Q1 · CROSS-FIELD
Article
Author: June, Carl H. ; Weissman, Drew ; Méndez Fernández, Pedro O. ; Yadegari, Amir ; Shewale, Swapnil V. ; Epstein, Jonathan A. ; Li, Li ; Papp, Tyler E. ; Aghajanian, Haig ; Tam, Ying K. ; Kimura, Toru ; Tombácz, István ; Parhiz, Hamideh ; Puré, Ellen ; Mui, Barbara L. ; Soliman, Ousamah Younoss ; Albelda, Steven M. ; Rurik, Joel G.
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