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设计一种可注射的多肽水凝胶储库,内含免疫检查点抑制剂 Anti-PD-L1 和阿霉素,以增强抗肿瘤联合治疗。

Design of an Injectable Polypeptide Hydrogel Depot Containing the Immune Checkpoint Blocker Anti-PD-L1 and Doxorubicin to Enhance Antitumor Combination Therapy.

机构信息

Key Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, 130022, P. R. China.

University of Science and Technology of China, Hefei, 230026, P. R. China.

出版信息

Macromol Biosci. 2021 Jun;21(6):e2100049. doi: 10.1002/mabi.202100049. Epub 2021 Apr 19.


DOI:10.1002/mabi.202100049
PMID:33871152
Abstract

Combination therapy can be used to enhance the therapeutic response and decrease side effects during cancer treatment. In this study, a system is developed to locally deliver the immune checkpoint blockade antibody targeting programmed death-ligand 1 (anti-PD-L1 or aPD-L1) and doxorubicin (Dox), by an injectable, biocompatible polypeptide hydrogel as a drug depot. The localized and sustained release of Dox after the intratumoral injection of the co-loaded hydrogel induces immunogenic tumor cell death, thus promoting an antitumor immunological response. The tumor inhibitory effect is significantly enhanced by the simultaneous release of aPD-L1 at the tumor site thanks to its action on the inhibition of the PD-1/PD-L1 pathway and restoration of the tumor-killing effect of cytotoxic T cells. Treatment of the B16F10 melanoma model with the aPD-L1 and Dox co-loaded hydrogel leads to a remarkable inhibition of tumor progression and prolongation of animal survival.

摘要

联合治疗可用于增强癌症治疗过程中的治疗反应并降低副作用。在这项研究中,开发了一种系统,通过可注射的、生物相容性的多肽水凝胶作为药物库来局部递送针对程序性死亡配体 1(抗 PD-L1 或 aPD-L1)和多柔比星(Dox)的免疫检查点阻断抗体。肿瘤内注射共载药水凝胶后,Dox 的局部和持续释放诱导免疫原性肿瘤细胞死亡,从而促进抗肿瘤免疫反应。由于 aPD-L1 在肿瘤部位的作用是抑制 PD-1/PD-L1 通路并恢复细胞毒性 T 细胞的杀伤作用,因此同时释放 aPD-L1 可显著增强肿瘤抑制作用。用载有 aPD-L1 和 Dox 的水凝胶治疗 B16F10 黑色素瘤模型可显著抑制肿瘤进展并延长动物存活时间。

相似文献

[1]
Design of an Injectable Polypeptide Hydrogel Depot Containing the Immune Checkpoint Blocker Anti-PD-L1 and Doxorubicin to Enhance Antitumor Combination Therapy.

Macromol Biosci. 2021-6

[2]
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[3]
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J Immunother Cancer. 2021-5

[4]
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[5]
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Nat Commun. 2021-4-23

[6]
Dual activity of PD-L1 targeted Doxorubicin immunoliposomes promoted an enhanced efficacy of the antitumor immune response in melanoma murine model.

J Nanobiotechnology. 2021-4-13

[7]
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[8]
Injectable Polypeptide Hydrogel Depots Containing Dual Immune Checkpoint Inhibitors and Doxorubicin for Improved Tumor Immunotherapy and Post-Surgical Tumor Treatment.

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[9]
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J Immunother Cancer. 2020-5

[10]
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引用本文的文献

[1]
Hydrogels as advanced drug delivery platforms for cancer immunotherapy: promising innovations and future outlook.

J Nanobiotechnology. 2025-7-28

[2]
Immune checkpoint blocking in cancer therapy using thermosensitive hydrogels: a review.

Naunyn Schmiedebergs Arch Pharmacol. 2025-5-2

[3]
Chiral polypeptide hydrogels regulating local immune microenvironment and anti-tumor immune response.

Nat Commun. 2025-1-31

[4]
Nanofibrous Peptide Hydrogels Leveraging Histidine to Modulate pH-Responsive Supramolecular Assembly and Antibody Release.

Biomacromolecules. 2025-1-13

[5]
Hydrogel systems for spatiotemporal controlled delivery of immunomodulators: engineering the tumor immune microenvironment for enhanced cancer immunotherapy.

Front Cell Dev Biol. 2024-12-13

[6]
Three-Dimensional Printing of Hydrogel Blend Tissue Engineering Scaffolds with In Situ Delivery of Anticancer Drug for Treating Melanoma Resection-Induced Tissue Defects.

J Funct Biomater. 2024-12-18

[7]
Hydrogel-based platforms for site-specific doxorubicin release in cancer therapy.

J Transl Med. 2024-9-30

[8]
Alternative Strategies for Delivering Immunotherapeutics Targeting the PD-1/PD-L1 Immune Checkpoint in Cancer.

Pharmaceutics. 2024-9-7

[9]
Polypeptide-Based Systems: From Synthesis to Application in Drug Delivery.

Pharmaceutics. 2023-11-20

[10]
Hydrogel drug delivery systems for minimally invasive local immunotherapy of cancer.

Adv Drug Deliv Rev. 2023-11

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