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Inflammasome components as new therapeutic targets in inflammatory disease.
Coll, Rebecca C; Schroder, Kate.
Afiliación
  • Coll RC; Wellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK. R.Coll@qub.ac.uk.
  • Schroder K; Institute for Molecular Bioscience (IMB), The University of Queensland, St Lucia, Queensland, Australia. K.Schroder@imb.uq.edu.au.
Nat Rev Immunol ; 2024 Sep 09.
Article en En | MEDLINE | ID: mdl-39251813
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.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Nat Rev Immunol Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Nat Rev Immunol Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido
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