Nanoparticles and innate immunity: new perspectives on host defence

被引:257
作者
Boraschi, Diana [1 ]
Italiani, Paola [1 ]
Palomba, Roberto [2 ]
Decuzzi, Paolo [2 ]
Duschl, Albert [3 ]
Fadeel, Bengt [4 ]
Moghimi, S. Moein [5 ,6 ]
机构
[1] CNR, Inst Prot Biochem, Via Pietro Castellino 111, I-80131 Naples, Italy
[2] Italian Inst Technol Fdn, Lab Nanotechnol Precis Med, Via Morego 30, I-16163 Genoa, Italy
[3] Paris Lodron Univ Salzburg, Dept Mol Biol, Hellbrunner Str 34, A-5020 Salzburg, Austria
[4] Karolinska Inst, Inst Environm Med, Nanosafety & Nanomed Lab, Nobels Vag 13, S-17177 Stockholm, Sweden
[5] Univ Durham, Sch Med Pharm & Hlth, Queens Campus, Stockton On Tees TS17 6BH, England
[6] Newcastle Univ, Inst Cellular Med, Framlington Pl, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
基金
欧洲研究理事会; 欧盟地平线“2020”;
关键词
Innate immunity; Engineered nanoparticles; Inflammation; Immunosafety; Toxicity; Complement; NEUTROPHIL EXTRACELLULAR TRAPS; WALLED-CARBON-NANOTUBES; TUMOR-ASSOCIATED MACROPHAGES; NONCANONICAL INFLAMMASOME ACTIVATION; DISCOIDAL POLYMERIC NANOCONSTRUCTS; MEDIATED COMPLEMENT ACTIVATION; IRON-OXIDE NANOPARTICLES; NALP3; INFLAMMASOME; DENDRITIC CELLS; SILVER NANOPARTICLES;
D O I
10.1016/j.smim.2017.08.013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The innate immune system provides the first line of defence against foreign microbes and particulate materials. Engineered nanoparticles can interact with the immune system in many different ways. Nanoparticles may thus elicit inflammation with engagement of neutrophils, macrophages and other effector cells; however, it is important to distinguish between acute and chronic inflammation in order to identify the potential hazards of nanoparticles for human health. Nanoparticles may also interact with and become internalised by dendritic cells, key antigen-presenting cells of the immune system, where a better understanding of these processes could pave the way for improved vaccination strategies. Nanoparticle characteristics such as size, shape and deformability also influence nanoparticle uptake by a plethora of immune cells and subsequent immune responses. Furthermore, the corona of adsorbed biomolecules on nanoparticle surfaces should not be neglected. Complement activation represents a special case of regulated and dynamic corona formation on nanoparticles with important implications in clearance and safety. Additionally, the inadvertent binding of bacterial lipopolysaccharide to nanoparticles is important to consider as this may skew the outcome and interpretation of immunotoxicological studies. Here, we discuss nanoparticle interactions with different cell types and soluble mediators belonging to the innate immune system.
引用
收藏
页码:33 / 51
页数:19
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