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Nanoparticles and innate immunity: new perspectives on host defence

Boraschi, Diana, Italiani, Paola, Palomba, Roberto, Decuzzi, Paolo, Duschl, Albert, Fadeel, Bengt, Moghimi, S. Moein·2017·Seminars in Immunology

Abstract

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.

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Research works printed but not linked: 230

  1. Boraschi, 2016, Interaction between the immune system and nanomaterials: safety and medical exploitation, Curr. Bionanotechnol., 2, 3, 10.2174/221352940201160718174904 · DOI
  2. Shvedova, 2010, Close encounters of the small kind: adverse effects of man-made materials interfacing with the nano-cosmos of biological systems, Ann. Rev. Pharmacol. Toxicol., 50, 63, 10.1146/annurev.pharmtox.010909.105819 · DOI
  3. Zahr, 2006, Macrophage uptake of core-shell nanoparticles surface modified with poly(ethylene glycol), Langmuir, 22, 8178, 10.1021/la060951b · DOI
  4. Dobrovolskaia, 2007, Immunological properties of engineered nanomaterials, Nat. Nanotechnol., 2, 469, 10.1038/nnano.2007.223 · DOI · Paper page
  5. Aggarwal, 2009, Nanoparticle interaction with plasma proteins as it relates to particle biodistribution, biocompatibility and therapeutic efficacy, Adv. Drug Deliv. Rev., 61, 428, 10.1016/j.addr.2009.03.009 · DOI · Paper page
  6. Fang, 2006, In vivo tumor targeting of tumor necrosis factor alpha-loaded stealth nanoparticles: effect of MePEG molecular weight and particle size, Eur. J. Pharm. Sci., 27, 27, 10.1016/j.ejps.2005.08.002 · DOI
  7. Mahon, 2012, Designing the nanoparticle-biomolecule interface for targeting and therapeutic delivery, J. Controlled Release, 161, 164, 10.1016/j.jconrel.2012.04.009 · DOI
  8. Monopoli, 2013, Formation and characterization of the nanoparticle protein corona, Methods Mol. Biol., 1025, 137, 10.1007/978-1-62703-462-3_11 · DOI
  9. Esmaeili, 2008, PLGA nanoparticles of different surface properties: preparation and evaluation of their body distribution, Int. J. Pharm., 349, 249, 10.1016/j.ijpharm.2007.07.038 · DOI · Paper page
  10. Fleischer, 2012, Nanoparticle surface charge mediates the cellular receptors used by protein-nanoparticle complexes, J. Phys. Chem. B, 116, 8901, 10.1021/jp304630q · DOI
  11. Moghimi, 1993, Coating particles with a block co-polymer (poloxamine-908) suppresses opsonization but permits the activity of dysopsonins in the serum, Biochim. Biophys. Acta, 1179, 157, 10.1016/0167-4889(93)90137-E · DOI
  12. Oostingh, 2011, Problems and challenges in the development and validation of human cell-based assays to determine nanoparticle-induced immunomodulatory effects, Part. Fibre Toxicol., 8, 8, 10.1186/1743-8977-8-8 · DOI
  13. Krug, 2014, Nanosafety research – are we on the right track? Some thoughts based on a comprehensive literature review, Angew. Chem. Int. Ed., 53, 12304, 10.1002/anie.201403367 · DOI
  14. Li, 2016, Endotoxin contamination: a key element in the interpretation of nanosafety studies, Nanomed. Future Med., 11, 269
  15. Li, 2017, Endotoxin contamination in nanomaterials leads to the misinterpretation of immunosafety results, Front. Immunol., 8, 472, 10.3389/fimmu.2017.00472 · DOI · Paper page
  16. Li, 2015, Optimising the use of commercial LAL assays for the analysis of endotoxin contamination in metal colloids and metal oxide nanoparticles, Nanotoxicology, 9, 462, 10.3109/17435390.2014.948090 · DOI
  17. Schwarz, 2017, Biological activity of masked endotoxin, Sci. Rep., 7, 44750, 10.1038/srep44750 · DOI
  18. Mukherjee, 2016, Detection of endotoxin contamination of graphene based materials using the TNF-α expression test and guidelines for endotoxin-free graphene oxide production, PLoS One, 11, e0166816, 10.1371/journal.pone.0166816 · DOI
  19. Schwarz, 2014, Residual endotoxin contaminations in recombinant proteins are sufficient to activate human CD1c+ dendritic cells, PLoS One, 9, e113840, 10.1371/journal.pone.0113840 · DOI
  20. Li, 2016, Assessing the immunosafety of engineered nanoparticles with a novel in vitro model based on human primary monocytes, ACS Appl. Mater. Interfaces
  21. Triantafilou, 2002, Lipopolysaccharide recognition: CD14 TLRs and the LPS-activation cluster, Trends Immunol., 23, 301, 10.1016/S1471-4906(02)02233-0 · DOI
  22. Kayagaki, 2013, Noncanonical inflammasome activation by intracellular LPS independent of TLR4, Science, 341, 1246, 10.1126/science.1240248 · DOI
