Suppr超能文献

一种靶向CD47的抗体-毒素偶联物,与细菌毒素李斯特菌溶素O相连,用于癌症免疫治疗。

An antibody-toxin conjugate targeting CD47 linked to the bacterial toxin listeriolysin O for cancer immunotherapy.

作者信息

Schrank Benjamin R, Wang Yifan, Wu Annette, Tran Nhat, Lee DaeYong, Edwards Jared, Huntoon Kristin, Dong Shiyan, Ha JongHoon, Ma Yifan, Grippin Adam J, Jeong Seong Dong, Antony Abin, Chang Mengyu, Kang Minjeong, Gallup Thomas D, Koong Albert C, Li Jing, Yun Kyuson, Kim Betty Y S, Jiang Wen

机构信息

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Department of Neurology, Houston Methodist Research Institute, Houston, TX, USA.

出版信息

Nat Cancer. 2025 Mar;6(3):511-527. doi: 10.1038/s43018-025-00919-0. Epub 2025 Feb 25.

Abstract

Antigen-presenting cells phagocytose tumor cells and subsequently cross-present tumor-derived antigens. However, these processes are impeded by phagocytosis checkpoints and inefficient cytosolic transport of antigenic peptides from phagolysosomes. Here, using a microbial-inspired strategy, we engineered an antibody-toxin conjugate (ATC) that targets the 'don't eat me' signal CD47 linked to the bacterial toxin listeriolysin O from the intracellular bacterium Listeria monocytogenes via a cleavable linker (CD47-LLO). CD47-LLO promotes cancer cell phagocytosis by macrophages followed by LLO release and activation to form pores on phagolysosomal membranes that enhance antigen cross-presentation of tumor-derived peptides and activate cytosolic immune sensors. CD47-LLO treatment in vivo significantly inhibited the growth of both localized and metastatic breast and melanoma tumors and improved animal survival as a monotherapy or in combination with checkpoint blockade. Together, these results demonstrate that designing ATCs to promote immune recognition of tumor cells represents a promising therapeutic strategy for treating multiple cancers.

摘要

抗原呈递细胞吞噬肿瘤细胞,随后交叉呈递肿瘤衍生抗原。然而,这些过程受到吞噬作用检查点以及抗原肽从吞噬溶酶体向胞质低效转运的阻碍。在此,我们采用一种受微生物启发的策略,设计了一种抗体 - 毒素偶联物(ATC),它通过可裂解连接子靶向与细胞内细菌单核细胞增生李斯特菌的细菌毒素溶素O相连的“别吃我”信号CD47(CD47 - LLO)。CD47 - LLO促进巨噬细胞对癌细胞的吞噬作用,随后释放并激活LLO,在吞噬溶酶体膜上形成孔道,增强肿瘤衍生肽的抗原交叉呈递并激活胞质免疫传感器。体内CD47 - LLO治疗显著抑制局部和转移性乳腺癌及黑色素瘤肿瘤的生长,并作为单一疗法或与检查点阻断联合使用时提高动物存活率。总之,这些结果表明,设计促进肿瘤细胞免疫识别的ATC代表了一种治疗多种癌症的有前景的治疗策略。

相似文献

5
Engineered CD47 protects T cells for enhanced antitumour immunity.工程化 CD47 保护 T 细胞以增强抗肿瘤免疫。
Nature. 2024 Jun;630(8016):457-465. doi: 10.1038/s41586-024-07443-8. Epub 2024 May 15.

本文引用的文献

5
Rise of Antibody-Drug Conjugates: The Present and Future.抗体药物偶联物的兴起:现状与未来。
Am Soc Clin Oncol Educ Book. 2023 May;43:e390094. doi: 10.1200/EDBK_390094.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验