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单次输注工程化长寿命多功能 T 细胞可使哮喘小鼠获得持久缓解。

A single infusion of engineered long-lived and multifunctional T cells confers durable remission of asthma in mice.

机构信息

State Key Laboratory of Molecular Oncology, Institute for Immunology, Beijing Key Laboratory for Immunological Research on Chronic Diseases, School of Basic Medical Sciences, Tsinghua University, Beijing, China.

SXMU-Tsinghua Collaborative Innovation Center for Frontier Medicine, Shanxi Medical University, Taiyuan, China.

出版信息

Nat Immunol. 2024 Jun;25(6):1059-1072. doi: 10.1038/s41590-024-01834-9. Epub 2024 May 27.

Abstract

Asthma, the most prevalent respiratory disease, affects more than 300 million people and causes more than 250,000 deaths annually. Type 2-high asthma is characterized by interleukin (IL)-5-driven eosinophilia, along with airway inflammation and remodeling caused by IL-4 and IL-13. Here we utilize IL-5 as the targeting domain and deplete BCOR and ZC3H12A to engineer long-lived chimeric antigen receptor (CAR) T cells that can eradicate eosinophils. We call these cells immortal-like and functional IL-5 CAR T cells (5T) cells. 5T cells were further modified to secrete an IL-4 mutein that blocks IL-4 and IL-13 signaling, designated as 5T4 cells. In asthma models, a single infusion of 5T4 cells in fully immunocompetent mice, without any conditioning regimen, led to sustained repression of lung inflammation and alleviation of asthmatic symptoms. These data show that asthma, a common chronic disease, can be pushed into long-term remission with a single dose of long-lived CAR T cells.

摘要

哮喘是最常见的呼吸道疾病,影响超过 3 亿人,每年导致超过 25 万人死亡。2 型高反应性哮喘的特点是白细胞介素(IL)-5 驱动的嗜酸性粒细胞增多,以及由 IL-4 和 IL-13 引起的气道炎症和重塑。在这里,我们利用 IL-5 作为靶向结构域,并消耗 BCOR 和 ZC3H12A 来设计能够消除嗜酸性粒细胞的长寿命嵌合抗原受体(CAR)T 细胞。我们称这些细胞为类永生和功能性 IL-5 CAR T 细胞(5T)细胞。5T 细胞进一步被修饰以分泌一种阻断 IL-4 和 IL-13 信号的 IL-4 突变体,命名为 5T4 细胞。在哮喘模型中,在完全免疫功能正常的小鼠中单次输注 5T4 细胞,无需任何预处理方案,可导致肺部炎症持续抑制和哮喘症状缓解。这些数据表明,哮喘是一种常见的慢性疾病,可以通过单次输注长寿命 CAR T 细胞来长期缓解。

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