Cytokines as biomarkers of nanoparticle immunotoxicity

被引:304
作者
Elsabahy, Mahmoud [1 ,2 ,3 ,4 ]
Wooley, Karen L. [1 ,2 ,3 ]
机构
[1] Texas A&M Univ, Dept Chem, College Stn, TX 77842 USA
[2] Texas A&M Univ, Dept Chem Engn, College Stn, TX 77842 USA
[3] Texas A&M Univ, Lab Synthet Biol Interact, College Stn, TX 77842 USA
[4] Assiut Univ, Al Rajhy Liver Hosp, Fac Pharm, Assiut Int Ctr Nanomed,Dept Pharmaceut, Assiut, Egypt
基金
美国国家卫生研究院;
关键词
WALLED-CARBON-NANOTUBES; CELLS IN-VITRO; TITANIUM-DIOXIDE NANOPARTICLES; MONOCLONAL-ANTIBODY TGN1412; CROSS-LINKED NANOPARTICLES; QUANTUM-DOT NANOPARTICLES; BLOCK-COPOLYMER MICELLES; ANTIGEN-PRESENTING CELLS; INNATE IMMUNE-RESPONSE; LUNG EPITHELIAL-CELLS;
D O I
10.1039/c3cs60064e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanoscale objects, whether of biologic origin or synthetically created, are being developed into devices for a variety of bionanotechnology diagnostic and pharmaceutical applications. However, the potential immunotoxicity of these nanomaterials and mechanisms by which they may induce adverse reactions have not received sufficient attention. Nanomaterials, depending on their characteristics and compositions, can interact with the immune system in several ways and either enhance or suppress immune system function. Cytokines perform pleiotropic functions to mediate and regulate the immune response and are generally recognized as biomarkers of immunotoxicity. While the specificity and validity of certain cytokines as markers of adverse immune response has been established for chemicals, small and macromolecular drugs, research on their applicability for predicting and monitoring the immunotoxicity of engineered nanomaterials is still ongoing. The goal of this review is to provide guidelines as to important cytokines that can be utilized for evaluating the immunotoxicity of nanomaterials and to highlight the role of those cytokines in mediating adverse reactions, which is of particular importance for the clinical development of nanopharmaceuticals and other nanotechnology-based products. Importantly, the rational design of nanomaterials of low immunotoxicity will be discussed, focusing on synthetic nanodevices, with emphasis on both the nanoparticle-forming materials and the embedded cargoes.
引用
收藏
页码:5552 / 5576
页数:25
相关论文
共 205 条
[31]   Preclinical studies to understand nanoparticle interaction with the immune system and its potential effects on nanoparticle biodistribution [J].
Dobrovolskaia, Marina A. ;
Aggarwal, Parag ;
Hall, Jennifer B. ;
McNeil, Scott E. .
MOLECULAR PHARMACEUTICS, 2008, 5 (04) :487-495
[32]   Immunological properties of engineered nanomaterials [J].
Dobrovolskaia, Marina A. ;
Mcneil, Scott E. .
NATURE NANOTECHNOLOGY, 2007, 2 (08) :469-478
[33]  
Dobrovolskaia MA, 2010, NANOMEDICINE-UK, V5, P555, DOI [10.2217/nnm.10.29, 10.2217/NNM.10.29]
[34]  
Dobrovolskaia MA, 2009, NAT NANOTECHNOL, V4, P411, DOI [10.1038/nnano.2009.175, 10.1038/NNANO.2009.175]
[35]   Cysteine proteinase type I, encapsulated in solid lipid nanoparticles induces substantial protection against Leishmania major infection in C57BL/6 mice [J].
Doroud, D. ;
Zahedifard, F. ;
Vatanara, A. ;
Najafabadi, A. R. ;
Rafati, S. .
PARASITE IMMUNOLOGY, 2011, 33 (06) :335-348
[36]   Beating cancer in multiple ways using nanogold [J].
Dreaden, Erik C. ;
Mackey, Megan A. ;
Huang, Xiaohua ;
Kang, Bin ;
El-Sayed, Mostafa A. .
CHEMICAL SOCIETY REVIEWS, 2011, 40 (07) :3391-3404
[37]   Impact of Nanoparticles on the Immune System [J].
Dwivedi, Premendra D. ;
Tripathi, Anurag ;
Ansari, Kausar M. ;
Shanker, Rishi ;
Das, Mukul .
JOURNAL OF BIOMEDICAL NANOTECHNOLOGY, 2011, 7 (01) :193-194
[38]   Strategies toward well-defined polymer nanoparticles inspired by nature: Chemistry versus versatility [J].
Elsabahy, Mahmoud ;
Wooley, Karen L. .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2012, 50 (10) :1869-1880
[39]   Design of polymeric nanoparticles for biomedical delivery applications [J].
Elsabahy, Mahmoud ;
Wooley, Karen L. .
CHEMICAL SOCIETY REVIEWS, 2012, 41 (07) :2545-2561
[40]  
Elsabahy M, 2010, PAN ST SER BIOM NANO, V1, P169