Therapeutic T-cell manipulation in rheumatoid arthritis: past, present and future

被引:49
作者
Isaacs, J. D. [1 ,2 ]
机构
[1] Univ Newcastle, Inst Cellular Med, Musculoskeletal Res Grp, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
[2] Univ Newcastle, Inst Cellular Med, Wilson Home Immunotherapy Ctr, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
基金
英国医学研究理事会;
关键词
rheumatoid arthritis; T cell; therapeutic tolerance; anti-CD3; immune modulation; monoclonal antibody; immunotherapy; co-stimulation blockade; autoimmunity; regulatory T cell;
D O I
10.1093/rheumatology/ken163
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Accumulating evidence suggests that RA is a T-cell-mediated autoimmune disease. Early attempts at disease modulation using strategies such as CD4 mAbs were severely hampered by a lack of biomarkers of autoreactivity. Recently, however, co-stimulation blockade has emerged as an effective treatment for RA. Alongside a greatly improved mechanistic understanding of immune regulation, this has rekindled hopes for authentic and robust immune programming. The final pieces of the jigsaw are not yet in place for RA but, in other disciplines, emerging treatment paradigms such as non-mitogenic anti-CD3 mAbs, autoantigenic peptides and even cellular therapies are providing hope for a future in which immunopathology can be specifically and vigorously curtailed.
引用
收藏
页码:1461 / 1468
页数:8
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