  23. Hagar, 2013, Cytoplasmic LPS activates caspase-11: implications in TLR4-independent endotoxic shock, Science, 341, 1250, 10.1126/science.1240988 · DOI
  24. Opal, 2013, Effect of eritoran, an antagonist of MD2-TLR4, on mortality in patients with severe sepsis: the ACCESS randomized trial, JAMA, 309, 1154, 10.1001/jama.2013.2194 · DOI · Paper page
  25. Martinon, 2004, Inflammatory caspases: linking an intracellular innate immune system to autoinflammatory diseases, Cell, 117, 561, 10.1016/j.cell.2004.05.004 · DOI
  26. Fadeel, 2012, Clear and present danger? Engineered nanoparticles and the immune system, Swiss Med. Wkly., 142, w13609, 10.4414/smw.2012.13609 · DOI
  27. Broz, 2016, Inflammasomes: mechanism of assembly, regulation and signalling, Nat. Rev. Immunol., 16, 407, 10.1038/nri.2016.58 · DOI · Paper page
  28. Farrera, 2015, It takes two to tango: understanding the interactions between engineered nanomaterials and the immune system, Eur. J. Pharm. Biopharm., 95A, 3, 10.1016/j.ejpb.2015.03.007 · DOI · Paper page
  29. Bhattacharya, 2013, Mechanisms of carbon nanotube-induced toxicity: focus on pulmonary inflammation, Adv. Drug Deliv. Rev., 65, 2087, 10.1016/j.addr.2013.05.012 · DOI
  30. Braakhuis, 2014, Physicochemical characteristics of nanomaterials that affect pulmonary inflammation, Part. Fibre Toxicol., 11, 18, 10.1186/1743-8977-11-18 · DOI
  31. Landsiedel, 2014, Pulmonary toxicity of nanomaterials: a critical comparison of published in vitro assays and in vivo inhalation or instillation studies, Nanomedicine (Lond.), 9, 2557, 10.2217/nnm.14.149 · DOI
  32. Cho, 2010, Metal oxide nanoparticles induce unique inflammatory footprints in the lung: important implications for nanoparticle testing, Environ. Health Perspect., 118, 1699, 10.1289/ehp.1002201 · DOI
  33. Cho, 2012, Differential pro-inflammatory effects of metal oxide nanoparticles and their soluble ions in vitro and in vivo; zinc and copper nanoparticles, but not their ions, recruit eosinophils to the lungs, Nanotoxicology, 6, 22, 10.3109/17435390.2011.552810 · DOI
  34. Gustafsson, 2011, Lung exposure of titanium dioxide nanoparticles induces innate immune activation and long-lasting lymphocyte response in the Dark Agouti rat, J. Immunotoxicol., 8, 111, 10.3109/1547691X.2010.546382 · DOI
  35. Scoville, 2015, Susceptibility to quantum dot induced lung inflammation differs widely among the collaborative cross founder mouse strains, Toxicol. Appl. Pharmacol., 289, 240, 10.1016/j.taap.2015.09.019 · DOI
  36. Gustafsson, 2015, Differential cellular responses in healthy mice and in mice with established airway inflammation when exposed to hematite nanoparticles, Toxicol. Appl. Pharmacol., 288, 1, 10.1016/j.taap.2015.07.001 · DOI
  37. Rossi, 2015, Inhalation exposure to nanosized and fine TiO2 particles inhibits features of allergic asthma in a murine model, Part. Fibre Toxicol., 7, 35, 10.1186/1743-8977-7-35 · DOI
  38. Donaldson, 2013, Pulmonary toxicity of carbon nanotubes and asbestos – similarities and differences, Adv. Drug Deliv. Rev., 65, 2078, 10.1016/j.addr.2013.07.014 · DOI
  39. Shvedova, 2005, Unusual inflammatory and fibrogenic pulmonary responses to single-walled carbon nanotubes in mice, Am. J. Physiol. Lung Cell. Mol. Physiol., 289, L698, 10.1152/ajplung.00084.2005 · DOI · Paper page
  40. Shvedova, 2008, Inhalation vs. aspiration of single-walled carbon nanotubes in C57BL/6 mice: inflammation, fibrosis, oxidative stress, and mutagenesis, Am. J. Physiol. Lung Cell. Mol. Physiol., 295, L552, 10.1152/ajplung.90287.2008 · DOI
  41. Poland, 2008, Carbon nanotubes introduced into the abdominal cavity of mice show asbestos-like pathogenicity in a pilot study, Nat. Nanotechnol., 3, 423, 10.1038/nnano.2008.111 · DOI · Paper page
  42. Rydman, 2014, Inhalation of rod-like carbon nanotubes causes unconventional allergic airway inflammation, Part. Fibre Toxicol., 11, 48, 10.1186/s12989-014-0048-2 · DOI
  43. Katwa, 2012, A carbon nanotube toxicity paradigm driven by mast cells and the IL-33/ST2 axis, Small, 8, 2904, 10.1002/smll.201200873 · DOI
  44. Cassel, 2008, The Nalp3 inflammasome is essential for the development of silicosis, Proc. Natl. Acad. Sci. U. S. A., 105, 9035, 10.1073/pnas.0803933105 · DOI · Paper page
  45. Sun, 2013, NLRP3 inflammasome activation induced by engineered nanomaterials, Small, 9, 1595, 10.1002/smll.201201962 · DOI
