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双管齐下的攻击:pH 驱动的膜锚定近红外双模式纳米光敏剂激发免疫原性细胞焦亡并隔离免疫检查点以增强前列腺癌光免疫治疗。

Dual-Pronged Attack: pH-Driven Membrane-Anchored NIR Dual-Type Nano-Photosensitizer Excites Immunogenic Pyroptosis and Sequester Immune Checkpoint for Enhanced Prostate Cancer Photo-Immunotherapy.

机构信息

Department of Urology, The First Affiliated Hospital of Soochow University, Suzhou, 215006, China.

Department of Urology, Dushu Lake Hospital Affiliated to Soochow University, Medical Center of Soochow University, Suzhou Dushu Lake Hospital, Suzhou, 215000, China.

出版信息

Adv Sci (Weinh). 2023 Oct;10(28):e2302422. doi: 10.1002/advs.202302422. Epub 2023 Aug 6.

Abstract

Prostate cancer (PCa) is a frustrating immunogenic "cold" tumor and generally receives unsatisfied immunotherapy outcomes in the clinic. Pyroptosis is an excellent immunogenic cell death form that can effectively activate the antitumor immune response, promote cytotoxic T-lymphocyte infiltration, and convert tumors from "cold" to "hot." However, the in vivo application of pyroptosis drugs is seriously limited, and the upregulation of tumor PD-L1 caused by photo-immunotherapy further promotes immune escape. Herein, a new nano-photosensitizer (YBS-BMS NPs-RKC) with pH-response integrating immunogenic pyroptosis induction and immune checkpoint blockade is developed. The pH-responsive polymer equipped with the cell membrane anchoring peptide RKC is used as the carrier and further encapsulated with the near-infrared-activated semiconductor polymer photosensitizer YBS and a PD-1/PD-L1 complex small molecule inhibitor BMS-202. The pH-driven membrane-anchoring and pyroptosis activation of YBS-BMS NPs-RKC is clearly demonstrated. In vitro and in vivo studies have shown that this dual-pronged therapy stimulates a powerful antitumor immune response to suppress primary tumor progression and evokes long-term immune memory to inhibit tumor relapse and metastasis. This work provides an effective self-synergistic platform for PCa immunotherapy and a new idea for developing more biocompatible photo-controlled pyroptosis inducers.

摘要

前列腺癌(PCa)是一种令人沮丧的免疫原性“冷”肿瘤,临床上通常对免疫治疗的效果不满意。细胞焦亡是一种极好的免疫原性细胞死亡形式,可有效激活抗肿瘤免疫反应,促进细胞毒性 T 淋巴细胞浸润,并将肿瘤由“冷”变“热”。然而,细胞焦亡药物的体内应用受到严重限制,光免疫疗法引起的肿瘤 PD-L1 上调进一步促进了免疫逃逸。在此,开发了一种具有 pH 响应性的新型纳米光敏剂(YBS-BMS NPs-RKC),可诱导免疫原性细胞焦亡和免疫检查点阻断。具有细胞膜锚定肽 RKC 的 pH 响应性聚合物被用作载体,并进一步封装近红外激活半导体聚合物光敏剂 YBS 和 PD-1/PD-L1 复合物小分子抑制剂 BMS-202。明确证明了 YBS-BMS NPs-RKC 的 pH 驱动的膜锚定和细胞焦亡激活。体外和体内研究表明,这种双管齐下的治疗方法刺激了强大的抗肿瘤免疫反应,抑制了原发性肿瘤的进展,并引起了长期的免疫记忆,以抑制肿瘤的复发和转移。这项工作为前列腺癌免疫治疗提供了一个有效的自协同平台,并为开发更具生物相容性的光控细胞焦亡诱导剂提供了一个新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1b/10558672/15e4c9bae307/ADVS-10-2302422-g001.jpg

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