In vivo site-specific engineering to reprogram T cells.
СтатьяПоддержка NIH: внешняя программаНазвание и аннотация: Перевод в очереди
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Nyberg William A, Bernard Pierre-Louis, Ngo Wayne, Wang Charlotte H, Ark Jonathan, Rothrock Allison, Borgo Gina M, Kimmerly Gabriella R, Jung Jae Hyung, Allain Vincent, Hamilton Jennifer R, Baldwin Alisha, Stickels Robert, Wyman Sarah, Khan Safwaan H, Lang Shanshan, Marsh Donna, Almudhfar Niran, Novick Catherine, Mortazavi Yasaman, Zhang Shimin, AbdElwakil Mahmoud M, Sandoval Luis R, Hwang Sidney, Chu Simon N, Jung Hyuncheol, Liu Chang, Sharma Devesh, McCreary Travis, Li Zhongmei, Satpathy Ansuman T, Carnevale Julia, Rutishauser Rachel L, Cromer M Kyle, Roybal Kole T, Dodgson Stacie E, Doudna Jennifer A, Asokan Aravind, Eyquem Justin
Аннотация
Engineered T cells, reprogrammed to express chimeric antigen receptors (CAR) or T cell receptors (TCR), have transformed cancer treatment and are being explored as therapeutics for autoimmune and infectious diseases. Enhancing T cell function through genome editing, either by disrupting endogenous genes or precisely inserting DNA payloads, has shown considerable promise1. However, the ex vivo manufacturing process is lengthy and costly, limiting accessibility of these therapies. In vivo generation of CAR T cells could overcome these barriers, but current methods rely either on transient expression with limited durability, or on random integration of DNA payloads that lack specificity. Here we demonstrate that stable and cell-specific transgene expression can be achieved through in vivo site-specific integration of large DNA payloads. We developed a two-vector system to deliver CRISPR-Cas9 ribonucleoproteins and a DNA donor template, using enveloped delivery vehicles and adeno-associated viruses, respectively. We optimized both vectors for T cell-specific delivery and gene-targeting efficiency. By integrating a CAR transgene into a T cell-specific locus, we generate therapeutic levels of CAR T cells in vivo in humanized mouse models of B cell aplasia, and haematological and solid malignancies. These findings offer a pathway to more efficient, precise and widely accessible T cell therapies.