  46. Muñoz-Planillo, 2013, K+ efflux is the common trigger of NLRP3 inflammasome activation by bacterial toxins and particulate matter, Immunity, 38, 1142, 10.1016/j.immuni.2013.05.016 · DOI
  47. Li, 2014, Surface interactions with compartmentalized cellular phosphates explain rare earth oxide nanoparticle hazard and provide opportunities for safer design, ACS Nano, 8, 1771, 10.1021/nn406166n · DOI
  48. Tsugita, 2017, SR-B1 is a silica receptor that mediates canonical inflammasome activation, Cell Rep., 18, 1298, 10.1016/j.celrep.2017.01.004 · DOI
  49. Andón, 2013, Programmed cell death: molecular mechanisms and implications for safety assessment of nanomaterials, Acc. Chem. Res., 46, 733, 10.1021/ar300020b · DOI
  50. Bergsbaken, 2009, Pyroptosis: host cell death and inflammation, Nat. Rev. Microbiol., 7, 99, 10.1038/nrmicro2070 · DOI
  51. Shi, 2015, Cleavage of GSDMD by inflammatory caspases determines pyroptotic cell death, Nature, 526, 660, 10.1038/nature15514 · DOI · Paper page
  52. Reisetter, 2011, Induction of inflammasome-dependent pyroptosis by carbon black nanoparticles, J. Biol. Chem., 286, 21844, 10.1074/jbc.M111.238519 · DOI
  53. Andón, 2017, Hollow carbon spheres trigger inflammasome-dependent IL-1β secretion in macrophages, Carbon, 113, 243, 10.1016/j.carbon.2016.11.049 · DOI
  54. Chen, 2016, The murine neutrophil NLRP3 inflammasome is activated by soluble but not particulate or crystalline agonists, Eur. J. Immunol., 46, 1004, 10.1002/eji.201545943 · DOI
  55. Chen, 2014, The neutrophil NLRC4 inflammasome selectively promotes IL-1β maturation without pyroptosis during acute Salmonella challenge, Cell Rep., 8, 570, 10.1016/j.celrep.2014.06.028 · DOI
  56. Branzk, 2014, Neutrophils sense microbe size and selectively release neutrophil extracellular traps in response to large pathogens, Nat. Immunol., 15, 1017, 10.1038/ni.2987 · DOI · Paper page
  57. Liz, 2015, Silver nanoparticles rapidly induce atypical human neutrophil cell death by a process involving inflammatory caspases and reactive oxygen species and induce neutrophil extracellular traps release upon cell adhesion, Int. Immunopharmacol., 28, 616, 10.1016/j.intimp.2015.06.030 · DOI
  58. Hwang, 2015, The impact of cationic solid lipid nanoparticles on human neutrophil activation and formation of neutrophil extracellular traps (NETs), Chem. Biol. Interact., 235, 106, 10.1016/j.cbi.2015.04.011 · DOI
  59. Muñoz, 2016, Nanoparticles size-dependently initiate self-limiting NETosis-driven inflammation, Proc. Natl. Acad. Sci. U. S. A., 113, E5856, 10.1073/pnas.1602230113 · DOI
  60. Farrera, 2014, Extracellular entrapment and degradation of single-walled carbon nanotubes, Nanoscale, 6, 6974, 10.1039/c3nr06047k · DOI
  61. Mukherjee, 2017, Graphene and the immune system: a romance of many dimensions, Front. Immunol., 8, 673, 10.3389/fimmu.2017.00673 · DOI
  62. Grosse, 2014, Carcinogenicity of fluoro-edenite, silicon carbide fibres and whiskers, and carbon nanotubes, Lancet Oncol., 15, 1427, 10.1016/S1470-2045(14)71109-X · DOI
  63. Vlasova, 2016, Enzymatic oxidative biodegradation of nanoparticles: mechanisms, significance and applications, Toxicol. Appl. Pharmacol., 299, 58, 10.1016/j.taap.2016.01.002 · DOI
  64. Russier, 2011, Oxidative biodegradation of single- and multi-walled carbon nanotubes, Nanoscale, 3, 893, 10.1039/C0NR00779J · DOI
  65. Kagan, 2010, Carbon nanotubes degraded by neutrophil myeloperoxidase induce less pulmonary inflammation, Nat. Nanotechnol., 5, 354, 10.1038/nnano.2010.44 · DOI
  66. Shvedova, 2012, Impaired clearance and enhanced pulmonary inflammatory/fibrotic response to carbon nanotubes in myeloperoxidase-deficient mice, PLoS One, 7, e30923, 10.1371/journal.pone.0030923 · DOI
  67. Andón, 2013, Biodegradation of single-walled carbon nanotubes by eosinophil peroxidase, Small, 9, 2721, 10.1002/smll.201202508 · DOI
  68. Sureshbabu, 2015, Degradation-by-design: surface modification with functional substrates that enhance the enzymatic degradation of carbon nanotubes, Biomaterials, 72, 20, 10.1016/j.biomaterials.2015.08.046 · DOI
  69. Italiani, 2014, From monocytes to M1/M2 macrophages: phenotypical vs. functional differentiation, Front. Immunol., 5, 514, 10.3389/fimmu.2014.00514 · DOI · Paper page
  70. Gordon, 2014, Macrophage heterogeneity in tissues: phenotypic diversity and functions, Immunol. Rev., 262, 36, 10.1111/imr.12223 · DOI
