Department of Pharmacy and Biochemistry, Johannes Gutenberg-University Mainz , Staudingerweg 5, 55128 Mainz, Germany.
Department of Dermatology, University Medical Center, Johannes Gutenberg-University Mainz , Obere Zahlbacher Straße 63, 55131 Mainz, Germany.
Mol Pharm. 2017 Dec 4;14(12):4403-4416. doi: 10.1021/acs.molpharmaceut.7b00507. Epub 2017 Nov 8.
Surface modifications of nanoparticles can alter their physical and biological properties significantly. They effect particle aggregation, circulation times, and cellular uptake. This is particularly critical for the interaction with primary immune cells due to their important role in particle processing. We can show that the introduction of a hydrophilic PEG layer on the surface of the polysaccharide-based nanoparticles prevents unwanted aggregation under physiological conditions and decreases unspecific cell uptake in different primary immune cell types. The opposite effect can be observed with a parallel-performed introduction of a layer of low molecular weight dextran (3.5 and 5 kDa) on the particle surface (DEXylation) that encourages the nanoparticle uptake by antigen-presenting cells like macrophages and dendritic cells. Binding of DEXylated particles to these immune cells results in an upregulation of surface maturation markers and elevated production of proinflammatory cytokines, reflecting cell activation. Hence, DEXylated particles can potentially be used for passive targeting of antigen presenting cells with inherent adjuvant function for future immunotherapeutic applications.
纳米粒子的表面修饰可以显著改变其物理和生物特性。它们影响颗粒的聚集、循环时间和细胞摄取。由于初级免疫细胞在颗粒处理中起着重要作用,因此这对于与初级免疫细胞的相互作用尤为关键。我们可以证明,在多糖基纳米粒子表面引入亲水性 PEG 层可以防止在生理条件下发生不必要的聚集,并减少不同原发性免疫细胞类型中非特异性的细胞摄取。在平行引入低分子量葡聚糖(3.5 和 5 kDa)层(DEXylation)时可以观察到相反的效果,这会促进抗原呈递细胞(如巨噬细胞和树突状细胞)摄取纳米颗粒。DEXylated 颗粒与这些免疫细胞的结合导致表面成熟标志物的上调和促炎细胞因子的产生增加,反映了细胞的激活。因此,DEXylated 颗粒可能可用于未来免疫治疗应用中具有固有佐剂功能的抗原呈递细胞的被动靶向。