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针对多发性硬化症中致病 T 细胞的新型治疗策略。

Novel therapeutic strategies targeting the pathogenic T-cells in multiple sclerosis.

机构信息

University of Texas Southwestern Medical Center at Dallas, Department of Neurology, University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Boulevard, Dallas, TX 75390-9036, USA.

出版信息

Expert Rev Clin Immunol. 2005 Sep;1(3):345-55. doi: 10.1586/1744666X.1.3.345.

Abstract

Multiple sclerosis is a chronic disease in which immune cells incite inflammation in the central nervous system, ultimately resulting in the destruction of the myelin nerve sheath. Pathogenic CD4+ T-cells are believed to be responsible for initiating this process. Recent advances in molecular biology, such as transgenic and knockout animal models, genomics and proteomics, have allowed for a much greater understanding of the cellular and subcellular pathways involved in autoimmunity. The end result is an ever more specific array of potential therapeutic agents, each designed to target one component of the dysregulated immune system and in some cases, specific to each individual patient. The mechanisms, promises and pitfalls of these various strategies for the treatment of multiple sclerosis are the topic of this review.

摘要

多发性硬化症是一种慢性疾病,其中免疫细胞在中枢神经系统中引发炎症,最终导致髓鞘神经鞘的破坏。致病性 CD4+T 细胞被认为是引发这一过程的罪魁祸首。分子生物学的最新进展,如转基因和基因敲除动物模型、基因组学和蛋白质组学,使人们对自身免疫涉及的细胞和亚细胞途径有了更深入的了解。最终的结果是一系列越来越具体的潜在治疗药物,每种药物都旨在针对失调免疫系统的一个组成部分,在某些情况下,针对每个个体患者。本文综述了这些治疗多发性硬化症的各种策略的机制、前景和陷阱。

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