未来SLE生物治疗的机遇

MD David Wofsy (Professor of Medicine and Microbiology/Immunology), MD, PhD David I. Daikh (Assistant Professor of Medicine)
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引用次数: 4

摘要

单克隆抗体的发展和重组DNA技术的出现使得鉴定和选择性抑制不同的细胞亚群、表面分子和分泌产物成为可能,这些细胞亚群、表面分子和分泌产物有助于正常和病理免疫反应。这些进展有助于阐明促进自身免疫性疾病的机制。因此,现在有可能考虑治疗这些疾病的合理战略。其中一些策略旨在影响细胞表面相互作用,这些相互作用决定了潜在的自身反应性T细胞在抗原刺激后是否被激活或耐受。其他策略则是增强或抑制调节自身免疫的不同细胞因子。所有这些策略都在系统性红斑狼疮的动物模型中显示出希望,并且它们可能很快转化为有效的人类新疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
9 Opportunities for future biological therapy in SLE

The development of monoclonal antibodies and the emergence of recombinant DNA technology has made it possible to identify and selectively inhibit distinct cell subsets, surface molecules and secreted products that contribute to normal and pathological immune responses. These advances have helped to clarify the mechanisms that promote autoimmune diseases. As a result, it is now possible to contemplate rational strategies for the treatment of these diseases. Some of these strategies are designed to influence the cell surface interactions that determine whether potentially autoreactive T cells become activated or tolerant following antigen stimulation. Other strategies are designed to augment or inhibit distinct cytokines that regulate autoimmunity. All of these strategies have shown promise in animal models for systemic lupus erythematosus, and they may soon be translated into effective new therapies for people.

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