利用 CD8 靶向 mRNA-LNP 体内重编程 CD22 CAR-T 细胞以治疗血液系统恶性肿瘤
Reprogramming CD22 CAR-T cells in vivo using CD8-targeted mRNA-LNPs to treat hematological malignancies.
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FOR TREATMENT
现在就能报名的(招募中)排在最前,共 0 项。同一状态内中国中心优先。信息来自 ClinicalTrials.gov 与 CDE 公开登记。能否入组、费用与可及性,以登记原文和主治医生判断为准。
FOR RESEARCH
Reprogramming CD22 CAR-T cells in vivo using CD8-targeted mRNA-LNPs to treat hematological malignancies.
AI-guided CAR designs and targeted pathway modulation to enhance multi-antigen CAR T cell durability and overcome antigen escape.
IDR-induced CAR condensation improves the cytotoxicity of CAR-Ts against low-antigen cancers.
Unlocking T cell exhaustion: Insights and implications for CAR-T cell therapy.
CAR T-cell therapy landscape in pediatric, adolescent and young adult oncology - A comprehensive analysis of clinical trials.
Establishment and validation of in-house cryopreserved CAR/TCR-T cell flow cytometry quality control.
我们开发并验证了一种可行且可靠的方法,用于建立冷冻保存的 CAR/TCR T 细胞库,作为流式细胞术质量控制品,可作为 CAR/TCR T 细胞产品过程中和批次放行检测的质量控制标准。
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