共递送纳米颗粒靶向 CAF，在实体瘤中同时激活 T 细胞和 NKT 细胞攻击

Aim to develop a fibroblast-activated protein-α (FAP-α) responsive nanoparticle delivery system, (α-GC/NAV)-CPC, which encapsulates navitoclax (NAV) and alpha-galactosylceramide (α-GC). Upon reaching tumor site, the nanoparticles would be disassembled by FAP-α in tumor. The released α-GC activates natural killer T (NKT) and in parallel, the released NAV eliminates cancer associated fibroblasts (CAFs), ultimately breaking down physical barrier and realizing potent anti-tumor activity.

To maintain the self-assembly ability and FAP-α responsiveness, the designed amphiphilic block polymers consist of PEG chain as the hydrophilic domain, terminal cholesterol as the hydrophobic domain and FAP-α degradable amino acid residue sequence linkage (Ala-Thr-Gly-Pro-Ala). At the tissue level, the tumor specific fibrosis barrier destroying ability of (α-GC/NAV)-CPC was investigated. Subsequently, the NAV and α-GC were co-encapsulated into nanoparticles. The tumor accumulation, tumoricidal and anti-metastasis efficacy were validated in triple negative breast cancer-bearing models.

This strategy can efficiently break down the cancer associated fibroblast based physical barrier. Encapsulated NAV can significantly decrease tumor interstitial fluid pressure (IFP), indicating as 4.9-fold lower than saline control group. Consequently, enhanced tumor infiltration and penetration of immune cells were observed. By quantitative flow-cytometry analysis, the abundances of NKT and T cells in tumors after (NAV/α-GC)-CPC treatment increased over 5 times and 4 times respectively, compared with saline treatment. Encouragingly, in in vivo models, (α-GC/NAV)-CPC treatment even led to 66.7% of mice achieving tumor eradication without recurrence. In further pulmonary metastasis challenge, mice treated with (α-GC/NAV)-CPC rarely displayed lung metastatic nodules.