持 NLRP3 炎症小体是一个关键的驱动因素。大量研究证明了大麻素的治疗作用,包括对 NLRP3 炎症小体的调节作用。鉴于 PWH 中大麻素的高使用率,了解大麻素在 HIV-1 相关炎性体信号转导中的交叉生物学作用具有重大意义。在此,我们将介绍有关 HIV 感染者慢性炎症、大麻素对 PWH 的治疗影响、炎症中的内源性大麻素以及 HIV-1 相关炎症的文献。我们描述了大麻素、NLRP3 炎症小体和 HIV-1 病毒感染之间的关键相互作用,这支持进一步研究大麻素在 HIV-1 感染和炎症小体信号转导中的关键作用。
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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The impact of cannabinoids on inflammasome signaling in HIV-1 infection.

Human immunodeficiency virus type 1 (HIV-1) is a chronic disease that afflicts over 38 million people worldwide without a known cure. The advent of effective antiretroviral therapies (ART) has significantly decreased the morbidity and mortality associated with HIV-1 infection in people living with HIV-1 (PWH), thanks to durable virologic suppression. Despite this, people with HIV-1 experience chronic inflammation associated with co-morbidities. While no single known mechanism accounts for chronic inflammation, there is significant evidence to support the role of the NLRP3 inflammasome as a key driver. Numerous studies have demonstrated therapeutic impact of cannabinoids, including exerting modulatory effects on the NLRP3 inflammasome. Given the high rates of cannabinoid use in PWH, it is of great interest to understand the intersecting biology of the role of cannabinoids in HIV-1-associated inflammasome signaling. Here we describe the literature of chronic inflammation in people with HIV, the therapeutic impact of cannabinoids in PWH, endocannabinoids in inflammation, and HIV-1-associated inflammation. We describe a key interaction between cannabinoids, the NLRP3 inflammasome, and HIV-1 viral infection, which supports further investigation of the critical role of cannabinoids in HIV-1 infection and inflammasome signaling.

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