CD81 通过阻断 CD274/PD-L1 的选择性自噬降解驱动放射抵抗性胶质母细胞瘤的免疫逃逸
CD81 drives immune evasion in radioresistant glioblastoma by blocking selective autophagic degradation of CD274/PD-L1.
我们的工作确立了CD81作为连接放射抵抗与免疫逃逸的关键桥梁,其通过维持GBM中CD274的丰度发挥作用,并突显CD81作为优化放射免疫治疗的有前景的治疗靶点。
英文原题:Counteracting Immunosuppression in the Tumor Microenvironment by Oncolytic Newcastle Disease Virus and Cellular Immunotherapy.
癌症患者中存在自发性系统性T细胞介导的抗肿瘤免疫反应的证据,尤其是在其骨髓中观察到的,与外周局部肿瘤生长之间存在着明显的悖论。
癌症患者中存在自发性系统性T细胞介导的抗肿瘤免疫反应的证据,尤其是在其骨髓中观察到的证据,与外周局部肿瘤生长之间存在着明显的悖论。这种现象被称为“伴随免疫”,提示局部肿瘤及其肿瘤微环境(TME)阻止了系统性抗肿瘤免疫发挥有效作用。溶瘤新城疫病毒(NDV)具有固有的抗肿瘤和免疫刺激特性,能够打破治疗耐药性和免疫抑制。本综述更新了关于TME免疫抑制的最新信息,并讨论了溶瘤病毒,特别是NDV,以及细胞免疫治疗如何抵消TME免疫抑制效应的机制。关于细胞免疫治疗,本综述介绍了在免疫健全小鼠中进行的术后主动特异性免疫治疗和过继性T细胞介导治疗的临床前研究。在肿瘤攻击的T细胞缺陷nu/nu小鼠中进行记忆T细胞(MTC)转移,证明了这些细胞的持久性和功能性。小鼠中的移植物抗白血病(GvL)研究证明了晚期疾病包括转移和恶病质的完全缓解。在人肿瘤异种移植NOD/SCID小鼠中使用人类细胞进行的T细胞免疫治疗研究证明,骨髓来源的MTC优于血液来源的MTC。所介绍的临床研究结果包括使用两种不同类型的NDV修饰癌症疫苗的疫苗接种研究,以及一项使用再激活的骨髓来源癌症反应性MTC的初步过继性T细胞介导治疗研究。作为针对具有免疫抑制性TME的肿瘤进行临床免疫治疗可预期效果的一个例子,本文呈现了来自侵袭性脑肿瘤多形性胶质母细胞瘤的疫苗接种研究结果。过去几十年在病毒学、肿瘤学和免疫学领域的基础研究可被视为一段成功的历史。基于这些研究领域的发现,转化研究和临床研究通过引入并纳入免疫治疗,改变了癌症的治疗方式。
An apparent paradox exists between the evidence for spontaneous systemic T cell- mediated anti-tumor immune responses in cancer patients, observed particularly in their bone marrow, and local tumor growth in the periphery. This phenomenon, known as "concomitant immunity" suggests that the local tumor and its tumor microenvironment (TME) prevent systemic antitumor immunity to become effective. Oncolytic Newcastle disease virus (NDV), an agent with inherent anti-neoplastic and immune stimulatory properties, is capable of breaking therapy resistance and immunosuppression. This review updates latest information about immunosuppression by the TME and discusses mechanisms of how oncolytic viruses, in particular NDV, and cellular immunotherapy can counteract the immunosuppressive effect of the TME. With regard to cellular immunotherapy, the review presents pre-clinical studies of post-operative active-specific immunotherapy and of adoptive T cell-mediated therapy in immunocompetent mice. Memory T cell (MTC) transfer in tumor challenged T cell-deficient nu/nu mice demonstrates longevity and functionality of these cells. Graft-versus-leukemia (GvL) studies in mice demonstrate complete remission of late-stage disease including metastases and cachexia. T cell based immunotherapy studies with human cells in human tumor xenotransplanted NOD/SCID mice demonstrate superiority of bone marrow-derived as compared to blood-derived MTCs. Results from clinical studies presented include vaccination studies using two different types of NDV-modified cancer vaccine and a pilot adoptive T-cell mediated therapy study using re-activated bone marrow-derived cancer-reactive MTCs. As an example for what can be expected from clinical immunotherapy against tumors with an immunosuppressive TME, results from vaccination studies are presented from the aggressive brain tumor glioblastoma multiforme. The last decades of basic research in virology, oncology and immunology can be considered as a success story. Based on discoveries of these research areas, translational research and clinical studies have changed the way of treatment of cancer by introducing and including immunotherapy.
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