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Potential Application of Tregitopes as Immunomodulating Agents in Multiple Sclerosis

机译:Tregitopes作为免疫调节剂在多发性硬化症中的潜在应用

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The induction of immunologic tolerance is an important clinical goal in autoimmunity. CD4+regulatory T (Treg) cells, defined by the expression of the transcription factor forkhead box P3 (FoxP3), play a central role in the control of autoimmune responses. Quantitative and qualitative defects of Tregs have been postulated to contribute to failed immune regulation in multiple sclerosis (MS) and other autoimmune diseases. This paper highlights the potential uses of T regulatory cell epitopes (Tregitopes), natural Treg epitopes found to be contained in human immunoglobulins, as immunomodulating agents in MS. Tregitopes expand Treg cells and induce “adaptive Tregs” resulting in immunosuppression and, therefore, are being considered as a potential therapy for autoimmune diseases. We will compare Tregitopes versus intravenous immunoglobulin (IVIg) in the treatment of EAE with emphasis on the potential applications of Tregitope for the treatment of MS.
机译:免疫耐受的诱导是自身免疫的重要临床目标。由转录因子叉头盒P3(FoxP3)的表达定义的CD4 +调节性T(Treg)细胞在自身免疫反应的控制中起着核心作用。据推测,Treg的数量和质量缺陷会导致多发性硬化症(MS)和其他自身免疫性疾病免疫调节失败。本文重点介绍了T调节细胞表位(Tregitopes)的潜在用途,T调节细胞表位是人类免疫球蛋白中包含的天然Treg表位,可作为MS中的免疫调节剂。 Tregitopes扩展Treg细胞并诱导“适应性Treg”,从而导致免疫抑制,因此被认为是自身免疫性疾病的潜在疗法。我们将比较Tregitope与静脉注射免疫球蛋白(IVIg)在EAE的治疗中,重点是Tregitope在MS治疗中的潜在应用。

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