装载靶向组织蛋白酶 G 的双 HLA 限制性 TCR 的 T 细胞可有效根除 AML
T cells dressed up with a dual HLA-restricted TCR targeting cathepsin G drive effective AML eradication.
肿瘤细胞治疗研究
MODALITY HUB
FOR TREATMENT
现在就能报名的(招募中)排在最前,共 2 项。同一状态内中国中心优先。信息来自 ClinicalTrials.gov、CDE 与 ChiCTR 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
T cells dressed up with a dual HLA-restricted TCR targeting cathepsin G drive effective AML eradication.
Current status and challenges of TCR-T cell therapy for AML/MDS.
mRNA vaccines in cancer immunotherapy: current progress and perspectives in solid tumors and hematologic malignancies.
A T-cell receptor targeting RUNX1 frameshift mutations in acute myeloid leukemia.
Identification of specific T-cell response and T-cell receptor targeting shared neoantigen for acute myeloid leukemia.
First-in-Human Study of MDG1011, a TCR-T Therapy Directed Against HLA-A*02:01-Restricted PRAME Antigen for High-Risk Myeloid and Lymphoid Neoplasms.
入组 CD-TCR-001 I 期部分的患者,在所研究的少数患者中显示出 MDG1011 潜在临床和生物学活性的迹象。
Targeting of acute myeloid leukemia by five-gene engineered T cells expressing transgenic T-cell receptor specific to WT1, chimeric antigenic receptor
所提出的策略利用单个 piggyBac 转座子载体,通过插入 TCR、CAR、BiTE 构建体以及 tEGFR 基因自杀系统,实现了 T 细胞特异性针对急性髓系白血病的复杂重定向。
Protective effects for HLA-B*40:01 and C*03:04 in NPM1-mutated AML: result of a large HLA association study.
基于这些发现,进一步研究应确认新表位特异性 T 细胞的存在与功能,并表征特异性 T 细胞受体(TCR)。序列信息最终可能被用于免疫治疗策略,通过 TCR 工程化 T 细胞或双特异性 TCR T/NK 细胞衔接器治疗急性髓系白血病(AML)患者。
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