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抗自身免疫性脑脊髓炎的非炎性mRNA疫苗研制
作者:小柯机器人 发布时间:2021/1/8 16:38:37

德国约翰内斯·古腾堡大学医学院医学中心Ugur Sahin研究团队取得最新进展。他们研制了一种用于治疗实验性自身免疫性脑脊髓炎的非炎性mRNA疫苗。2021年1月8日出版的《科学》杂志发表了这项成果。
 
他们显示了系统地递送的纳米粒子配方的1甲基伪氨吡啶修饰的信使RNA(m1Ψ mRNA)编码与疾病相关的自身抗原,导致在没有共刺激信号的情况下在脾CD11c +抗原呈递细胞上呈递抗原。在多发性硬化的几种小鼠模型中,通过用这种m1Ψ mRNA治疗可以抑制疾病。治疗效果与效应T细胞的减少和调节性T细胞(Treg细胞)群体发育有关。明显地,这些Treg细胞执行强烈旁观免疫抑制,因此改善了由同源和非同源自身抗原诱导的疾病。
 
研究人员表示,控制自身反应性T细胞而不诱导全身性免疫抑制的能力是治疗自身免疫性疾病的主要目标。关键的挑战是在非炎性环境中安全有效地递送药学上明确定义的抗原。
 
附:英文原文

Title: A noninflammatory mRNA vaccine for treatment of experimental autoimmune encephalomyelitis

Author: Christina Krienke, Laura Kolb, Elif Diken, Michael Streuber, Sarah Kirchhoff, Thomas Bukur, zlem Akilli-ztürk, Lena M. Kranz, Hendrik Berger, Jutta Petschenka, Mustafa Diken, Sebastian Kreiter, Nir Yogev, Ari Waisman, Katalin Karikó, zlem Türeci, Ugur Sahin

Issue&Volume: 2021/01/08

Abstract: The ability to control autoreactive T cells without inducing systemic immune suppression is the major goal for treatment of autoimmune diseases. The key challenge is the safe and efficient delivery of pharmaceutically well-defined antigens in a noninflammatory context. Here, we show that systemic delivery of nanoparticle-formulated 1 methylpseudouridine-modified messenger RNA (m1Ψ mRNA) coding for disease-related autoantigens results in antigen presentation on splenic CD11c+ antigen-presenting cells in the absence of costimulatory signals. In several mouse models of multiple sclerosis, the disease is suppressed by treatment with such m1Ψ mRNA. The treatment effect is associated with a reduction of effector T cells and the development of regulatory T cell (Treg cell) populations. Notably, these Treg cells execute strong bystander immunosuppression and thus improve disease induced by cognate and noncognate autoantigens.

DOI: 10.1126/science.aay3638

Source: https://science.sciencemag.org/content/371/6525/145

期刊信息
Science:《科学》,创刊于1880年。隶属于美国科学促进会,最新IF:41.037