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Biomimetic Liposome with Surface‐Bound Elastase for Enhanced Tumor Penetration and Chemo‐Immumotherapy

Yongjiang Li, Junyong Wu, Xiong-Bin Hu, Tianjinhao Ding, Tiantian Tang, Daxiong Xiang

2021Advanced Healthcare Materials46 citationsDOI

Abstract

Dense extracellular matrix (ECM) in the tumor stroma has been a challenge for drug penetration and cytotoxic T lymphocyte (CTL) infiltration. Neutrophil elastase (NE), in surface-bound form, can destruct ECM rapidly, may be used for remodeling tumor ECM, and overcoming tumor stromal barrier. Focusing on elastosis in triple-negative breast tumor, biomimetic liposomes with chimeric cell membrane proteins (LMP) are developed and for the first time, it is demonstrated that LMP with surface-bound elastase (NE-LMP) can target and degrade ECM effectively in tumor stroma, with minimal toxicity to normal tissues. The pretreatment of NE-LMP increases the accumulation of chemotherapeutics at the tumor site and enhances antitumor effects. Also, NE-LMP facilitates CTL infiltration in tumors and exhibits enhanced chemo-immunotherapy in combination of PD-1 immune checkpoint blockade treatment in orthotopic 4T1 tumor-bearing mice, with significantly prolonged survival. Moreover, the remodeling of the tumor ECM by NE-LMP shows inhibiting effects on metastasis in the lung. Findings from this study suggest that NE-LMP holds promise for enhancing deep penetration of drug and infiltration of CTL in desmoplastic tumor by effective degrading ECM in the tumor stroma.

Topics & Concepts

CTL*Stromal cellExtracellular matrixStromaCancer researchInfiltration (HVAC)ElastaseImmune systemCytotoxic T cellTumor microenvironmentChemistryMaterials scienceCell biologyImmunologyBiologyCD8ImmunohistochemistryIn vitroBiochemistryEnzymeComposite materialCancer Cells and MetastasisImmunotherapy and Immune ResponsesNanoplatforms for cancer theranostics
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