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引用次数: 0
摘要
胰腺导管腺癌(PDAC)是预后最差的消化道恶性肿瘤之一。CLDN18.2 CAR-T 疗法最近在 PDAC 中显示出良好的临床效果。放疗作为一种传统治疗方法,可诱导全身免疫激活和腹水效应。然而,二者联合治疗 PDAC 的协同效应和机制仍不甚明了。在这项研究中,我们开发了一种CLDN18.2特异性CAR-T,并将其应用于单侧和双侧小鼠肿瘤模型。结果表明,这种协同疗法不仅提高了单侧肿瘤小鼠的杀瘤效果,还诱导了双侧肿瘤模型中局部和远处肿瘤的消退。从机理上讲,早期辐射诱导的细胞凋亡促进了 CD8 + T 细胞的增殖,而局部和远处肿瘤部位趋化因子 CCL2 水平的升高促进了 CAR-T 和内源性 T 细胞的浸润,从而导致全身性肿瘤抑制。这项研究提出了将放疗与CAR-T疗法相结合治疗转移性胰腺癌的可行方法,阐明了CAR-T细胞增强放疗效果的体内机制,为抗击转移性胰腺癌提供了一种新策略。
Systemic tumor regression with synergy therapy: radiotherapy and CAR-T.
Pancreatic ductal adenocarcinoma (PDAC) is one of the most poorly prognostic digestive tract malignancies. CLDN18.2 CAR-T therapy has recently shown promising clinical effects in PDAC. Radiotherapy, a traditional treatment, can induce systemic immune activation and abscopal effects. However, the synergistic effect and mechanism of their combination in PDAC treatment remain poorly understood. In this study, we developed a CLDN18.2-specific CAR-T and applied it to unilateral and bilateral mouse tumor models. Our results demonstrated that this synergy therapy not only improved tumor-killing effects in unilateral tumor-bearing mice but also induced regression in both local and distant tumors in bilateral tumor models. Mechanistically, early radiation-induced apoptosis promoted the proliferation of CD8 + T cells, while increased chemokine CCL2 levels from localized and distant tumor sites facilitated CAR-T and endogenous T cell infiltration, leading to systemic tumor suppression. This study proposes a promising approach for treating metastatic pancreatic cancer by combining radiotherapy and CAR-T therapy, elucidating the mechanism of CAR-T cell-enhanced radiotherapy effects ex vivo, and highlighting a novel strategy for combating metastatic pancreatic cancer.
期刊介绍:
Cell Death Discovery is a multidisciplinary, international, online-only, open access journal, dedicated to publishing research at the intersection of medicine with biochemistry, pharmacology, immunology, cell biology and cell death, provided it is scientifically sound. The unrestricted access to research findings in Cell Death Discovery will foster a dynamic and highly productive dialogue between basic scientists and clinicians, as well as researchers in industry with a focus on cancer, neurobiology and inflammation research. As an official journal of the Cell Death Differentiation Association (ADMC), Cell Death Discovery will build upon the success of Cell Death & Differentiation and Cell Death & Disease in publishing important peer-reviewed original research, timely reviews and editorial commentary.
Cell Death Discovery is committed to increasing the reproducibility of research. To this end, in conjunction with its sister journals Cell Death & Differentiation and Cell Death & Disease, Cell Death Discovery provides a unique forum for scientists as well as clinicians and members of the pharmaceutical and biotechnical industry. It is committed to the rapid publication of high quality original papers that relate to these subjects, together with topical, usually solicited, reviews, editorial correspondence and occasional commentaries on controversial and scientifically informative issues.