  71. Ginhoux, 2016, Tissue-resident macrophage ontogeny and homeostasis, Immunity, 44, 439, 10.1016/j.immuni.2016.02.024 · DOI · Paper page
  72. Fejer, 2015, Self-renewing macrophages–a new line of enquiries in mononuclear phagocytes, Immunobiology, 220, 169, 10.1016/j.imbio.2014.11.005 · DOI
  73. Martinez, 2011, Regulators of macrophage activation, Eur. J. Immunol., 41, 1531, 10.1002/eji.201141670 · DOI
  74. Mantovani, 2002, Macrophage polarization: tumor-associated macrophages as a paradigm for polarized M2 mononuclear phagocytes, Trends Immunol., 23, 549, 10.1016/S1471-4906(02)02302-5 · DOI · Paper page
  75. Brown, 2017, The promise of targeting macrophages in cancer therapy, Clin. Cancer Res., 23, 3241, 10.1158/1078-0432.CCR-16-3122 · DOI
  76. Hoppstädter, 2015, M2 polarization enhances silica nanoparticle uptake by macrophages, Front. Pharmacol., 6, 55, 10.3389/fphar.2015.00055 · DOI
  77. Miao, 2017, The current state of nanoparticle-induced macrophage polarization and reprogramming research, Int. J. Mol. Sci., 18, 10.3390/ijms18020336 · DOI
  78. Yen, 2009, Cytotoxicity and immunological response of gold and silver nanoparticles of different sizes, Small, 5, 1553, 10.1002/smll.200900126 · DOI
  79. Nishanth, 2011, Inflammatory responses of RAW264.7 macrophages upon exposure to nanoparticles: role of ROS-NFkB signaling pathway, Nanotoxicology, 5, 502, 10.3109/17435390.2010.541604 · DOI · Paper page
  80. Hashimoto, 2014, Responses of RAW264.7 macrophages to water-dispersible gold and silver nanoparticles stabilized by metal-carbon sigma-bonds, J. Biomed. Mater. Res. A, 102, 1838, 10.1002/jbm.a.34854 · DOI
  81. Zhang, 2011, Uptake of gold nanoparticles in murine macrophage cells without cytotoxicity or production of pro-inflammatory mediators, Nanotoxicity, 5, 284, 10.3109/17435390.2010.512401 · DOI
  82. Giovanni, 2015, Pro-inflammatory responses of RAW264.7 macrophages when treated with ultralow concentrations of silver titanium dioxide, and zinc oxide nanoparticles, J. Hazard. Mater., 297, 146, 10.1016/j.jhazmat.2015.04.081 · DOI
  83. Zanganeh, 2016, Iron oxide nanoparticles inhibit tumour growth by inducing pro-inflammatory macrophage polarization in tumour tissues, Nat. Nanotechnol., 11, 986, 10.1038/nnano.2016.168 · DOI · Paper page
  84. Lucarelli, 2004, Innate defence functions of macrophages can be biased by nano-sized ceramic and metallic particles, Eur. Cytokine Netw., 15, 339
  85. Ma, 2015, Crucial role of lateral size for graphene oxide in activating macrophages and stimulating pro-inflammatory responses in cells and animals, ACS Nano, 9, 10498, 10.1021/acsnano.5b04751 · DOI
  86. Gallud, 2017, Macrophage activation status determines the internalization of mesoporous silica particles of different sizes: exploring the role of different pattern recognition receptors, Biomaterials, 121, 28, 10.1016/j.biomaterials.2016.12.029 · DOI
  87. Jones, 2013, Nanoparticle clearance is governed by Th1/Th2 immunity and strain background, J. Clin. Invest., 123, 3061, 10.1172/JCI66895 · DOI
  88. MacParland, 2017, Phenotype determines nanoparticle uptake by human macrophages from liver and blood, ACS Nano, 11, 2428, 10.1021/acsnano.6b06245 · DOI
  89. Laskar, 2013, SPION primes THP1 derived M2 macrophages towards M1-like macrophages, Biochem. Biophys. Res. Commun., 441, 737, 10.1016/j.bbrc.2013.10.115 · DOI · Paper page
  90. Su, 2015, Glycocalyx-mimicking nanoparticles for stimulation and polarization of macrophages via specific interactions, Small, 11, 4191, 10.1002/smll.201403838 · DOI
  91. Perisé-Barrios, 2015, Use of carbosilane dendrimer to switch macrophage polarization for the acquisition of antitumor functions, Nanoscale, 7, 3857, 10.1039/C4NR04038D · DOI
  92. Kwon, 2017, Extra-large pore mesoporous silica nanoparticles for directing in vivo M2 macrophage polarization by delivering IL-4, Nano Lett., 17, 2747, 10.1021/acs.nanolett.6b04130 · DOI
  93. Tran, 2015, Modulation of macrophage functional polarity towards anti-inflammatory phenotype with plasmid DNA delivery in CD44 targeting hyaluronic acid nanoparticles, Sci. Rep., 5, 16632, 10.1038/srep16632 · DOI
  94. Tran, 2016, MicroRNA-223 induced repolarization of peritoneal macrophages using CD44 targeting hyaluronic acid nanoparticles for anti-inflammatory effects, PLoS One, 11, e152024, 10.1371/journal.pone.0152024 · DOI
