扩大抗原特异性调节网络以治疗自身免疫
Xavier Clemente-Casares1, Jesus Blanco2,3, Poornima Ambalavanan1
1Julia McFarlane Diabetes Research Centre (JMDRC), and Department of Microbiology, Immunology and Infectious Diseases, Snyder Institute for Chronic Diseases and Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, Alberta T2N 4N1, Canada.
Nature
|February 18, 2016
概括
新的纳米粒子药物在体内扩展抗原特异性调节T细胞以治疗自身免疫性疾病. 这些疗法可以在不影响整体免疫力的情况下解决现有的自身免疫性疾病,从而提供一种特定疾病的治疗方法.
科学领域:
- 免疫学
- 纳米医学
- 自身免疫性疾病
背景情况:
- 调节性T细胞对于控制自身免疫性至关重要.
- 目前的方法缺乏抗原特异性调节T细胞的体内扩张.
- 开发针对自身免疫性疾病的向疗法是一个重大挑战.
研究的目的:
- 在体内研究-MHCII类纳米药物扩大抗原特异性调节T细胞的潜力.
- 评估这些纳米药物在解决已确定的自身免疫疾病方面的疗效.
- 探索pMHCII纳米药物调节免疫反应的机制.
主要方法:
- 用与pMHCII分子结合的自身免疫疾病相关被覆盖的纳米颗粒的系统输送.
- 使用各种小鼠模型,包括患者淋巴细胞的人性化模型.
- 评估了调控性CD4 ((+)) T细胞类型1 (TR1) 细胞的产生和扩张及其对自身免疫现象的影响.
主要成果:
- 在体内,pMHCII纳米药物成功触发了抗原特异性TR1类细胞的生成和扩张.
- 在不同小鼠模型中,已确定的自身免疫性疾病得到解决.
- 纳米药物诱导自反应性T细胞分化为TR1类细胞,抑制抗原呈现细胞,并促进调控性B细胞分化,而不会影响系统免疫力.
结论:
- 基于pMHCII的纳米药物代表了自身免疫性疾病的新疗法.
- 这些纳米药物为治疗广泛的自身免疫疾病提供了特定疾病的方法.
- 这些发现表明,对抗原特异性调节T细胞的体内扩张有希望.
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