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产氧冷冻凝胶恢复缺氧肿瘤中T细胞介导的细胞毒性。

Oxygen-Generating Cryogels Restore T Cell Mediated Cytotoxicity in Hypoxic Tumors.

作者信息

Colombani Thibault, Eggermont Loek J, Hatfield Stephen M, Rogers Zachary J, Rezaeeyazdi Mahboobeh, Memic Adnan, Sitkovsky Michail V, Bencherif Sidi A

机构信息

Department of Chemical Engineering, Northeastern University, Boston, MA 02115, USA.

New England Inflammation and Tissue Protection Institute, Northeastern University, 360 Huntington Avenue, Boston, MA 02115, USA.

出版信息

Adv Funct Mater. 2021 Sep 9;31(37). doi: 10.1002/adfm.202102234. Epub 2021 Jun 23.

Abstract

Solid tumors are protected from antitumor immune responses due to their hypoxic microenvironments. Weakening hypoxia-driven immunosuppression by hyperoxic breathing of 60% oxygen has shown to be effective in unleashing antitumor immune cells against solid tumors. However, efficacy of systemic oxygenation is limited against solid tumors outside of lungs and has been associated with unwanted side effects. As a result, it is essential to develop targeted oxygenation alternatives to weaken tumor hypoxia as novel approaches to restore immune responses against cancer. Herein, we report on injectable oxygen-generating cryogels (O-cryogels) to reverse tumor-induced hypoxia. These macroporous biomaterials were designed to locally deliver oxygen, inhibit the expression of hypoxia-inducible genes in hypoxic melanoma cells, and reduce the accumulation of immunosuppressive extracellular adenosine. Our data show that O-cryogels enhance T cell-mediated secretion of cytotoxic proteins, restoring the killing ability of tumor-specific CTLs, both in vitro and in vivo. In summary, O-cryogels provide a unique and safe platform to supply oxygen as a co-adjuvant in hypoxic tumors and have the potential to improve cancer immunotherapies.

摘要

实体瘤因其缺氧的微环境而免受抗肿瘤免疫反应的影响。通过吸入60%的氧气进行高氧呼吸来减弱缺氧驱动的免疫抑制,已被证明对释放针对实体瘤的抗肿瘤免疫细胞有效。然而,全身氧合对肺部以外的实体瘤的疗效有限,并且与不良副作用有关。因此,开发有针对性的氧合替代方法以减弱肿瘤缺氧,作为恢复针对癌症的免疫反应的新方法至关重要。在此,我们报告了可注射的产氧冷冻凝胶(O-冷冻凝胶)以逆转肿瘤诱导的缺氧。这些大孔生物材料旨在局部输送氧气,抑制缺氧黑色素瘤细胞中缺氧诱导基因的表达,并减少免疫抑制性细胞外腺苷的积累。我们的数据表明,O-冷冻凝胶增强了T细胞介导的细胞毒性蛋白分泌,在体外和体内均恢复了肿瘤特异性CTL的杀伤能力。总之,O-冷冻凝胶提供了一个独特且安全的平台,可在缺氧肿瘤中作为辅助剂提供氧气,并有可能改善癌症免疫疗法。

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