趋化因子和纳米材料:用于免疫应用的相互作用

G. Bardi
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引用次数: 1

摘要

趋化因子是调节免疫细胞迁移的稳态或炎性小蛋白,其结构特征为半胱氨酸二硫桥。已发现约50种人类趋化因子结合近20种七跨膜g蛋白偶联受体。发现其中两种是人类免疫缺陷病毒(HIV)的主要共受体,加强了对阻断病毒进入的结合机制的研究。趋化因子/趋化因子受体信号的阻断最终调节细胞迁移,进而调节免疫应答。可以设计特定的纳米技术来干扰趋化因子信号传导或利用配体-受体相互作用。用趋化因子或特定肽对纳米材料进行表面化学修饰可以在生物医学中找到几种应用,从组织特异性药物递送到病理条件下减少细胞迁移。将讨论最近在特殊趋化因子纳米颗粒设计及其调节免疫反应的潜力方面的亮点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chemokines and nanomaterials: interaction for useful immune-applications
Chemokines are homeostatic or inflammatory small proteins regulating immune cell migration and are structurally characterized by cysteine disulfide bridges. Around 50 human chemokines binding almost 20 seven-transmembrane G-protein coupled receptors have been discovered. The finding that two of them were the main human immunodeficiency virus (HIV) co-receptors intensified the research on the binding mechanism to block the viral entrance. Blockade of chemokine/chemokine receptor signaling ultimately modulates cell migration, then immune responses. Particular nanotechnologies can be designed to interfere with chemokine signaling or to exploit the ligand-receptor interaction. Surface chemical modification of nanomaterials with chemokines or specific peptides can find several applications in bio-medicine, from tissue-specific drug delivery to reduced cell migration in pathological conditions. Recent highlights on peculiar chemokine-nanoparticle design and their potential to modulate immune responses will be discussed.
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