嵌合抗原受体
生物
体内
基因组编辑
病毒载体
计算生物学
基因
CD19
遗传增强
离体
基因传递
核糖核酸
细胞生物学
基因组
DNA
转导(生物物理学)
分子生物学
RNA编辑
细胞
抄写(语言学)
癌症研究
基因表达
体外
转染
质粒
抗原
转录激活物样效应核酸酶
基因靶向
合成生物学
载体(分子生物学)
细胞因子释放综合征
作者
Cecilia Cotta‐Ramusino,Albert De Iaco,James B. Rottman,Jason Rodriguez,Donghui Li,Kartika Venugopal,Jessica Desmond,Christina Ferren,Mohit Gupta,Rebecca Levy,Rahul Palchaudhuri,Z. Jane Wang,William Querbes,Hari Pujar,Michael C. Holmes
出处
期刊:Blood
[Elsevier BV]
日期:2025-11-03
卷期号:146 (Supplement 1): 6097-6097
被引量:5
标识
DOI:10.1182/blood-2025-6097
摘要
Abstract Autologous ex vivo Chimeric Antigen Receptor (CAR) T-cell therapies are a powerful treatment option for relapsed and refractory leukemias and lymphomas. However, significant challenges limit access to these therapies, including long vein-to-vein times for drug delivery, viral vector supply chain constraints, and complex manufacturing processes. While allogeneic CAR-T therapies offer an alternative, they have not yet matched the therapeutic efficacy of conventional autologous T-cell therapies, highlighting the need for in vivo treatment solutions. RNA Gene Writers are designed to edit cellular genomes using RNA templates by harnessing the mechanism of target-primed reverse transcription (TPRT). These Gene Writers can be engineered to perform various editing reactions, from introducing gene-length DNA sequences to rewriting genomic regions by making single-nucleotide substitutions to small insertions or deletions. These edits can be achieved by delivering all-RNA compositions to primary cells in vitro or in vivo, eliminating the need for viral vectors and DNA template-based genome editing methods. For in vivo applications, targeting and editing of resting T cells remains a critical hurdle to overcome. Using T cell targeted LNPs (tLNPs), we co-delivered Gene Writer mRNA and a CD19 CAR template to human primary T cells in vitro, without pre-activation, and generated an average of ~40% CD19 CAR+ cells. These CAR+ T cells were observed to be functional, driving cytotoxicity, cytokine production, and cell expansion in response to multiple tumor types in vitro. For in vivo proof-of-concept studies, we tested two humanized xenograft mouse models for CAR specific activity. We performed a single intravenous infusion of tLNPs formulated with Gene Writer mRNA and a CD19 CAR template in a tumor-bearing xenograft mouse model. This generated an average of 24% CAR-T cells in vivo that subsequently expanded and eradicated tumor burden. Additionally, tLNP delivery of Gene Writer mRNA with a CD20 CAR template in a CD34+ engrafted humanized mouse model achieved an average of 55% CD20 CAR+ T-cells at peak expansion as well as complete elimination and sustained clearance of human B cells, highlighting its therapeutic potential in autoimmune diseases. Central to demonstrating the therapeutic potential of in vivo CAR-T in humans is the development of proof-of-concept studies in non-human primate (NHP) models. We tested our lead candidates in vitro and found that our Gene Writing system and tLNPs were cross reactive and generated up to 60% CAR writing in NHP T cells. To evaluate the delivery system in vivo in NHP, we used tLNPs formulated with a transient GFP mRNA reporter and observed approximately 40% of T cells expressed GFP, with minimal delivery to B cells. This enables a path towards in vivo NHP editing, either through Gene Writer-mediated permanent T cell editing or transient T cell engineering by CAR mRNA delivery. The ability to generate CAR-T cells in vivo using Gene Writers and our proprietary tLNP delivery platform provides a unique opportunity to potentially eliminate the challenges associated with conventional ex vivo CAR-T cell therapies and viral-based in vivo CAR-T gene therapies for both oncology and autoimmune diseases.
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