嵌合抗原受体
电穿孔
转染
基因传递
背景(考古学)
遗传增强
纳米技术
计算机科学
计算生物学
化学
医学
细胞培养
免疫疗法
生物
免疫学
材料科学
基因
免疫系统
古生物学
生物化学
遗传学
作者
Inês S. Pinto,Rosemeyre A. Cordeiro,Henrique Faneca
标识
DOI:10.1016/j.jconrel.2022.11.038
摘要
Chimeric antigen receptor T cell (CAR T cell) therapy is a revolutionary approach approved by the FDA and EMA to treat B cell malignancies and multiple myeloma. The production of these T cells has been done through viral vectors, which come with safety concerns, high cost and production challenges, and more recently also through electroporation, which can be extremely cytotoxic. In this context, nanosystems can constitute an alternative to overcome the challenges associated with current methods, resulting in a safe and cost-effective platform. However, the barriers associated with T cells transfection show that the design and engineering of novel approaches in this field are highly imperative. Here, we present an overview from CAR constitution to transfection technologies used in T cells, highlighting the lipid- and polymer-based nanoparticles as a potential delivery platform. Specifically, we provide examples, strengths and weaknesses of nanosystem formulations, and advances in nanoparticle design to improve transfection of T cells. This review will guide the researchers in the design and development of novel nanosystems for next-generation CAR T therapeutics.
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