决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Targeted immunotherapies for anaplastic lymphoma kinase-positive pediatric tumors: current advances and future perspectives.
Targeted immunotherapies for anaplastic lymphoma kinase-positive pediatric tumors: current advances and future perspectives.
儿童癌症的下一代治疗:通过联合疗法推进免疫治疗。
儿童癌症的下一代治疗:通过联合治疗推进免疫治疗。癌症仍然是儿童和青少年疾病相关死亡的主要原因之一。尽管治疗取得了进展,但许多儿童肿瘤的结局仍然有限,尤其是高危、复发或难治性疾病的患者。标准治疗,包括手术、化疗、放疗和干细胞移植,常常伴随严重的长期毒性和第二恶性肿瘤。耐药和复发仍然是主要的临床挑战。近年来癌症免疫治疗的进展彻底改变了成人肿瘤学,并且在几种儿童癌症中观察到了显著的临床进展。然而,在大多数实体瘤中,可比的获益仍然有限。在分子靶点中,间变性淋巴瘤激酶(ALK)已成为几种儿童恶性肿瘤中肿瘤发生的关键驱动因素,包括间变性大细胞淋巴瘤(ALCL)、神经母细胞瘤和炎性肌纤维母细胞瘤。虽然 ALK 酪氨酸激酶抑制剂已显示出临床获益,但耐药的出现凸显了对替代或补充策略的需求。ALK 可以作为肿瘤抗原,正如 ALK 阳性 ALCL 患者中自发的 ALK 特异性体液和 T 细胞反应所示,并且针对 ALK 的免疫治疗已被开发出来,并在 ALK 阳性肿瘤(包括 ALCL 和神经母细胞瘤)的临床前模型中显示出疗效。因此,针对 ALK 的免疫治疗代表了生物学上合理且有前景的方法,如果在临床试验中被证明安全有效,可能解决耐药问题并改善长期疾病控制。在这篇综述中,我们将讨论ALK特异性免疫疗法,包括ALK疫苗、ALK CAR-T和其他细胞疗法,以及靶向ALK的抗体,特别关注儿童ALK阳性肿瘤。
Next-Generation Treatment for Pediatric Cancer: Advancing Immunotherapy through Combinations. Cancer remains one of the leading causes of disease-related mortality among children and adolescents. Despite advances in treatments, outcomes for many pediatric tumors remain limited, particularly in patients with high-risk, relapsed, or refractory disease. Standard therapies, including surgery, chemotherapy, radiotherapy, and stem cell transplantation, are frequently associated with severe long-term toxicities and secondary malignancies. Resistance and relapse remain major clinical challenges. Recent progress in cancer immunotherapy has revolutionized adult oncology, and remarkable clinical advances have been observed in several pediatric cancers. However, comparable benefits in most solid tumors remain limited. Among molecular targets, anaplastic lymphoma kinase (ALK) has emerged as a critical driver of tumorigenesis in several pediatric malignancies, including anaplastic large cell lymphoma (ALCL), neuroblastoma and inflammatory myofibroblastic tumor. While ALK tyrosine kinase inhibitors have demonstrated clinical benefit, the emergence of resistance highlights the need for alternative or complementary strategies. ALK can act as an oncoantigen, as shown by spontaneous ALK-specific humoral and T-cell responses in patients with ALK-positive ALCL, and ALK-directed immunotherapies have been developed and have shown efficacy in preclinical models of ALK-positive tumors, including ALCL and neuroblastoma. Therefore, ALK-directed immunotherapies represent biologically rational and promising approaches that may, if proven safe and effective in clinical trials, address resistance and improve long-term disease control. In this review, we will discuss ALK-specific immunotherapies, including ALK vaccines, ALK CAR-T and other cellular therapies, as well as ALK-targeting antibodies with a particular focus on pediatric ALK-positive tumors.
MEMBER ACCOUNT
登录成功会直接打开下一页。