A single infusion of engineered long-lived and multifunctional T cells confers durable remission of asthma in mice.
Gang JinYanyan LiuLixia WangZihao HeXiaocui ZhaoYuying MaYuting JiaZhuoyang LiNa YinMin PengPublished in: Nature immunology (2024)
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 IF ) cells. 5T IF cells were further modified to secrete an IL-4 mutein that blocks IL-4 and IL-13 signaling, designated as 5T IF 4 cells. In asthma models, a single infusion of 5T IF 4 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.
Keyphrases
- induced apoptosis
- cell cycle arrest
- chronic obstructive pulmonary disease
- lung function
- oxidative stress
- endoplasmic reticulum stress
- type diabetes
- signaling pathway
- low dose
- allergic rhinitis
- cystic fibrosis
- depressive symptoms
- electronic health record
- metabolic syndrome
- machine learning
- rheumatoid arthritis
- cancer therapy
- skeletal muscle