通过靶向肿瘤相关巨噬细胞的嵌合受体工程化溶瘤病毒重振内源性抗肿瘤免疫
Rejuvenating endogenous antitumor immunity via a chimeric receptor-engineered oncolytic virus targeting tumor-associated macrophages.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Patient-derived xenografts or organoids in the discovery of traditional and self-assembled drug for tumor immunotherapy.
Patient-derived xenografts or organoids in the discovery of traditional and self-assembled drug for tumor immunotherapy.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
除了免疫检查点抑制剂的快速发展外,自组装免疫治疗药物的开发也出现了激增。基于免疫靶点,传统肿瘤免疫治疗药物分为五类,即免疫检查点抑制剂、直接免疫调节剂、过继细胞疗法、溶瘤病毒和癌症疫苗。此外,具有更高精确性和环境敏感性的自组装药物的出现,为肿瘤免疫治疗提供了一种有前景的创新方法。尽管肿瘤免疫治疗药物开发进展迅速,但所有候选药物都需要进行临床前安全性和有效性评估,而传统评估主要使用二维细胞系和动物模型进行,这种方法可能不适用于免疫治疗药物。然而,患者来源的异种移植和类器官模型保持了病理性肿瘤异质性的异质性和免疫性。
In addition to the rapid development of immune checkpoint inhibitors, there has also been a surge in the development of self-assembly immunotherapy drugs. Based on the immune target, traditional tumor immunotherapy drugs are classified into five categories, namely immune checkpoint inhibitors, direct immune modulators, adoptive cell therapy, oncolytic viruses, and cancer vaccines.
Additionally, the emergence of self-assembled drugs with improved precision and environmental sensitivity offers a promising innovation approach to tumor immunotherapy.
Despite rapid advances in tumor immunotherapy drug development, all candidate drugs require preclinical evaluation for safety and efficacy, and conventional evaluations are primarily conducted using two-dimensional cell lines and animal models, an approach that may be unsuitable for immunotherapy drugs. The patient-derived xenograft and organoids models, however, maintain the heterogeneity and immunity of the pathological tumor heterogeneity.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。