Signaling lymphocyte activation molecule family in systemic lupus erythematosus.


Journal

Clinical immunology (Orlando, Fla.)
ISSN: 1521-7035
Titre abrégé: Clin Immunol
Pays: United States
ID NLM: 100883537

Informations de publication

Date de publication:
07 2019
Historique:
received: 11 07 2018
revised: 04 11 2018
accepted: 05 11 2018
pubmed: 12 11 2018
medline: 31 3 2020
entrez: 12 11 2018
Statut: ppublish

Résumé

Systemic lupus erythematosus (SLE) is a multifactorial autoimmune disease characterized by a breakdown in immune tolerance leading to the development of auto-reactive lymphocytes and autoantibodies. Recent findings have provided new insight on the role of the signaling lymphocytic activation molecule family (SLAMF) receptors, a group of nine co-regulatory molecules involved in the activation of hematopoietic cells, and their downstream protein SLAM-associated protein (SAP), into the pathogenesis of SLE. This review summarizes the current knowledge on SLAMF in human SLE immunopathogenesis, and the importance of SLAMF molecules as new therapeutic targets.

Identifiants

pubmed: 30415085
pii: S1521-6616(18)30442-X
doi: 10.1016/j.clim.2018.11.001
pii:
doi:

Substances chimiques

Signaling Lymphocytic Activation Molecule Family 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

57-63

Subventions

Organisme : NIAID NIH HHS
ID : P01 AI065687
Pays : United States

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

Auteurs

Denis Comte (D)

Divisions of Immunology and Allergy, Lausanne University Hospital, Lausanne, Switzerland. Electronic address: denis.comte@chuv.ch.

Maria P Karampetsou (MP)

Division of Rheumatology, Evaggelismos General Hospital, Athens, Greece.

Morgane Humbel (M)

Divisions of Immunology and Allergy, Lausanne University Hospital, Lausanne, Switzerland.

George C Tsokos (GC)

Harvard Medical School, Boston, MA, USA.

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Classifications MeSH