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维持淋巴引流寡核苷酸佐剂多聚体胶束释放的热敏水凝胶改善全身性癌症免疫治疗。

Thermosensitive Hydrogel Sustaining the Release of Lymph-Draining Oligonucleotide Adjuvant Polyplex Micelles Improves Systemic Cancer Immunotherapy.

作者信息

Lucas Samuel N, Archer Paul A, Yoon Tae Hee, Manspeaker Margaret P, Levitan Maya, Kim Jihoon, Thomas Susan N

机构信息

Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia 30332, United States.

Parker H. Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.

出版信息

ACS Nano. 2025 Jun 17;19(23):21775-21791. doi: 10.1021/acsnano.5c05517. Epub 2025 Jun 3.

Abstract

Immune checkpoint blockade (ICB) immunotherapies are a powerful tool in the clinical management of cancer, but response rates to ICB remain limited, and treatment-related toxicities can be significant. Therapeutic efficacy of ICB can be enhanced by delivering synergistic immunomodulators to tumor-draining lymph nodes (TdLNs). However, achieving sustained release of small molecule immunomodulators into the lymphatics and TdLNs remains challenging. To address this limitation, a sustained release system for delivering an oligonucleotide adjuvant to lymph nodes (LNs) was developed. CpG oligonucleotide was complexed with a redox-responsive cationic polymer and mixed with F127--Gelatin to generate a thermosensitive hydrogel that releases lymph-draining polyplex micelles . This CpG/BPEI-SS-/F127--Gelatin (CpG-HG) system enhanced the quantity and duration of CpG delivery to TdLNs following locoregional administration compared with free drug and enabled targeted, potent, and prolonged immunomodulation within TdLNs from a single administration. This augmented, localized immune response synergized with systemic ICB treatment, both markedly amplifying the systemic circulating CD8+ T cell response and improving antitumor therapeutic efficacy while enabling ICB dose reduction. These results highlight the potential for this drug delivery system as an adjunct to existing clinical ICB protocols to improve patient outcomes.

摘要

免疫检查点阻断(ICB)免疫疗法是癌症临床管理中的一种强大工具,但对ICB的反应率仍然有限,且治疗相关毒性可能很大。通过将协同免疫调节剂递送至肿瘤引流淋巴结(TdLN),可提高ICB的治疗效果。然而,实现小分子免疫调节剂在淋巴管和TdLN中的持续释放仍然具有挑战性。为解决这一局限性,开发了一种用于将寡核苷酸佐剂递送至淋巴结(LN)的持续释放系统。将CpG寡核苷酸与氧化还原响应性阳离子聚合物复合,并与F127-明胶混合,以生成一种释放淋巴引流多聚体胶束的热敏水凝胶。与游离药物相比,这种CpG/BPEI-SS-/F-127-明胶(CpG-HG)系统在局部给药后增加了CpG向TdLN的递送量和持续时间,并能通过单次给药在TdLN内实现靶向、强效和持久的免疫调节。这种增强的局部免疫反应与全身ICB治疗协同作用,既能显著增强全身循环CD8+T细胞反应,提高抗肿瘤治疗效果,又能降低ICB剂量。这些结果突出了这种药物递送系统作为现有临床ICB方案辅助手段以改善患者预后的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccea/12177939/bfde5c26d7cf/nn5c05517_0001.jpg

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