Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, MD. 21231.
Translational Tissue Engineering Center, Johns Hopkins University School of Medicine, Baltimore, MD. 21231.
Biomaterials. 2014 Jan;35(1):269-277. doi: 10.1016/j.biomaterials.2013.09.050. Epub 2013 Oct 5.
Previous work developing particle-based acellular, artificial antigen presenting cells (aAPCs) has focused exclusively on spherical platforms. To explore the role of shape, we generated ellipsoidal PLGA microparticles with varying aspect ratios (ARs) and synthesized aAPCs from them. The ellipsoidal biomimetic aAPCs with high-AR showed significantly enhanced in vitro and in vivo activity above spherical aAPCs with particle volume and antigen content held constant. Confocal imaging indicates that CD8+ T cells preferentially migrate to and are activated by interaction with the long axis of the aAPC. Importantly, enhanced activity of high-AR aAPCs was seen in a mouse melanoma model, with high-AR aAPCs improving melanoma survival compared to non-cognate aAPCs (p = 0.004) and cognate spherical aAPCs (p = 0.05). These findings indicate that particle geometry is a critical design criterion in the generation of aAPCs, and may offer insight into the essential role of geometry in the interaction between CD8+ T cells and biological APCs.
先前开发基于颗粒的无细胞人工抗原呈递细胞(aAPC)的工作仅专注于球形平台。为了探索形状的作用,我们生成了具有不同纵横比(AR)的椭圆形 PLGA 微球,并从它们中合成了 aAPC。在保持颗粒体积和抗原含量不变的情况下,具有高 AR 的椭圆形仿生 aAPC 的体外和体内活性明显高于球形 aAPC。共聚焦成像表明,CD8+T 细胞优先迁移并通过与 aAPC 的长轴相互作用而被激活。重要的是,在小鼠黑色素瘤模型中观察到高 AR aAPC 的活性增强,与非同源 aAPC(p=0.004)和同源球形 aAPC(p=0.05)相比,高 AR aAPC 提高了黑色素瘤的存活率。这些发现表明,颗粒几何形状是 aAPC 产生的关键设计标准,并可能深入了解 CD8+T 细胞与生物 APC 相互作用中几何形状的重要作用。