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:Chimeric antigen receptor therapy for hepatocellular carcinoma.
将 CAR-T 细胞疗法在血液系统恶性肿瘤中的成功经验应用于实体瘤,已成为当前研究活动的重点。
将CAR-T 细胞疗法在血液系统恶性肿瘤中的成功经验应用于实体瘤,已成为当前研究活动的主要焦点。然而,实体瘤带来的独特挑战,如免疫细胞浸润有限、T细胞持久性降低以及抗原丢失,导致早期临床试验仅取得有限成功。近年来,将下一代装甲CAR T细胞与多种替代免疫细胞类型相结合的联合策略,重新点燃了该领域的乐观情绪。肝细胞癌因其肝脏微环境的独特特征而成为一种独特的实体,这些特征包括脂质代谢、胆汁酸以及来自肠-肝轴的微生物化合物的影响。此外,HCC具有多种肿瘤特异性和肿瘤相关抗原,使得靶向方法能够在最小化脱靶毒性的风险下实施。HCC的独特复杂性,以及导致这些肿瘤的潜在肝脏疾病,为细胞疗法带来了挑战和机遇。在这篇综述中,我们考察了CAR T细胞疗法治疗HCC的当前格局,重点介绍了近期的临床和临床前进展。此外,我们讨论了为什么鉴于肝脏特定的解剖学和免疫学特性,HCC可能特别适合定制化的基于CAR的策略。
Adapting the success of chimeric antigen receptor T cell therapy from hematologic malignancies to solid tumors has become a major focus of ongoing research activities. However, the unique challenges posed by solid tumors, such as limited immune cell infiltration, reduced T cell persistence, and antigen loss, have led to only limited success in early clinical trials. Recently, combinatorial strategies incorporating next-generation armored CAR T cells along with various alternative immune cell types have rekindled optimism in the field. Hepatocellular carcinoma represents a distinct entity due to the unique characteristics of the liver microenvironment, including the influence of lipid metabolism, bile acids, and microbial compounds from the gut-liver axis. Furthermore, HCC is characterized by a variety of tumor-specific and tumor-associated antigens, enabling targeted approaches with minimal risk of on-target/off-tumor effects. The unique complexity of HCC, along with the underlying liver diseases that give rise to these tumors, presents both challenges and opportunities for cellular therapies. In this review, we examine the current landscape of CAR T cell therapy for HCC, highlighting recent clinical and preclinical developments. Furthermore, we discuss why HCC may be especially well-suited for tailored CAR-based strategies, given the liver's specific anatomical and immunological properties.
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