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1 型糖尿病的耐受-抗原特异性免疫治疗问题。

A Question of Tolerance-Antigen-Specific Immunotherapy for Type 1 Diabetes.

机构信息

The University of Queensland Diamantina Institute, The University of Queensland, Woolloongabba, QLD, 4102, Australia.

Mater Research Institute UQ, The University of Queensland, Woolloongabba, QLD, 4102, Australia.

出版信息

Curr Diab Rep. 2020 Nov 9;20(12):70. doi: 10.1007/s11892-020-01363-3.

Abstract

PURPOSE OF REVIEW

Antigen-specific immunotherapy (ASI) is a long sought-after goal for type 1 diabetes (T1D), with the potential of greater long-term safety than non-specific immunotherapy. We review the most recent advances in identification of target islet epitopes, delivery platforms and the ongoing challenges.

RECENT FINDINGS

It is now recognised that human proinsulin contains a hotspot of epitopes targeted in people with T1D. Beta-cell neoantigens are also under investigation as ASI target epitopes. Consideration of the predicted HLA-specificity of the target antigen for subject selection is now being incorporated into trial design. Cell-free ASI approaches delivering antigen with or without additional immunomodulatory agents can induce antigen-specific regulatory T cell responses, including in patients and many novel nanoparticle-based platforms are under development. ASI for T1D is rapidly advancing with a number of modalities currently being trialled in patients and many more under development in preclinical models.

摘要

目的综述

抗原特异性免疫疗法(ASI)是 1 型糖尿病(T1D)长期以来追求的目标,其长期安全性可能优于非特异性免疫疗法。我们综述了鉴定胰岛靶点、递送平台方面的最新进展以及当前面临的挑战。

最近的发现

目前已认识到,人胰岛素原包含 T1D 患者靶向的热点表位。β细胞新抗原也正在作为 ASI 的目标表位进行研究。目前,在临床试验设计中已将针对目标抗原的预测 HLA 特异性纳入考虑。无细胞 ASI 方法可递送抗原,同时或不添加额外的免疫调节剂,可诱导抗原特异性调节性 T 细胞反应,包括在患者中,许多新的基于纳米颗粒的平台正在开发中。T1D 的 ASI 正在迅速发展,许多方法目前正在患者中进行试验,更多的方法正在临床前模型中进行开发。

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