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免疫性疾病和器官移植中调节性 T 细胞输注治疗:优势与局限性的综述。

Therapy with regulatory T-cell infusion in autoimmune diseases and organ transplantation: A review of the strengths and limitations.

机构信息

University of Perugia, Department of Medicine and Surgery, Section of Pharmacology, Perugia, Italy.

Islamic Azad University, Department of Biochemistry, Kazerun, Iran.

出版信息

Transpl Immunol. 2024 Aug;85:102069. doi: 10.1016/j.trim.2024.102069. Epub 2024 Jun 4.

Abstract

In the last decade, cell therapies have revolutionized the treatment of some diseases, earning the definition of being the "third pillar" of therapeutics. In particular, the infusion of regulatory T cells (Tregs) is explored for the prevention and control of autoimmune reactions and acute/chronic allograft rejection. Such an approach represents a promising new treatment for autoimmune diseases to recover an immunotolerance against autoantigens, and to prevent an immune response to alloantigens. The efficacy of the in vitro expanded polyclonal and antigen-specific Treg infusion in the treatment of a large number of autoimmune diseases has been extensively demonstrated in mouse models. Similarly, experimental work documented the efficacy of Treg infusions to prevent acute and chronic allograft rejections. The Treg therapy has shown encouraging results in the control of type 1 diabetes (T1D) as well as Crohn's disease, systemic lupus erythematosus, autoimmune hepatitis and delaying graft rejection in clinical trials. However, the best method for Treg expansion and the advantages and pitfalls with the different types of Tregs are not fully understood in terms of how these therapeutic treatments can be applied in the clinical setting. This review provides an up-to-date overview of Treg infusion-based treatments in autoimmune diseases and allograft transplantation, the current technical challenges, and the highlights and disadvantages of this therapeutic approaches."

摘要

在过去的十年中,细胞疗法已经彻底改变了一些疾病的治疗方法,被誉为治疗的“第三支柱”。特别是,调节性 T 细胞(Tregs)的输注被用于预防和控制自身免疫反应和急性/慢性移植物排斥反应。这种方法代表了一种治疗自身免疫疾病的新的有前途的治疗方法,以恢复对自身抗原的免疫耐受,并防止对同种抗原的免疫反应。在体外扩增的多克隆和抗原特异性 Treg 输注治疗大量自身免疫性疾病的疗效在小鼠模型中得到了广泛证实。同样,实验工作也证明了 Treg 输注预防急性和慢性移植物排斥反应的疗效。Treg 治疗在控制 1 型糖尿病(T1D)以及克罗恩病、系统性红斑狼疮、自身免疫性肝炎和延迟移植物排斥方面显示出令人鼓舞的结果,临床试验。然而,在临床环境中应用这些治疗方法时,Treg 扩增的最佳方法以及不同类型 Treg 的优势和缺陷尚不完全清楚。本文综述了基于 Treg 输注的自身免疫性疾病和同种异体移植治疗的最新进展、当前的技术挑战以及这些治疗方法的亮点和不足。

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