Therapeutic Potential of Targeting Complement C5a Receptors in Diabetic Kidney Disease.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
15 May 2023
Historique:
received: 04 04 2023
revised: 26 04 2023
accepted: 28 04 2023
medline: 29 5 2023
pubmed: 27 5 2023
entrez: 27 5 2023
Statut: epublish

Résumé

Diabetic kidney disease (DKD) affects 30-40% of patients with diabetes and is currently the leading cause of end-stage renal disease (ESRD). The activation of the complement cascade, a highly conserved element of the innate immune system, has been implicated in the pathogenesis of diabetes and its complications. The potent anaphylatoxin C5a is a critical effector of complement-mediated inflammation. Excessive activation of the C5a-signalling axis promotes a potent inflammatory environment and is associated with mitochondrial dysfunction, inflammasome activation, and the production of reactive oxygen species. Conventional renoprotective agents used in the treatment of diabetes do not target the complement system. Mounting preclinical evidence indicates that inhibition of the complement system may prove protective in DKD by reducing inflammation and fibrosis. Targeting the C5a-receptor signaling axis is of particular interest, as inhibition at this level attenuates inflammation while preserving the critical immunological defense functions of the complement system. In this review, the important role of the C5a/C5a-receptor axis in the pathogenesis of diabetes and kidney injuries will be discussed, and an overview of the status and mechanisms of action of current complement therapeutics in development will be provided.

Identifiants

pubmed: 37240105
pii: ijms24108758
doi: 10.3390/ijms24108758
pmc: PMC10218149
pii:
doi:

Substances chimiques

Complement C5a 80295-54-1
Complement System Proteins 9007-36-7
Receptor, Anaphylatoxin C5a 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Inez A Trambas (IA)

Department of Diabetes, Central Clinical School, Monash University, Melbourne, VIC 3004, Australia.

Melinda T Coughlan (MT)

Department of Diabetes, Central Clinical School, Monash University, Melbourne, VIC 3004, Australia.

Sih Min Tan (SM)

Department of Diabetes, Central Clinical School, Monash University, Melbourne, VIC 3004, Australia.

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