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利用腺病毒进行癌症免疫治疗:激发细胞免疫并以细胞特异性方式进行靶向递送。

Harnessing adenovirus in cancer immunotherapy: evoking cellular immunity and targeting delivery in cell-specific manner.

作者信息

Zeng Miao, Zhang Wei, Li Yisheng, Yu Li

机构信息

Department of Hematology and Oncology, Shenzhen University General Hospital, International Cancer Center, Hematology Institution of Shenzhen University, Shenzhen University Medical School, Shenzhen University, Shenzhen, Guangdong, 518000, China.

Guangdong Key Laboratory for Biomedical Measurements and Ultrasound Imaging, School of Biomedical Engineering, Shenzhen University Health Science Center, Shenzhen, 518060, China.

出版信息

Biomark Res. 2024 Mar 25;12(1):36. doi: 10.1186/s40364-024-00581-1.

Abstract

Recombinant adenovirus (rAd) regimens, including replication-competent oncolytic adenovirus (OAV) and replication-deficient adenovirus, have been identified as potential cancer therapeutics. OAV presents advantages such as selective replication, oncolytic efficacy, and tumor microenvironment (TME) remodeling. In this perspective, the principles and advancements in developing OAV toolkits are reviewed. The burgeoning rAd may dictate efficacy of conventional cancer therapies as well as cancer immunotherapies, including cancer vaccines, synergy with adoptive cell therapy (ACT), and TME reshaping. Concurrently, we explored the potential of rAd hitchhiking to adoptive immune cells or stem cells, highlighting how this approach facilitates synergistic interactions between rAd and cellular therapeutics at tumor sites. Results from preclinical and clinical trials in which immune and stem cells were infected with rAd have been used to address significant oncological challenges, such as postsurgical residual tumor tissue and metastatic tissue. Briefly, rAd can eradicate tumors through various mechanisms, resulting from tumor immunogenicity, reprogramming of the TME, enhancement of cellular immunity, and effective tumor targeting. In this context, we argue that rAd holds immense potential for enhancing cellular immunity and synergistically improving antitumor effects in combination with novel cancer immunotherapies.

摘要

重组腺病毒(rAd)方案,包括具有复制能力的溶瘤腺病毒(OAV)和复制缺陷型腺病毒,已被确定为潜在的癌症治疗方法。OAV具有选择性复制、溶瘤功效和肿瘤微环境(TME)重塑等优势。从这个角度出发,本文综述了开发OAV工具包的原理和进展。新兴的rAd可能决定传统癌症疗法以及癌症免疫疗法的疗效,包括癌症疫苗、与过继性细胞疗法(ACT)的协同作用以及TME重塑。同时,我们探讨了rAd搭载过继性免疫细胞或干细胞的潜力,强调了这种方法如何促进rAd与肿瘤部位细胞疗法之间的协同相互作用。用rAd感染免疫细胞和干细胞的临床前和临床试验结果已被用于应对重大的肿瘤学挑战,如术后残留肿瘤组织和转移组织。简而言之,rAd可以通过多种机制根除肿瘤,这些机制源于肿瘤免疫原性、TME重编程、细胞免疫增强和有效的肿瘤靶向。在此背景下,我们认为rAd在增强细胞免疫以及与新型癌症免疫疗法联合协同提高抗肿瘤效果方面具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e98/10962185/4aea145c3e62/40364_2024_581_Fig1_HTML.jpg

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