Department of Pharmacy, Union Hospital, Tongji Medical College, HuaZhong University of Science and Technology, Wuhan, China; Tongji School of Pharmacy, HuaZhong University of Science and Technology, Wuhan, China; National Engineering Research Center for Nanomedicine, HuaZhong University of Science and Technology, Wuhan, China; Hubei Engineering Research Center for Novel Drug Delivery System, HuaZhong University of Science and Technology, Wuhan, China.
Tongji School of Pharmacy, HuaZhong University of Science and Technology, Wuhan, China; National Engineering Research Center for Nanomedicine, HuaZhong University of Science and Technology, Wuhan, China; Hubei Engineering Research Center for Novel Drug Delivery System, HuaZhong University of Science and Technology, Wuhan, China.
Nanomedicine. 2019 Jun;18:66-77. doi: 10.1016/j.nano.2019.02.008. Epub 2019 Mar 2.
Taking advantages of drug delivery system, immunostimulatory and chemotherapeutic agents with different physiochemical properties can be co-delivered to realize synergistic antitumor effect. Here the immunostimulatory cytokine interleukin-2 (IL-2) was firstly adsorbed in doxorubicin (DOX) loaded nanovesicles (NV-DOX) with high encapsulation efficiency by a facile solvent free method. After intravenous injection to melanoma bearing mice, NV-DOX can accumulate in tumor and remarkably suppress tumor growth with negligible systemic toxicity. To extend the comprehensive application of this strategy, interferon-γ (IFN-γ) was further introduced to the combinatorial system to develop cytokine cocktails adsorbed NVs. This kind of NVs can significantly inhibit the primary tumor growth and lung metastasis of triple-negative breast cancer. With exploration of underlying mechanism, the cytokine cocktails adsorbed NVs can facilitate maturation of dendritic cells, promote the infiltration and activation of CD8 T lymphocytes and natural killer cells, and increase the recruitment of CD45 immune cells and Ly6G neutrophils.
利用药物递送系统,可以将具有不同理化性质的免疫刺激剂和化疗药物共同递送到肿瘤部位,以实现协同的抗肿瘤效果。在这里,我们首次通过一种简单的无溶剂方法,将免疫刺激细胞因子白细胞介素-2(IL-2)高包封率地吸附到载多柔比星(DOX)的纳米囊泡(NV-DOX)中。静脉注射到荷黑色素瘤小鼠后,NV-DOX 可以在肿瘤部位积累,并显著抑制肿瘤生长,而全身毒性可忽略不计。为了扩展这种策略的综合应用,我们进一步将干扰素-γ(IFN-γ)引入到组合系统中,以开发吸附细胞因子的 NV 囊泡。这种 NV 囊泡可以显著抑制三阴性乳腺癌的原发肿瘤生长和肺转移。通过对潜在机制的探索,我们发现吸附细胞因子的 NV 囊泡可以促进树突状细胞的成熟,促进 CD8 T 淋巴细胞和自然杀伤细胞的浸润和激活,并增加 CD45 免疫细胞和 Ly6G 中性粒细胞的募集。