Claudin-18.2:从分子机制到实体瘤临床转化(综述)
Claudin-18.2: Molecular mechanisms to clinical translation in solid tumors (Review).
肿瘤细胞治疗研究
FRONTIER PAPERS
近 5 年肿瘤细胞治疗领域的研究论文。默认按评分排序(权威性 + 新鲜度)。
Claudin-18.2: Molecular mechanisms to clinical translation in solid tumors (Review).
Advances, challenges, and innovative strategies of CAR-T cell therapy in pancreatic cancer.
Preclinical Development and a Case Report of a Nanobody-Based CLDN18.2 CAR-T IMC002 with Reduced On-Target Off-Tumor Toxicity.
Systemic Therapy for Advanced Pancreatic Cancer in 2025: Current Standard-of-Care and Emerging Therapeutic Strategies.
Emerging Chimeric Antigen Receptor-Immune Cell Therapy for Pancreatic Cancer: Mechanisms, Clinical Advances, and Future Perspectives.
FNDC4 Drives Metastasis and Immune Evasion in Pancreatic Cancer.
VHH-based CAR-T cells targeting Claudin 18.2 show high efficacy in pancreatic cancer models.
本研究建立了一套开发 CLDN18.2 特异性 VHH 的有效框架,并证明其可成功整合到 CAR-T 细胞治疗中。
Local radiotherapy polarized tumor-associated macrophages enhance the efficacy of Claudin18.2-targeted CAR-T therapy in pancreatic cancer.
局部放疗显著增强了靶向 CLDN18.2 的 CAR-T 疗法对胰腺导管腺癌(PDAC)的抗肿瘤疗效。
IDO1 inhibition enhances CLDN18.2-CAR-T cell therapy in gastrointestinal cancers by overcoming kynurenine-mediated metabolic suppression in the tumor
靶向 IDO1 是克服胃肠道癌症免疫抑制屏障、提高 CLDN18.2-CAR-T 疗法疗效的一种有前景的策略。这些发现凸显了将 IDO1 抑制整合到 CAR-T 治疗方案中以解决难治性癌症耐药问题的潜力。
The high efficacy of claudin18.2-targeted CAR-T cell therapy in advanced pancreatic cancer with an antibody-dependent safety strategy.
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