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仿生细胞外膜纳米疫苗可长期预防乳腺癌的发生。

Biomimetic cytomembrane nanovaccines prevent breast cancer development in the long term.

机构信息

Center Laboratory, Zhangjiagang Traditional Chinese Medicine Hospital Affiliated to Nanjing University of Chinese Medicine, Zhangjiagang, Jiangsu 215600, China.

Department of Obstetrics and Gynecology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215006, China.

出版信息

Nanoscale. 2021 Feb 14;13(6):3594-3601. doi: 10.1039/d0nr08978h. Epub 2021 Feb 10.

DOI:10.1039/d0nr08978h
PMID:33564813
Abstract

Cytomembrane cancer nanovaccines are considered a promising approach to induce tumor-specific immunity. Most of the currently developed nanovaccines, unfortunately, fail to study the underlying mechanism for cancer prevention and therapy, as well as immune memory establishment, with their long-term anti-tumor immunity remaining unknown. Here, we present a strategy to prepare biomimetic cytomembrane nanovaccines (named CCMP@R837) consisting of antigenic cancer cell membrane (CCM)-capped poly(lactic-co-glycolic acid) (PLGA) nanoparticles loaded with imiquimod (R@837) as an adjuvant to activate the immune system. We found that our CCMP@R837 system enhanced bone-marrow-derived dendritic cell uptake and maturation, as well as increased anti-tumor response against breast cancer 4T1 cells in vitro. Moreover, an immune memory was established after three-time immunization with CCMP@R837 in BALB/c mice. The CCMP@R837-immunized BALB/c mice exhibited suppressed tumor growth and a long survival period (75% of mice lived longer than 50 days after tumor formation). This long-term anti-tumor immunity was achieved by increasing CD8 T cells and decreasing regulatory T cells in the tumor while increasing effector memory T cells in the spleen. Overall, our platform demonstrates that CCMP@R837 can be a potential candidate for preventive cancer vaccines in the clinic.

摘要

细胞表面膜癌症纳米疫苗被认为是一种很有前途的方法,可以诱导肿瘤特异性免疫。不幸的是,目前大多数开发的纳米疫苗都未能研究癌症预防和治疗以及免疫记忆建立的潜在机制,其长期抗肿瘤免疫仍然未知。在这里,我们提出了一种制备仿生细胞表面膜纳米疫苗(命名为 CCMP@R837)的策略,该疫苗由带抗原的癌细胞膜(CCM)封端的聚(乳酸-共-乙醇酸)(PLGA)纳米颗粒组成,负载咪喹莫特(R@837)作为佐剂来激活免疫系统。我们发现,我们的 CCMP@R837 系统增强了骨髓来源的树突状细胞的摄取和成熟,以及体外对乳腺癌 4T1 细胞的抗肿瘤反应。此外,在 BALB/c 小鼠中进行三次 CCMP@R837 免疫后建立了免疫记忆。CCMP@R837 免疫的 BALB/c 小鼠表现出抑制肿瘤生长和延长生存时间(75%的小鼠在肿瘤形成后存活超过 50 天)。这种长期的抗肿瘤免疫是通过增加肿瘤中的 CD8 T 细胞和减少调节性 T 细胞,同时增加脾脏中的效应记忆 T 细胞来实现的。总的来说,我们的平台表明 CCMP@R837 可能成为临床预防癌症疫苗的潜在候选物。

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