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通过微波化疗免疫刺激 Ce-MnMOF 降低氧化还原水平逆转免疫抑制微环境,提高免疫治疗效果。

Reversing the immunosuppressive microenvironment with reduced redox level by microwave-chemo-immunostimulant Ce-Mn MOF for improved immunotherapy.

机构信息

Laboratory of Controllable Preparation and Application of Nanomaterials, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.

CAS Key Laboratory of Cryogenics, Technical Institute of Physics and Chemistry, Beijing, 100190, China.

出版信息

J Nanobiotechnology. 2022 Dec 3;20(1):512. doi: 10.1186/s12951-022-01699-w.

Abstract

BACKGROUNDS

Reversing the immunosuppressive tumor microenvironment (TME) in the tumor is widely deemed to be an effective strategy to improve immune therapy. In particular, the redox balance in TME needs to be well controlled due to its critical role in mediating the functions of various cells, including cancer cells and immune-suppressive cells.

RESULTS

Here, we propose an efficient strategy to reshape the redox homeostasis to reverse immunosuppressive TME. Specifically, we developed a microwave-chemo-immunostimulant CMMCP to promote the infiltration of the tumor-T cells by simultaneously reducing the reactive oxygen species (ROS) and glutathione (GSH) and improving the oxygen (O) levels in TME. The CMMCP was designed by loading chemotherapy drugs cisplatin into the bimetallic Ce-Mn MOF nanoparticles coated with polydopamine. The Ce-Mn MOF nanoparticles can effectively improve the catalytic decomposition of ROS into O under microwave irradiation, resulting in overcoming hypoxia and limited ROS generation. Besides, the activity of intracellular GSH in TME was reduced by the redox reaction with Ce-Mn MOF nanoparticles. The reprogrammed TME not only boosts the immunogenic cell death (ICD) induced by cisplatin and microwave hyperthermia but also gives rise to the polarization of pro-tumor M2-type macrophages to the anti-tumor M1-type ones.

CONCLUSION

Our in vivo experimental results demonstrate that the microwave-chemo-immunostimulant CMMCP significantly enhances the T cell infiltration and thus improves the antitumor effect. This study presents an easy, safe, and effective strategy for a whole-body antitumor effect after local treatment.

摘要

背景

逆转肿瘤中的免疫抑制肿瘤微环境(TME)被广泛认为是改善免疫治疗的有效策略。特别是,由于 TME 中的氧化还原平衡在介导包括癌细胞和免疫抑制细胞在内的各种细胞的功能方面起着关键作用,因此需要很好地控制其氧化还原平衡。

结果

在这里,我们提出了一种有效的策略来重塑氧化还原稳态,以逆转免疫抑制性 TME。具体而言,我们开发了一种微波化疗免疫刺激剂 CMMCP,通过同时降低活性氧(ROS)和谷胱甘肽(GSH)并改善 TME 中的氧(O)水平来促进肿瘤-T 细胞的浸润。CMMCP 是通过将化疗药物顺铂装载到包覆聚多巴胺的双金属 Ce-Mn MOF 纳米粒子中而设计的。Ce-Mn MOF 纳米粒子可以在微波照射下有效催化将 ROS 有效转化为 O,从而克服缺氧和有限的 ROS 生成。此外,TME 中的细胞内 GSH 的活性通过与 Ce-Mn MOF 纳米粒子的氧化还原反应而降低。重编程的 TME 不仅增强了顺铂和微波热疗诱导的免疫原性细胞死亡(ICD),而且导致促肿瘤 M2 型巨噬细胞向抗肿瘤 M1 型巨噬细胞的极化。

结论

我们的体内实验结果表明,微波化疗免疫刺激剂 CMMCP 显著增强了 T 细胞的浸润,从而提高了抗肿瘤效果。这项研究提出了一种简便、安全、有效的全身抗肿瘤效应策略,可用于局部治疗后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ebd/9719648/6e0217375cda/12951_2022_1699_Fig1_HTML.jpg

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