CD19
体内
离体
T细胞
转染
嵌合抗原受体
B细胞
化学
细胞生物学
体外
细胞
信使核糖核酸
细胞疗法
分子生物学
向性
归巢(生物学)
抗原
细胞培养
作者
Manav Jain,Savannah E. Est-Witte,Sydney R. Shannon,Sarah Y. Neshat,Xinjie Yu,Sydney A Dunham,Tina Tian,Leonardo Cheng,Jawaun J. Harris,Maximilian F. Konig,Stephany Y. Tzeng,Jonathan P. Schneck,J. Green
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-03-11
卷期号:12 (11): eadz1722-eadz1722
被引量:1
标识
DOI:10.1126/sciadv.adz1722
摘要
While chimeric antigen receptor (CAR) T cell therapies have demonstrated therapeutic efficacy against B cell malignancies, widespread implementation of these therapies is hindered by a cumbersome, ex vivo manufacturing process. Delivery of CAR-encoding messenger RNA (mRNA) to endogenous T cells can generate these therapeutic cells in vivo and streamline this manufacturing workflow. To accomplish this, T cell-activating ligands were conjugated to a biodegradable polymeric mRNA nanoparticle to form T cell-targeted particles. By conjugating multiple activating ligands, T cell transfection and stimulation in vitro was increased, and greater T cell transfection and selectivity in vivo was achieved compared to an untargeted particle. These nanoparticles can flexibly encapsulate mRNA cargos and were used to deliver anti-CD19 CAR mRNA in vivo, enabling depletion of 95% of B cells in the peripheral blood and 50% depletion of splenic B cells in healthy mice. These findings regarding nanoparticle tropism and their potential therapeutic efficacy highlight the importance of this nonviral, polymeric platform to address key limitations associated with current CAR T practices.
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