The CD11b-integrin (ITGAM) and systemic lupus erythematosus

Author:

Fagerholm SC12,MacPherson M1,James MJ13,Sevier-Guy C14,Lau CS5

Affiliation:

1. Medical Research Institute, Ninewells Hospital and Medical School

2. Institute of Biotechnology, University of Helsinki, Finland

3. College of Life Sciences, University of Dundee, UK

4. National Health Service Tayside, UK

5. Division of Rheumatology and Clinical Immunology, Department of Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong

Abstract

Variations at the ITGAM gene, which encodes for the CD11b chain of the Mac-1 (alphaMbeta2; CD11b/CD18; complement receptor-3) integrin, is one of the strongest genetic risk factors for systemic lupus erythematosus (SLE). More specifically, a genetic variant (rs1143679) which results in an arginine to histidine substitution at position 77 in the extracellular portion of the integrin is associated with disease. It has recently been shown that this amino acid substitution results in a dysfunctional integrin, which is deficient in mediating cell adhesion to integrin ligands, phagocytosis and in addition cannot restrict inflammatory cytokine production in macrophages. In this review, we discuss immunological functions of the Mac-1 integrin and how defects in the genetic variant of Mac-1 may relate to SLE development.

Publisher

SAGE Publications

Subject

Rheumatology

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