  95. Binnemars-Postma, 2017, Nanomedicine strategies to target tumor-associated macrophages, Int. J. Mol. Sci., 18, 10.3390/ijms18050979 · DOI
  96. Leonard, 2017, Macrophage polarization contributes to the anti-tumoral efficacy of mesoporous nanovectors loaded with albumin-bound paclitaxel, Front. Immunol., 8, 693, 10.3389/fimmu.2017.00693 · DOI
  97. Espinas, 2016, Epigenetic control of defense signaling and priming in plants, Front. Plant Sci., 7, 1201, 10.3389/fpls.2016.01201 · DOI
  98. Kurtz, 2005, Specific memory within innate immune systems, Trends Immunol., 26, 186, 10.1016/j.it.2005.02.001 · DOI
  99. Carriere, 2017, Impact of nanoparticles on DNA repair processes: current knowledge and working hypotheses, Mutagenesis, 32, 203, 10.1093/mutage/gew052 · DOI
  100. Durnev, 2008, Toxicology of nanoparticles, Bull. Exp. Biol. Med., 145, 72, 10.1007/s10517-008-0005-x · DOI
  101. Singh, 2009, NanoGenotoxicology: the DNA damaging potential of engineered nanomaterials, Biomaterials, 28, 2946
  102. Mytych, 2013, Nanoparticle technology as a double-edged sword: cytotoxic, genotoxic and epigenetic effects on living cells, J. Biomater. Nanobiotechnol., 4, 53, 10.4236/jbnb.2013.41008 · DOI
  103. Yao, 2013, Genetic and epigenetic effects of nanoparticles, J. Mol. Genet. Med., 7, 86
  104. Sierra, 2016, The effect of exposure to nanoparticles and nanomaterials on the mammalian epigenome, Int. J. Nanomed., 11, 6297, 10.2147/IJN.S120104 · DOI
  105. Stoccoro, 2013, Epigenetic effects of nano-sized materials, Toxicology, 313, 3, 10.1016/j.tox.2012.12.002 · DOI
  106. Conroy, 2008, CdTe nanoparticles display tropism to core histones and histone-rich cell organelles, Small, 4, 2006, 10.1002/smll.200800088 · DOI
  107. Lu, 2016, Short-term exposure to engineered nanomaterials affects cellular epigenome, Nanotoxicology, 10, 140
  108. Madrigano, 2011, Prolonged exposure to particulate pollution genes associated with glutathione pathways, and DNA methylation in a cohort of older men, Environ. Health Perspect., 119, 977, 10.1289/ehp.1002773 · DOI
  109. Bind, 2012, Air pollution and markers of coagulation inflammation, and endothelial function: associations and epigene-environment interactions in an elderly cohort, Epidemiology, 23, 332, 10.1097/EDE.0b013e31824523f0 · DOI
  110. Italiani, 2017, Induction of innate immune memory by engineered nanoparticles: a hypothesis that may become true, Front. Immunol., 8, 734, 10.3389/fimmu.2017.00734 · DOI
  111. Chiariotti, 2016, Epigenetic alterations induced by bacterial lipopolysaccharides, Adv. Exp. Med. Biol., 879, 91, 10.1007/978-3-319-24738-0_5 · DOI
  112. Milling, 2017, Delivering safer immunotherapies for cancer, Adv. Drug Deliv. Rev., 10.1016/j.addr.2017.05.011 · DOI
  113. Velpurisiva, 2017, Nanoparticle design strategies for effective cancer immunotherapy, J. Biomed. (Syd.), 2, 64, 10.7150/jbm.18877 · DOI
  114. Dimitriou, 2017, Gold nanoparticles, radiations and the immune system: current insights into the physical mechanisms and the biological interactions of this new alliance towards cancer therapy, Pharmacol. Ther., 10.1016/j.pharmthera.2017.03.006 · DOI
  115. Gutjahr, 2016, Triggering intracellular receptors for vaccine adjuvantation, Trends Immunol., 37, 573, 10.1016/j.it.2016.07.001 · DOI
  116. Taki, 2015, Small wonders-the use of nanoparticles for delivering antigen, Vaccines (Basel), 3, 638, 10.3390/vaccines3030638 · DOI
  117. Boraschi, 2015, From antigen delivery system to adjuvanticy: the board application of nanoparticles in vaccinology, Vaccines (Basel), 3, 930, 10.3390/vaccines3040930 · DOI
  118. Steinhagen, 2016, IRF5 and IRF8 modulate the CAL-1 human plasmacytoid dendritic cell line response following TLR9 ligation, Eur. J. Immunol., 46, 647, 10.1002/eji.201545911 · DOI
  119. Hilbert, 2015, Synergistic stimulation with different TLR7 ligands modulates gene expression patterns in the human plasmacytoid dendritic cell Line CAL-1, Mediators Inflamm., 2015, 948540, 10.1155/2015/948540 · DOI
  120. Armitage, 2015, Chlamydia pneumoniae and Chlamydia trachomatis infection differentially modulates human dendritic cell Line (MUTZ) differentiation and activation, Scand. J. Immunol., 82, 48, 10.1111/sji.12295 · DOI · Paper page
  121. Kadengodlu, 2012, Positively charged cholesterol-recombinant human gelatins foster the cellular uptake of proteins and murine immune reactions, Int. J. Nanomed., 7, 5437
