Interventional Radiology, Gustave Roussy, Villejuif, France
Laboratoire de Recherche Translationnelle en Immunothérapie (LRTI), INSERM U1015, Villejuif, France.
J Immunother Cancer. 2020 Jun;8(1). doi: 10.1136/jitc-2020-000579.
Intratumorous immunotherapy for cancer is currently thriving. The aim of such local strategy is to improve the therapeutic index of these treatments, for higher on-target/on-tumor activity and less on-target/off-tumor adverse events. Strategies allowing for slow release of anti-CTLA4 in the tumor microenvironment could improve their clinical efficacy.The purpose of the study was to develop a radiopaque delivery platform to improve the targeting and exposure of intratumorous anti-CTLA4 antibodies for cancer immunotherapy.
Pickering emulsions of anti-CTLA4 antibodies were formulated with radiopaque ethiodized oil and poly-lactic-co-glycolic acid (PLGA) nanoparticles. We characterized the microscopic aspect and stability of such emulsions using Turbiscan. We monitored the release of anti-CTLA4 over time from these emulsions and evaluated their structure using mass spectrometry. We then tested the functionality of the released antibodies by preforming ex vivo competitive binding assays. Finally, we assessed the in vivo efficacy of intratumorous anti-CTLA4 Pickering emulsions.
Pickering emulsions of ethiodized oil and PLGA nanoparticles (PEEPs) resulted in a radiopaque water-in-oil emulsion with average internal phase droplet size of 42±5 µm at day 7. Confocal microscopy showed that anti-CTLA4 antibodies were effectively encapsulated by ethiodized oil with PLGA nanoparticles located at the interface between the aqueous and the oily phase. Turbiscan analysis showed that emulsions were stable with continuous and progressive release of anti-CTLA4 antibodies reaching 70% at 3 weeks. Structural and functional analysis of the released antibodies did not show significant differences with native anti-CTLA4 antibodies. Finally, intratumorous anti-CTLA4 PEEPs were able to eradicate tumors and cure mice in a syngeneic immunocompetent preclinical tumor model.
Pickering emulsions of ethiodized oil and PLGA is an innovative radiopaque delivery platform that does not alter the functionality of anti-CTLA4 immune checkpoint antibodies. Beyond local anti-CTLA4 applications, these emulsions might be used with other therapeutic molecules for optimal intratumorous or intra-arterial delivery of novel cancer immunotherapies.
癌症的肿瘤内免疫疗法目前正在蓬勃发展。这种局部策略的目的是提高这些治疗方法的治疗指数,以提高针对肿瘤的/肿瘤内活性,减少针对肿瘤外的/肿瘤外不良事件。允许在肿瘤微环境中缓慢释放抗 CTLA4 的策略可以提高其临床疗效。本研究的目的是开发一种放射显影递药平台,以改善肿瘤内抗 CTLA4 抗体的靶向性和暴露度,用于癌症免疫治疗。
用放射显影的碘化油和聚乳酸-羟基乙酸共聚物(PLGA)纳米粒制备抗 CTLA4 抗体的 Pickering 乳液。我们使用 Turbiscan 来描述这种乳液的微观外观和稳定性。我们监测了这些乳液中抗 CTLA4 的释放情况,并使用质谱法评估了它们的结构。然后,我们通过进行体外竞争性结合测定来测试释放的抗体的功能。最后,我们评估了肿瘤内抗 CTLA4 Pickering 乳液的体内疗效。
碘化油和 PLGA 纳米粒的 Pickering 乳液(PEEPs)形成了一种放射显影的水包油乳液,第 7 天时内部相液滴的平均粒径为 42±5μm。共焦显微镜显示,抗 CTLA4 抗体被碘化油有效包裹,PLGA 纳米粒位于水相和油相之间的界面处。Turbiscan 分析表明,乳液具有稳定性,抗 CTLA4 抗体呈连续渐进释放,3 周时达到 70%。释放的抗体的结构和功能分析与天然抗 CTLA4 抗体没有显著差异。最后,肿瘤内抗 CTLA4 PEEPs 能够在同种异体免疫功能正常的临床前肿瘤模型中消除肿瘤并治愈小鼠。
碘化油和 PLGA 的 Pickering 乳液是一种创新的放射显影递药平台,不会改变抗 CTLA4 免疫检查点抗体的功能。除了局部抗 CTLA4 应用外,这些乳液还可与其他治疗分子一起用于优化新型癌症免疫疗法的肿瘤内或动脉内递药。