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

机译:T细胞介导的病理学操作:单克隆抗体免疫疗法的目标和功能

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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.
机译:单克隆抗体(mAb)技术彻底改变了T细胞介导疾病的治疗选择。但是,安全,临床上可用的抗T细胞抗体(ab)仍然难以捉摸。抗T细胞药物的经验及其引起免疫介导毒性的倾向已阻碍了抗T细胞单克隆抗体的开发。此外,对特定抗体作用机制的误解会影响发育和临床处方习惯。例如,抗CD3 Ab OKT3始终被描述为消耗抗体,即使原始研究表明该机制是非溶解性的。未来的抗T细胞单克隆抗体可能是非消耗性的,并且专注于调节性T细胞的扩增。这篇综述讨论了如何在临床中利用Abs的特性来操纵病理性T细胞反应。

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