  122. Ssemakalu, 2015, The effect of solar irradiated Vibrio cholerae on the secretion of pro-inflammatory cytokines and chemokines by the JAWS II dendritic cell line in vitro, PLoS One, 10, e0130190, 10.1371/journal.pone.0130190 · DOI
  123. Horev-Azaria, 2013, Predictive toxicology of cobalt ferrite nanoparticles: comparative in-vitro study of different cellular models using methods of knowledge discovery from data, Part. Fibre Toxicol., 10, 32, 10.1186/1743-8977-10-32 · DOI
  124. Tomić, 2014, Size-dependent effects of gold nanoparticles uptake on maturation and antitumor functions of human dendritic cells in vitro, PLoS One, 9, e96584, 10.1371/journal.pone.0096584 · DOI
  125. Fernández, 2015, Intracellular accumulation and immunological properties of fluorescent gold nanoclusters in human dendritic cells, Biomaterials, 243, 1, 10.1016/j.biomaterials.2014.11.045 · DOI
  126. Fytianos, 2015, Uptake efficiency of surface modified gold nanoparticles does not correlate with functional changes and cytokine secretion in human dendritic cells in vitro, Nanomedicine, 1, 633, 10.1016/j.nano.2014.11.004 · DOI
  127. Paik, 2015, Characterization quantification, and determination of the toxicity of iron oxide nanoparticles to the bone marrow cells, Int. J. Mol. Sci., 16, 22243, 10.3390/ijms160922243 · DOI
  128. Margaroni, 2016, PLGA nanoparticles modified with a TNFα mimicking peptide, soluble Leishmania antigens and MPLA induce T cell priming in vitro via dendritic cell functional differentiation, Eur. J. Pharm. Biopharm., 105, 18, 10.1016/j.ejpb.2016.05.018 · DOI
  129. Barbosa, 2016, Nanostructured lipid carriers loaded with resveratrol modulate human dendritic cells, Int. J. Nanomed., 11, 3501, 10.2147/IJN.S108694 · DOI
  130. Piazza, 2011, Uniform lipopolysaccharide (LPS)-loaded magnetic nanoparticles for the investigation of LPS-TLR4 signaling, Angew. Chem. Int. Ed. Engl., 50, 622, 10.1002/anie.201004655 · DOI
  131. Nakanishi, 2016, Silica nanoparticles activate purinergic signaling via P2×7 receptor in dendritic cells, leading to production of pro-inflammatory cytokines, Toxicol. In Vitro, 35, 202, 10.1016/j.tiv.2016.06.003 · DOI
  132. Reddy, 2006, Targeting dendritic cells with biomaterials: developing the next generation of vaccines, Trends Immunol., 27, 573, 10.1016/j.it.2006.10.005 · DOI
  133. Manolova, 2008, Nanoparticles target distinct dendritic cell populations according to their size, Eur. J. Immunol., 38, 1404, 10.1002/eji.200737984 · DOI
  134. Demento, 2009, Inflammasome-activating nanoparticles as modular systems for optimizing vaccine efficacy, Vaccine, 27, 3013, 10.1016/j.vaccine.2009.03.034 · DOI · Paper page
  135. Wang, 2016, Self-adjuvanted nanovaccine for cancer immunotherapy: role of lysosomal rupture-induced ROS in MHC class I antigen presentation, Biomaterials, 79, 88, 10.1016/j.biomaterials.2015.11.040 · DOI
  136. Gao, 2017, Cationic liposomes promote antigen cross-presentation in dendritic cells by alkalizing the lysosomal pH and limiting the degradation of antigens, Int. J. Nanomed., 12, 1251, 10.2147/IJN.S125866 · DOI
  137. Seydoux, 2017, Size-dependent accumulation of particles in lysosomes modulates dendritic cell function through impaired antigen degradation, Int. J. Nanomed., 9, 3885
  138. Wibroe, 2014, The role of complement in antibody therapy for infectious diseases, Microbiol. Spectrum, 2, 10.1128/microbiolspec.AID-0015-2014 · DOI
  139. Moghimi, 2014, Cancer nanomedicine and the complement system activation paradigm: anaphylaxis and tumour growth, J. Controlled Release, 190, 556, 10.1016/j.jconrel.2014.03.051 · DOI
  140. Farhangrazi, 2016, Materials etiquette and complement responses, Curr. Bionanotechnol., 2, 6, 10.2174/2213529402666160601125405 · DOI
  141. Moghimi, 2012, Particulate systems for targeting of macrophages: basic and therapeutic concepts, J. Innate Immun., 4, 509, 10.1159/000339153 · DOI
  142. Cornacoff, 1983, Primate erythrocyte-immune complex-bearing mechanism, J. Clin. Invest., 71, 236, 10.1172/JCI110764 · DOI
  143. Loughrey, 1990, The binding of phosphatidylglycerol liposomes to rat platelets is mediated by complement, Thromb. Haemost., 64, 172, 10.1055/s-0038-1647276 · DOI
  144. Moghimi, 2016, Complement propriety and conspiracy in nanomedicine: perspective and a hypothesis, Nucleic Acid Ther., 26, 67, 10.1089/nat.2015.0587 · DOI
