Manipulating T cell-mediated pathology: Targets and functions of monoclonal antibody immunotherapy

被引:11
作者
Martin, Aaron [1 ]
Tisch, Roland M. [1 ]
Getts, Daniel R. [2 ,3 ]
机构
[1] Univ N Carolina, Dept Microbiol & Immunol, Chapel Hill, NC 27515 USA
[2] Northwestern Univ, Feinberg Sch Med, Microbiol Immunol & Interdept Immunobiol Ctr, Chicago, IL 60625 USA
[3] Tolera Therapeut Inc, Dept Res & Dev, Kalamazoo, MI USA
关键词
Antibody dependent cellular cytotoxicity; Activation induced cell death; Anti-thymocyte globulin; Lymphocyte immune globulin; T cell receptor; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; IN-VIVO; MULTIPLE-SCLEROSIS; RECEPTOR REVISION; CHIMERIC ANTIBODIES; ALLOGRAFT-REJECTION; KIDNEY-TRANSPLANT; ANTIGEN RECEPTORS; SELF-TOLERANCE; BONE-MARROW;
D O I
10.1016/j.clim.2013.04.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Monoclonal antibody (mAb) technology has revolutionized treatment options for T cell mediated diseases. However, a safe, clinically available anti-T cell antibody (ab) remains elusive. Experience with anti-T cell agents and their propensity for causing immune-mediated toxicities have hampered the development of anti-T cell mAb's. Furthermore, misunderstanding regarding mechanism(s) of action of particular antibodies can influence development and clinical prescription habits. For example, the anti-CD3 Ab OKT3 is consistently described as a depleting Ab even though original studies showed the mechanism to be non-lytic. Future anti-T cell mAbs are likely to be non-depletional and focused on the expansion of regulatory T cells. This review discusses how the properties of Abs can be exploited for manipulating pathological T cell responses in the clinic. (C) 2013 The Authors. Published by Flsevier Inc. All rights reserved.
引用
收藏
页码:136 / 147
页数:12
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