基于纳米dlim2的联合治疗肺癌小鼠临床前研究

IF 1.1 Q3 BIOLOGY
Thi Hoa Le, Fan Sun, Gutian Xiao, Zhaoxia Qu
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引用次数: 0

摘要

本方案描述了一种基于纳米颗粒的治疗策略(nanoPDLIM2)的制备、给药和分析,该治疗策略与PD-1免疫检查点阻断免疫疗法和化疗相结合,用于小鼠肺癌的临床前研究。NanoPDLIM2使用基于聚乙烯亚胺(PEI)的递送系统,封装PDLIM2表达质粒,用于重建肿瘤中被抑制的PDLIM2。该方法可诱导肿瘤免疫原性,抑制耐药,与卡铂、紫杉醇、抗pd -1抗体联合使用,提高治疗效果。该方案描述了小鼠肺肿瘤诱导的步骤,纳米dlim2和其他治疗试剂的制备和给药,以及随后的肿瘤负荷、免疫反应和毒性分析,为研究人员提供了一个可重复的方法。•纳米dlim2的制备和交付的综合工作流程。•纳米dlim2联合PD-1阻断剂和化疗药物治疗肺癌疗效优越。•临床前肺癌模型中治疗试剂制备、给药、肿瘤检查、免疫分析、健康监测和毒性评估的详细协议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

NanoPDLIM2-Based Combination Therapy for Lung Cancer Treatment in Mouse Preclinical Studies.

NanoPDLIM2-Based Combination Therapy for Lung Cancer Treatment in Mouse Preclinical Studies.

NanoPDLIM2-Based Combination Therapy for Lung Cancer Treatment in Mouse Preclinical Studies.

NanoPDLIM2-Based Combination Therapy for Lung Cancer Treatment in Mouse Preclinical Studies.

This protocol describes the preparation, administration, and analysis of a nanoparticle-based therapeutic strategy (nanoPDLIM2) in combination with PD-1 immune checkpoint blockade immunotherapy and chemotherapy for the treatment of lung cancer in mouse preclinical studies. NanoPDLIM2 uses a polyethyleneimine (PEI)-based delivery system that encapsulates PDLIM2 expression plasmids for reconstituting PDLIM2 that is repressed in tumors. This approach induces tumor immunogenicity, suppresses drug resistance, and improves treatment efficacy when used in combination with carboplatin, paclitaxel, and anti-PD-1 antibodies. The protocol describes steps for mouse lung tumor induction, nanoPDLIM2 and other therapeutic reagents' preparation and administration, and subsequent analysis of tumor burden, immune response, and toxicity, providing a reproducible approach for investigators. Key features • Comprehensive workflow for preparation and delivery of nanoPDLIM2. • Combination of nanoPDLIM2 with PD-1 blockade and chemotherapeutics for superior efficacy in lung cancer treatment. • Detailed protocols for therapeutic reagents preparation, administration, tumor examination, immune analysis, health monitoring, and toxicity evaluation in a preclinical lung cancer model.

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CiteScore
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