Costimulatory molecule CD154 in systemic lupus erythematosus and rheumatoid arthritis. Therapeutic perspectives
- PMID: 17877113
Costimulatory molecule CD154 in systemic lupus erythematosus and rheumatoid arthritis. Therapeutic perspectives
Abstract
SLE is a systemic autoimmune disease characterized by B cell hyperactivity. Evidence from the last years has shown that B cells play a key role in the development of the immune response. The interaction of CD40 on B cells with its ligand CD154 on activated T cells provides a costimulatory signal that induces T dependent B cell proliferation and differentiation with subsequent antibody production. Moreover, CD154 can act as a cytokine, in addition to its main role to mediate the interactions between T and CD40+ target cells. This review focuses on the multiple roles of CD154 in systemic lupus erythematosus and rheumatoid arthritis and its involvement in the humoral immunity disregulation of patients with these diseases. It also takes in consideration the most recent therapeutic perspectives regarding the use of monoclonal antibodies against CD154, which might be a powerful tool in the treatment of these diseases in the future.
Similar articles
-
Peripheral blood lymphocytes in SLE--hyperexpression of CD154 on T and B lymphocytes and increased number of double negative T cells.J Autoimmun. 1998 Oct;11(5):471-5. doi: 10.1006/jaut.1998.0213. J Autoimmun. 1998. PMID: 9802931
-
Mechanisms of CD23 hyperexpression on B cells from patients with rheumatoid arthritis.J Rheumatol. 2001 Jun;28(6):1222-8. J Rheumatol. 2001. PMID: 11409113
-
CD154-CD40 interactions mediate differentiation to plasma cells in healthy individuals and persons with systemic lupus erythematosus.Arthritis Rheum. 2002 Jun;46(6):1417-29. doi: 10.1002/art.10287. Arthritis Rheum. 2002. PMID: 12115170 Review. No abstract available.
-
The role of CD40-CD154 interactions in autoimmunity and the benefit of disrupting this pathway.Autoimmunity. 2004 Sep-Nov;37(6-7):457-64. doi: 10.1080/08916930400002386. Autoimmunity. 2004. PMID: 15621572 Review.
-
IL-10 production in B cells is confined to CD154+ cells in patients with systemic lupus erythematosus.J Autoimmun. 2004 Dec;23(4):379-83. doi: 10.1016/j.jaut.2004.10.001. J Autoimmun. 2004. PMID: 15571932
Cited by
-
The signaling role of CD40 ligand in platelet biology and in platelet component transfusion.Int J Mol Sci. 2014 Dec 3;15(12):22342-64. doi: 10.3390/ijms151222342. Int J Mol Sci. 2014. PMID: 25479079 Free PMC article. Review.
-
Aberrant CD40-induced NF-κB activation in human lupus B lymphocytes.PLoS One. 2012;7(8):e41644. doi: 10.1371/journal.pone.0041644. Epub 2012 Aug 27. PLoS One. 2012. PMID: 22952582 Free PMC article.
-
The role of microRNA-1246 in the regulation of B cell activation and the pathogenesis of systemic lupus erythematosus.Clin Epigenetics. 2015 Mar 14;7(1):24. doi: 10.1186/s13148-015-0063-7. eCollection 2015. Clin Epigenetics. 2015. PMID: 25789080 Free PMC article.
-
Neutralization of CD40 ligand costimulation promotes bone formation and accretion of vertebral bone mass in mice.Rheumatology (Oxford). 2018 Jun 1;57(6):1105-1114. doi: 10.1093/rheumatology/kex525. Rheumatology (Oxford). 2018. PMID: 29522194 Free PMC article.
-
Orbital fibroblasts from patients with thyroid-associated ophthalmopathy overexpress CD40: CD154 hyperinduces IL-6, IL-8, and MCP-1.Invest Ophthalmol Vis Sci. 2009 May;50(5):2262-8. doi: 10.1167/iovs.08-2328. Epub 2008 Dec 30. Invest Ophthalmol Vis Sci. 2009. PMID: 19117935 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical
Research Materials