靶向 PPP1R14B 通过 Nrf2/CX3CL1 轴恢复 CD8(+) T 细胞浸润,从而克服前列腺癌的免疫治疗耐药
Targeting PPP1R14B overcomes immunotherapy resistance in prostate cancer by restoring CD8(+) T-cell infiltration via the Nrf2/CX3CL1 axis.
肿瘤细胞治疗研究
DISEASE HUB
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、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
Targeting PPP1R14B overcomes immunotherapy resistance in prostate cancer by restoring CD8(+) T-cell infiltration via the Nrf2/CX3CL1 axis.
Piggybacking toward Progress for CAR T-Cell Therapy in Prostate Cancer.
Phase I Trial of P-PSMA-101 CAR T Cells in Patients with Metastatic Castration-Resistant Prostate Cancer.
P-PSMA-101 CAR-T 细胞的强劲扩增导致了毒性,但也在 mCRPC 患者中产生了持久缓解。未来 CAR-T 疗法的试验可能会从这种非病毒工程、TSCM 细胞富集策略的结果中获得启示。参见 Lee 等人第 3417 页的相关评论。
Innovations in Diagnosis Immunotherapy and Combination Therapy of Prostate Cancer: A Patent-driven Analysis.
用于 PC 的新型免疫治疗方法包括免疫检查点抑制剂(PD-1/PD-L1、CTLA-4 抑制剂)、疫苗和过继性细胞疗法(CAR-T 细胞)。同样,靶向治疗包括雄激素受体信号抑制剂、PARP 抑制剂、PI3K/AKT/mTOR 通路抑制剂、酪氨酸激酶抑制剂(TKIs)和 DNA 修复通路靶向药物等。结论:生物标志物的最新创新有助于 PC 的早期诊断。PC 晚期可通过单一免疫治疗、靶向治疗或两者联合治疗来延长患者生存期和希望。
Radioligand therapy in combination with CAR T cells overcomes the heterogeneous immunosuppressive prostate tumor microenvironment.
Lanmodulin-Engineered Outer Membrane Vesicles for Synergistic Targeted Radio-Immunotherapy.
Development and Evaluation of a Bispecific Single-Chain Antibody Targeting PSMA and CD3 to Enhance T-Cell-Mediated Lysis.
PSMA-directed CAR-T cell therapy for metastatic castration-resistant prostate cancer: a next-generation engineering perspective on stem cell-derived i
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