Synergistic integration of mRNA-LNP with CAR-engineered immune cells: Pioneering progress in immunotherapy

被引:2
|
作者
Chen, Zhaozhao [1 ,2 ]
Shu, Jinhui [1 ,2 ]
Hu, Yu [1 ,2 ]
Mei, Heng [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Inst Hematol, Tongji Med Coll, 1277 Jiefang Ave, Wuhan 430022, Hubei, Peoples R China
[2] Hubei Clin Med Ctr Cell Therapy Neoplast Dis, Wuhan 430022, Peoples R China
基金
中国国家自然科学基金;
关键词
CHIMERIC ANTIGEN RECEPTOR; AUTOREACTIVE B-CELLS; T-CELLS; IN-VIVO; GENE DELIVERY; THERAPY; GENERATION; PSEUDOURIDINE; MULTICENTER; MECHANISMS;
D O I
10.1016/j.ymthe.2024.09.019
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Chimeric antigen receptor T cell (CAR-T) therapy has emerged as a revolutionary approach in the treatment of malignancies. Despite its remarkable successes, this field continues to grapple with challenges such as scalability, safety concerns, limited therapeutic effect, in vivo persistence, and the need for precise control over CAR expression. In the post-pandemic era of COVID-19 vaccine immunization, the application of messenger RNA (mRNA) encapsulated within lipid nanoparticles (LNPs) has recently garnered significant attention as a potential solution to address these challenges. This review delves into the dynamic landscape of mRNA-LNP technology and its potential implications for CAR-engineered immune cell-based immunotherapy.
引用
收藏
页码:3772 / 3792
页数:21
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