The role of C5a receptors in autoimmunity.


Journal

Immunobiology
ISSN: 1878-3279
Titre abrégé: Immunobiology
Pays: Netherlands
ID NLM: 8002742

Informations de publication

Date de publication:
09 2023
Historique:
received: 14 04 2023
revised: 04 06 2023
accepted: 10 06 2023
medline: 29 8 2023
pubmed: 21 8 2023
entrez: 20 8 2023
Statut: ppublish

Résumé

The complement system is an essential component of the innate immune response and plays a vital role in host defense and inflammation. Dysregulation of the complement system, particularly involving the anaphylatoxin C5a and its receptors (C5aR1 and C5aR2), has been linked to several autoimmune diseases, indicating the potential for targeted therapies. C5aR1 and C5aR2 are seven-transmembrane receptors with distinct signaling mechanisms that play both partially overlapping and opposing roles in immunity. Both receptors are expressed on a broad spectrum of immune and non-immune cells and are involved in cellular functions and physiological processes during homeostasis and inflammation. Dysregulated C5a-mediated inflammation contributes to autoimmune diseases such as rheumatoid arthritis, systemic lupus erythematosus, multiple sclerosis, epidermolysis bullosa acquisita, antiphospholipid syndrome, and others. Therefore, targeting C5a or its receptors may yield therapeutic innovations in these autoimmune diseases by reducing the recruitment and activation of immune cells that lead to tissue inflammation and injury, thereby exacerbating the autoimmune response. Clinical trials focused on the inhibition of C5 cleavage or the C5a/C5aR1-axis using small molecules or monoclonal antibodies hold promise for bringing novel treatments for autoimmune diseases into practice. However, given the heterogeneous nature of (systemic) autoimmune diseases, there are still several challenges, such as patient selection, optimal dosing, and treatment duration, that require further investigation and development to realize the full therapeutic potential of C5a receptor inhibition, ideally in the context of a personalized medicine approach. Here, we aim to provide a brief overview of the current knowledge on the function of C5a receptors, the involvement of C5a receptors in autoimmune disorders, the molecular mechanisms underlying C5a receptor-mediated autoimmunity, and the potential for targeted therapies to modulate their activity.

Identifiants

pubmed: 37598588
pii: S0171-2985(23)00081-5
doi: 10.1016/j.imbio.2023.152413
pii:
doi:

Substances chimiques

Receptor, Anaphylatoxin C5a 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

152413

Informations de copyright

Copyright © 2023 Elsevier GmbH. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Jovan Schanzenbacher (J)

Institute for Systemic Inflammation Research (ISEF), University of Lübeck, Lübeck, Germany.

Katja Hendrika Kähler (K)

Institute for Systemic Inflammation Research (ISEF), University of Lübeck, Lübeck, Germany.

Evelyn Mesler (E)

Institute for Systemic Inflammation Research (ISEF), University of Lübeck, Lübeck, Germany.

Marie Kleingarn (M)

Institute for Systemic Inflammation Research (ISEF), University of Lübeck, Lübeck, Germany.

Christian Marcel Karsten (C)

Institute for Systemic Inflammation Research (ISEF), University of Lübeck, Lübeck, Germany.

Daniel Leonard Seiler (D)

Institute for Systemic Inflammation Research (ISEF), University of Lübeck, Lübeck, Germany. Electronic address: daniel.seiler@uksh.de.

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Classifications MeSH