趋化因子负载脂质体的体外表征。

Cogent Biology Pub Date : 2019-01-01 Epub Date: 2019-09-11 DOI:10.1080/23312025.2019.1662931
Angel J Rubio, Xuemei Zhong, Tyrone M Porter
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引用次数: 1

摘要

最近出现的免疫疗法正在改变癌症治疗。尽管许多癌症免疫疗法在治疗血液学肿瘤方面取得了巨大的成功,但治疗实体肿瘤的一个主要障碍是将免疫细胞定位到肿瘤部位。因此,我们开发了一种能够引导免疫细胞迁移的技术。具体来说,我们在聚乙二醇修饰脂质体中包装了趋化因子,即促进免疫细胞迁移的信号分子。在含血清的培养基中检测了脂质体中趋化因子和其他大分子的释放谱。我们已经证明脂质体能够释放趋化因子来诱导免疫细胞迁移。此外,这些脂质体已在体外通过增加免疫细胞募集来限制癌细胞的生长。这种在脂质体内封装趋化因子的策略为额外的癌症免疫疗法和基于趋化因子的疗法铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

In vitro characterization of chemokine-loaded liposomes.

In vitro characterization of chemokine-loaded liposomes.

In vitro characterization of chemokine-loaded liposomes.

In vitro characterization of chemokine-loaded liposomes.

The recent emergence of immunotherapies is transforming cancer treatments. Although many cancer immunotherapies are finding enormous success for treating hematologic tumors, a major obstacle for the treatment of solid tumors is localizing immune cells to the tumor site. Therefore, we have developed a technology that is capable of directing immune cell migration. Specifically, we have packaged chemokines, signaling molecules that promote immune cell migration, inside polyethylene glycol decorated-liposomes. The release profiles of chemokines and other large molecules from the liposomes have been examined in serum-containing media. We have demonstrated that the liposomes are able to release chemokines to induce immune cell migration. Additionally, these liposomes have been shown in vitro to limit cancer cell growth through increased immune cell recruitment. This strategy of encapsulating chemokines within liposomes paves the way for additional cancer immunotherapies and chemokine-based therapies.

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Cogent Biology
Cogent Biology MULTIDISCIPLINARY SCIENCES-
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