  145. Wibroe, 2017, Bypassing adverse injection reactions to nanoparticles through shape modification and attachment to erythrocytes, Nat. Nanotechnol., 12, 589, 10.1038/nnano.2017.47 · DOI
  146. Moghimi, 2014, Just so stories: the random act of anti-cancer nanomedicine performance, Nanomedicine, 10, 1661, 10.1016/j.nano.2014.04.011 · DOI
  147. Guglietta, 2016, hypercoagulation and complement: connected players in tumor development and metastases, Semin. Immunol., 28, 578, 10.1016/j.smim.2016.10.011 · DOI
  148. Hattori, 1989, Complement proteins C5b-9 induce secretion of high molecular-weight multimers of endothelial von Willebrand-factor and translocation of granule membrane-protein GMP-140 to the cell-surface, J. Biol. Chem., 264, 9053, 10.1016/S0021-9258(18)81901-9 · DOI
  149. Moghimi, 2011, Material properties in complement activation, Adv. Drug Deliv. Rev., 63, 1000, 10.1016/j.addr.2011.06.002 · DOI
  150. Hamad, 2010, Distinct polymer architecture mediates switching of complement activation pathways at the nanosphere-serum interface: implications for stealth nanoparticle engineering, ACS Nano, 4, 6629, 10.1021/nn101990a · DOI
  151. Salvador-Morales, 2006, Complement activation and protein adsorption by carbon nanotubes, Mol. Immunol., 43, 193, 10.1016/j.molimm.2005.02.006 · DOI
  152. Pondman, 2014, Complement activation by carbon nanotubes and its influence on the phagocytosis and cytokine response by macrophages, Nanomedicine, 10, 1287, 10.1016/j.nano.2014.02.010 · DOI
  153. Moghimi, 2001, Recognition by macrophages and liver cells of opsonized phospholipid vesicles and phospholipid headgroups, Pharm. Res., 18, 1, 10.1023/A:1011054123304 · DOI
  154. Wang, 2017, In vitro and in vivo differences in murine third complement component (C3) opsonisation and macrophages/leukocyte responses to antibody-functionalized iron oxide nanoworms, Front. Immunol., 8, 151
  155. Feinstein, 1986, Immunoglobulin flexibility in complement activation, Immunol. Today, 7, 169, 10.1016/0167-5699(86)90168-4 · DOI
  156. Strumane, 2014, Complement is activated by Igg hexamers assembled at the cell surface, Science, 343, 1260, 10.1126/science.1248943 · DOI
  157. Feinstein, 1969, Conformation of the free and antigen-bound IgM antibody molecules, Nature, 224, 1307, 10.1038/2241307a0 · DOI
  158. Pedersen, 2010, Curvature of synthetic and natural surfaces is an important target feature in classical pathway complement activation, J. Immunol., 184, 1931, 10.4049/jimmunol.0902214 · DOI
  159. Wibroe, 2016, Soluble and immobilized graphene oxide activates complement system differently dependent on surface oxidation state, Biomaterials, 78, 20, 10.1016/j.biomaterials.2015.11.028 · DOI
  160. Whitehead, 2015, Tumour exosomes display differential mechanical and complement activation properties dependent on malignant state: implications in endothelial leakiness, J. Extracell. Vesicles, 4, 29685, 10.3402/jev.v4.29685 · DOI
  161. Clayton, 2003, Antigen-presenting cell exosomes are protected from complement-mediated lysis by expression of CD55 and CD59, Eur. J. Immunol., 33, 522, 10.1002/immu.200310028 · DOI
  162. Kerr, 2012, Complement-mediated injury and protection of endothelium: lessons from atypical haemolytic uraemic syndrome, Immunobiology, 217, 195, 10.1016/j.imbio.2011.07.028 · DOI
  163. Fujita, 2002, Evolution of the lectin-complement pathway and its role in innate immunity, Nat. Rev. Immunol., 2, 346, 10.1038/nri800 · DOI
  164. Holmskov, 2003, Collections and ficolins: humoral lectins of the innate immune defense, Annu. Rev. Immunol., 21, 547, 10.1146/annurev.immunol.21.120601.140954 · DOI · Paper page
  165. Jensenius, 2009, Mannan-binding lectin: structure, oligomerization, and flexibility studied by atomic force microscopy, J. Mol. Biol., 391, 246, 10.1016/j.jmb.2009.05.083 · DOI
  166. Heja, 2012, Revised mechanism of complement lectin-pathway activation revealing the role of serine protease MASP1 as the exclusive activator of MASP-2, Proc. Natl. Acad. Sci. U. S. A., 109, 10498, 10.1073/pnas.1202588109 · DOI
  167. Hamad, 2008, Complement activation by PEGylated single-walled carbon nanotubes is independent of C1q and alternative pathway turnover, Mol. Immunol., 45, 3797, 10.1016/j.molimm.2008.05.020 · DOI
  168. Andersen, 2013, Single-walled carbon nanotube surface control of complement recognition and activation, ACS Nano, 7, 1108, 10.1021/nn3055175 · DOI
