CAR T cells produced in vivo to treat cardiac injury
医学
体内
细胞生物学
离体
药理学
炎症
作者
Joel G. Rurik,István Tombácz,Amir Yadegari,Pedro O Méndez Fernández,Swapnil V. Shewale,Li Li,Toru Kimura,Ousamah Younoss Soliman,Tyler E. Papp,Ying K. Tam,Barbara L. Mui,Steven M. Albelda,Ellen Puré,Carl H. June,Haig Aghajanian,Drew Weissman,Hamideh Parhiz,Jonathan A. Epstein,Joel G. Rurik,István Tombácz
出处
期刊:Science [American Association for the Advancement of Science (AAAS)] 日期:2022-01-06卷期号:375 (6576): 91-96被引量:993
Making CAR T cells in vivo Cardiac fibrosis is the stiffening and scarring of heart tissue and can be fatal. Rurik et al . designed an immunotherapy strategy to generate transient chimeric antigen receptor (CAR) T cells that can recognize the fibrotic cells in the heart (see the Perspective by Gao and Chen). By injecting CD5-targeted lipid nanoparticles containing the messenger RNA (mRNA) instructions needed to reprogram T lymphocytes, the researchers were able to generate therapeutic CAR T cells entirely inside the body. Analysis of a mouse model of heart disease revealed that the approach was successful in reducing fibrosis and restoring cardiac function. The ability to produce CAR T cells in vivo using modified mRNA may have a number of therapeutic applications. —PNK