McCarthy Derrick P, Hunter Zoe N, Chackerian Bryce, Shea Lonnie D, Miller Stephen D
Department of Microbiology-Immunology and Interdepartmental Immunobiology Center, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2014 May-Jun;6(3):298-315. doi: 10.1002/wnan.1263. Epub 2014 Mar 10.
The growing prevalence of nanotechnology in the fields of biology, medicine, and the pharmaceutical industry is confounded by the relatively small amount of data on the impact of these materials on the immune system. In addition to concerns surrounding the potential toxicity of nanoparticle (NP)-based delivery systems, there is also a demand for a better understanding of the mechanisms governing interactions of NPs with the immune system. Nanoparticles can be tailored to suppress, enhance, or subvert recognition by the immune system. This 'targeted immunomodulation' can be achieved by delivery of unmodified particles, or by modifying particles to deliver drugs, proteins/peptides, or genes to a specific site. In order to elicit the desired, beneficial immune response, considerations should be made at every step of the design process: the NP platform itself, ligands, and other modifiers, the delivery route, and the immune cells that will encounter the conjugated NPs can all impact host immune responses.
纳米技术在生物学、医学和制药行业领域的日益普及,与这些材料对免疫系统影响的数据相对较少形成了矛盾。除了对基于纳米颗粒(NP)的递送系统潜在毒性的担忧外,人们还要求更好地理解控制纳米颗粒与免疫系统相互作用的机制。纳米颗粒可以进行定制,以抑制、增强或颠覆免疫系统的识别。这种“靶向免疫调节”可以通过递送未修饰的颗粒来实现,或者通过修饰颗粒以将药物、蛋白质/肽或基因递送至特定部位来实现。为了引发期望的有益免疫反应,在设计过程的每个步骤都应予以考虑:NP平台本身、配体和其他修饰剂、递送途径以及将遇到缀合纳米颗粒的免疫细胞,所有这些都会影响宿主免疫反应。