Department of Dermatology, Northwestern University, Chicago, IL, United States.
Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL, United States.
Front Immunol. 2020 Dec 1;11:581433. doi: 10.3389/fimmu.2020.581433. eCollection 2020.
Vitiligo is an autoimmune skin disease characterized by melanocyte destruction. Regulatory T cells (Tregs) are greatly reduced in vitiligo skin, and replenishing peripheral skin Tregs can provide protection against depigmentation. Ganglioside D3 (GD3) is overexpressed by perilesional epidermal cells, including melanocytes, which prompted us to generate GD3-reactive chimeric antigen receptor (CAR) Tregs to treat vitiligo. Mice received either untransduced Tregs or GD3-specific Tregs to test the hypothesis that antigen specificity contributes to reduced autoimmune reactivity and . CAR Tregs displayed increased IL-10 secretion in response to antigen, provided superior control of cytotoxicity towards melanocytes, and supported a significant delay in depigmentation compared to untransduced Tregs and vehicle control recipients in a TCR transgenic mouse model of spontaneous vitiligo. The latter findings were associated with a greater abundance of Tregs and melanocytes in treated mice versus both control groups. Our data support the concept that antigen-specific Tregs can be prepared, used, and stored for long-term control of progressive depigmentation.
白癜风是一种自身免疫性皮肤疾病,其特征是黑色素细胞破坏。白癜风皮肤中的调节性 T 细胞(Tregs)大大减少,而补充外周皮肤 Tregs 可以提供对抗脱色的保护。神经节苷脂 D3(GD3)在病变周围表皮细胞中过度表达,包括黑色素细胞,这促使我们生成 GD3 反应性嵌合抗原受体(CAR)Tregs 来治疗白癜风。小鼠接受未转导的 Tregs 或 GD3 特异性 Tregs,以测试抗原特异性有助于减少自身免疫反应的假设,结果表明,CAR Tregs 对黑色素细胞的细胞毒性具有更好的控制作用,并在 TCR 转基因自发性白癜风小鼠模型中与未转导的 Tregs 和载体对照组相比,显著延迟了脱色。后者的发现与治疗小鼠中 Tregs 和黑色素细胞的丰度明显高于两组对照组有关。我们的数据支持这样一种概念,即可以制备、使用和储存抗原特异性 Tregs,以长期控制进行性脱色。