Abdominal aortic aneurysm (AAA) is a life-threatening condition characterized by the dilation of the abdominal aorta, leading to a high risk of rupture. Current treatment options are limited, particularly for patients ineligible for surgical interventions. This study explores a novel immunotherapeutic approach using chimeric antigen receptor Treg cells targeting vascular cell adhesion molecule-1 (VCAM-1) to mitigate AAA progression. By leveraging the specificity and regulatory function of CAR-Treg cells, our research aims to modulate the immune response and reduce inflammation in the aneurysmal wall. Results from preclinical mouse models demonstrated that CAR-Treg cells effectively homed to the aneurysmal site, suppressed local inflammation, and decreased aortic dilation compared to control groups. These findings suggest that CAR-Treg cell therapy could provide a promising, non-surgical treatment option for AAA patients, addressing a critical unmet need in cardiovascular disease management.
Targeting VCAM-1 with chimeric antigen receptor and regulatory T cell for abdominal aortic aneurysm treatment.
利用嵌合抗原受体和调节性T细胞靶向VCAM-1治疗腹主动脉瘤
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作者:Gang Qingwei, Lun Yu, Zhang Xiaoxu, Uzokov Jamol, Jiang Han, He Yuchen, Shen Shikai, Wang Shiyue, Erhart Philipp, Böckler Dittmar, Li Yuemeng, Han Yanshuo, Zhang Jian
| 期刊: | Communications Biology | 影响因子: | 5.100 |
| 时间: | 2025 | 起止号: | 2025 Aug 15; 8(1):1230 |
| doi: | 10.1038/s42003-025-08604-9 | 研究方向: | 细胞生物学 |
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