Abstract
Inflammation drives pathology in many human diseases for which there are no disease-modifying drugs. Inflammasomes are signalling platforms that can induce pathological inflammation and tissue damage, having potential as an exciting new class of drug targets. Small-molecule inhibitors of the NLRP3 inflammasome that are now in clinical trials have demonstrated proof of concept that inflammasomes are druggable, and so drug development programmes are now focusing on other key inflammasome molecules. In this Review, we describe the potential of inflammasome components as candidate drug targets and the novel inflammasome inhibitors that are being developed. We discuss how the signalling biology of inflammasomes offers mechanistic insights for therapeutic targeting. We also discuss the major scientific and technical challenges associated with drugging these molecules during preclinical development and clinical trials.
| Original language | English |
|---|---|
| Journal | Nature Reviews Immunology |
| Early online date | 09 Sept 2024 |
| DOIs | |
| Publication status | Early online date - 09 Sept 2024 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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Author Correction: Inflammasome components as new therapeutic targets in inflammatory disease
Coll, R. C. & Schroder, K., 05 Dec 2024, (Early online date) In: Nature Reviews Immunology. 620Research output: Contribution to journal › Comment/debate › peer-review
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Publisher Correction: Inflammasome components as new therapeutic targets in inflammatory disease
Coll, R. C. & Schroder, K., 05 Dec 2024, (Early online date) In: Nature Reviews Immunology. 590Research output: Contribution to journal › Article › peer-review
2 Link opens in a new tab Citations (Scopus)
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