Guangdong Key Laboratory of Nanomedicine, CAS-HK Joint Lab for Biomaterials, Shenzhen Engineering Laboratory of Nanomedicine and Nanoformulations, Shenzhen Institutes of Advanced Technology (SIAT), Chinese Academy of Sciences, Shenzhen, 518055, China.
Guangdong Key Laboratory for Research and Development of Natural Drugs, Guangdong Medical University, Dongguan, 523808, China.
Small. 2021 Apr;17(14):e2007494. doi: 10.1002/smll.202007494. Epub 2021 Mar 12.
Chimeric antigen receptor T cell (CAR-T) therapy has shown remarkable clinical success in eradicating hematologic malignancies. However, hostile microenvironment in solid tumors severely prevents CAR-T cells migrating, infiltrating, and killing. Herein, a nanoengineered CAR-T strategy is reported for enhancing solid tumor therapy through bioorthogonal conjugation with a nano-photosensitizer (indocyanine green nanoparticles, INPs) as a microenvironment modulator. INPs engineered CAR-T biohybrids (CT-INPs) not only retain the original activities and functions of CAR-T cells, but it is further armed with fluorescent tracing and microenvironment remodeling abilities. Irradiated with laser, CT-INPs demonstrate that mild photothermal intervention destroys the extracellular matrix, expanded blood vessels, loosened compact tissue, and stimulated chemokine secretion without damping CAR-T cell activities. Those regulations induce an immune-favorable tumor microenvironment for recruitment and infiltration of CT-INPs. CT-INPs triggered photothermal effects collapse the physical and immunological barriers of solid tumor, and robustly boosted CAR-T immunotherapy. Therefore, CAR-T biohybrids provide reliable treatment strategy for solid tumor immunotherapy via microenvironment reconstruction.
嵌合抗原受体 T 细胞(CAR-T)疗法在消除血液恶性肿瘤方面显示出了显著的临床成功。然而,实体瘤中恶劣的微环境严重阻止了 CAR-T 细胞的迁移、浸润和杀伤。在此,报道了一种纳米工程 CAR-T 策略,通过与纳米光敏剂(吲哚菁绿纳米颗粒,INPs)进行生物正交共轭作为微环境调节剂来增强实体瘤治疗。工程化的 INPs 修饰的 CAR-T 生物杂合体(CT-INPs)不仅保留了 CAR-T 细胞的原始活性和功能,而且还具有荧光示踪和微环境重塑能力。激光照射后,CT-INPs 表现出温和的光热干预会破坏细胞外基质、扩张血管、疏松致密组织并刺激趋化因子分泌,而不会抑制 CAR-T 细胞的活性。这些调节作用诱导了免疫有利的肿瘤微环境,有利于 CT-INPs 的募集和浸润。CT-INPs 引发的光热效应破坏了实体瘤的物理和免疫屏障,有力地增强了 CAR-T 免疫疗法。因此,CAR-T 生物杂合体通过微环境重建为实体瘤免疫治疗提供了可靠的治疗策略。