Autoantibody IgG Protects Bone Erosion and Destruction in SLE Arthritis |Biomedgrid
Journal: American Journal of Biomedical Science & Research (Vol.11, No. 2)Publication Date: 2020-12-04
Authors : Guo Min Deng;
Page : 136-137
Keywords : Erythematosus; Monocytes; Arthritis; Osteoclast genesis; Autoimmune;
Abstract
Systemic lupus erythematosus (SLE) is a chronic autoimmune disease characterized by high levels of autoantibodies and multiorgan tissue damage [1]. Arthritis is common in patients with SLE [2]. Bone erosion is a remarkable feature in arthritis such as rheumatoid arthritis (RA), but they are usually absent in arthritis of SLE [3]. Thus, this is particularly striking for clinical doctors because synovial biopsies from SLE patients show similar synovial inflammation to those in RA [4]. Tissue deposited lupus IgG displays a key role in initiating inflammation in organ tissue including kidney, brain, skin and liver [5-7].
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