Chattopadhyay Saborni, Liao Yu-Pei, Wang Xiang, Nel André E
California NanoSystems Institute, University of California, Los Angeles, CA 90095, USA.
Division of NanoMedicine, Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA.
Bioengineering (Basel). 2023 Oct 16;10(10):1205. doi: 10.3390/bioengineering10101205.
Despite the formidable treatment challenges of pancreatic ductal adenocarcinoma (PDAC), considerable progress has been made in improving drug delivery via pioneering nanocarriers. These innovations are geared towards overcoming the obstacles presented by dysplastic stroma and fostering anti-PDAC immune reactions. We are currently conducting research aimed at enhancing chemotherapy to stimulate anti-tumor immunity by inducing immunogenic cell death (ICD). This is accomplished using lipid bilayer-coated nanocarriers, which enable the attainment of synergistic results. Noteworthy examples include liposomes and lipid-coated mesoporous silica nanoparticles known as "silicasomes". These nanocarriers facilitate remote chemotherapy loading, as well as the seamless integration of immunomodulators into the lipid bilayer. In this communication, we elucidate innovative ways for further improving chemo-immunotherapy. The first is the development of a liposome platform engineered by the remote loading of irinotecan while incorporating a pro-resolving lipoxin in the lipid bilayer. This carrier interfered in stromal collagen deposition, as well as boosting the irinotecan-induced ICD response. The second approach was to synthesize polymer nanoparticles for the delivery of mutated KRAS peptides in conjunction with a TLR7/8 agonist. The dual delivery vaccine particle boosted the generation of antigen-specific cytotoxic T-cells that are recruited to lymphoid structures at the cancer site, with a view to strengthening the endogenous vaccination response achieved by chemo-immunotherapy.
尽管胰腺导管腺癌(PDAC)的治疗面临巨大挑战,但通过开创性的纳米载体在改善药物递送方面已取得了相当大的进展。这些创新旨在克服发育异常的基质所带来的障碍,并促进抗PDAC免疫反应。我们目前正在进行旨在通过诱导免疫原性细胞死亡(ICD)来增强化疗以刺激抗肿瘤免疫的研究。这是通过使用脂质双层包裹的纳米载体来实现的,其能够取得协同效果。值得注意的例子包括脂质体和被称为“硅质体”的脂质包裹的介孔二氧化硅纳米颗粒。这些纳米载体有助于远程化疗药物加载,以及将免疫调节剂无缝整合到脂质双层中。在本通讯中,我们阐明了进一步改善化学免疫疗法的创新方法。第一种方法是开发一种脂质体平台,通过远程加载伊立替康进行工程设计,同时在脂质双层中掺入一种促消退脂氧素。这种载体干扰了基质胶原沉积,并增强了伊立替康诱导的ICD反应。第二种方法是合成聚合物纳米颗粒,用于递送突变的KRAS肽并结合TLR7/8激动剂。这种双重递送疫苗颗粒促进了抗原特异性细胞毒性T细胞的产生,这些细胞被募集到癌症部位的淋巴结构中,以加强化学免疫疗法所实现的内源性疫苗接种反应。