4.5 Review

Therapeutic Potential of Targeting the NLRP3 Inflammasome in Rheumatoid Arthritis

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INFLAMMATION
卷 46, 期 3, 页码 835-852

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SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10753-023-01795-5

关键词

rheumatoid arthritis; NLRP3; inflammasome; IL-1 beta

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The NOD-like receptor family pyrin domain-containing 3 (NLRP3) inflammasome is a cytoplasmic multiprotein complex involved in innate immune response. Its aberrant activation is associated with various inflammatory diseases including rheumatoid arthritis (RA). This review discusses the current understanding of NLRP3 activation in RA pathogenesis and its impact on innate and adaptive immunity, as well as the potential application of specific NLRP3 inhibitors as therapeutic strategies for RA.
NOD-like receptor family pyrin domain-containing 3 (NLRP3) inflammasome is a cytoplasmic multiprotein complex composed of the innate immune receptor protein NLRP3, the adapter protein apoptosis-associate speck-like protein containing a caspase recruitment domain (ASC), and the inflammatory protease cysteine-1. Pathogen-associated molecular patterns (PAMPs) or other endogenous danger-associated molecular patterns (DAMPs) activate the NLRP3 inflammasome. As part of the innate immune response, activated NLRP3 promotes GSDMD-dependent pyroptosis, and IL-1 beta and IL-18 are released during inflammation. Aberrantly activated NLRP3 is deeply involved in various inflammatory diseases. Due to its interaction with adaptive immunity. NLRP3 inflammation has increasingly received attention in autoimmune diseases. Rheumatoid arthritis (RA) is a classic autoimmune disease, which mainly causes bone and cartilage damage. Elevated levels of NLRP3 can be detected in the synovium of RA patients. NLRP3 overactivation is strongly associated with RA activity. Mouse models of spontaneous arthritis has shown that NLRP3/IL-1 beta axis is implicated in periarticular inflammation in RA. In this review, we describe the current understanding of NLRP3 activation in RA pathogenesis and dissect its impact on innate and adaptive immunity. We also discuss the potential application of specific inhibitors of NLRP3 to provide new therapeutic strategies for treating RA.

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