  169. Banda, 2014, Mechanisms of complement activation by dextran-coated superparmagnetic iron oxide (SPIO) nanoworms in mouse versus human serum, Part. Fibre Toxicol., 11, 64, 10.1186/s12989-014-0064-2 · DOI
  170. Inturi, 2015, Modulatory role of surface coating of superparamagnetic iron oxide nanoworms in complement opsonisation and leukocyte uptake, ACS Nano, 9, 10758, 10.1021/acsnano.5b05061 · DOI
  171. Wang, 2016, Activation of human complement system by dextran-coated iron oxide nanoparticles is not affected by dextran/Fe ratio, hydroxyl modifications, and crosslinking, Front. Immunol., 7, 418, 10.3389/fimmu.2016.00418 · DOI
  172. Hamad, 2013, Complement monitoring of Pluronic 127 gel and micelles: suppression of copolymer-mediated complement activation by elevated serum levels of HDL, LDL, and apolipoproteins A1 and B-100, J. Controlled Release, 170, 167, 10.1016/j.jconrel.2013.05.030 · DOI
  173. Matsushita, 1995, Cleavage of the third component of complement (C3) by mannose-binding-protein-associated serine protease (MASP) with subsequent complement activation, Immunobiology, 194, 443, 10.1016/S0171-2985(11)80110-5 · DOI
  174. Dobo, 2016, MASP-3 is the exclusive pro-factor D activator in resting blood: the lectin and the alternative complement pathways are fundamentally linked, Sci. Rep., 6, 31877, 10.1038/srep31877 · DOI
  175. Yu, 2014, Modulation of coplement activation and amplification on nanoparticle surfaces by glycopolymer conformation and chemistry, ACS Nano, 8, 7687, 10.1021/nn504186b · DOI
  176. Wibroe, 2016, An integrated assessment of morphology size, and complement activation of the PEGylated liposomal doxorubicin products Doxil®, Caelyx®, DOXOrubicin, and SinaDoxosome, J. Controlled Release, 221, 1, 10.1016/j.jconrel.2015.11.021 · DOI
  177. Moghimi, 2006, Methylation of the phosphate oxygen moiety of phospholipid-methoxy(polyethylene glycol) conjugate prevents PEGylated liposome-mediated complement activation and anaphylatoxin production, FASEB J., 20, 2591, 10.1096/fj.06-6186fje · DOI
  178. Klapper, 2014, Mediation of a non-proteolytic activation of complement component C3 by phospholipid vesicles, Biomaterials, 35, 3688, 10.1016/j.biomaterials.2013.12.085 · DOI
  179. Chen, 2017, Complement proteins bind to nanoparticle protein corona and undergo dynamic exchange in vivo, Nat. Nanotechnol., 12, 387, 10.1038/nnano.2016.269 · DOI · Paper page
  180. Moghimi, 2003, Stealth liposomes and long circulating nanoparticles: critical issues in pharmacokinetics, opsonisation and protein-binding properties, Prog. Lipid Res., 42, 463, 10.1016/S0163-7827(03)00033-X · DOI
  181. Wibroe, 2015, Citrem modulates internal nanostructure of glyceryl monooleate dispersions and bypasses complement activation: towards development of safe tunable intravenous lipid nanocarriers, Nanomedicine, 11, 1909, 10.1016/j.nano.2015.08.003 · DOI
  182. Azmi, 2016, A structurally diverse library of safe-by-design citrem-phospholipid lamellar and non-lamellar liquid crystalline nano-assemblies, J. Controlled Release, 239, 1, 10.1016/j.jconrel.2016.08.011 · DOI
  183. Sou, 2008, Electrostatic interactions and complement activation on the surface of phospholipid vesicle containing acidic lipids: effect of the structure of acidic groups, Biochim. Biophys. Acta-Biomembr., 1778, 1035, 10.1016/j.bbamem.2008.01.006 · DOI
  184. Mizrahy, 2011, Hyaluronan-coated nanoparticles: the influence of the molecular weight on CD44-hyaluronan interactions and on the immune response, J. Controlled Release, 156, 231, 10.1016/j.jconrel.2011.06.031 · DOI
  185. Moghimi, 2001, Long-circulating and target-specific nanoparticles: theory to practice, Pharmacol. Rev., 53, 283, 10.1016/S0031-6997(24)01494-7 · DOI
  186. Wu, 2011, Protection of nonself surfaces from complement attack by factor H-binding peptides: implications for therapeutic medicine, J. Immunol, 186, 4269, 10.4049/jimmunol.1003802 · DOI
  187. Moghimi, 2017, Complement activation turnover on surfaces of nanoparticles, Nano Today, 10.1016/j.nantod.2017.03.001 · DOI
  188. Wilhelm, 2016, Analysis of nanoparticle delivery to tumours, Nat. Rev. Mater., 1, 16014, 10.1038/natrevmats.2016.14 · DOI · Paper page
  189. Anselmo, 2014, Platelet-like nanoparticles: mimicking shape, flexibility, and surface biology of platelets to target vascular injuries, ACS Nano, 8, 11243, 10.1021/nn503732m · DOI
  190. Key, 2015, Soft discoidal polymeric nanoconstructs resist macrophage uptake and enhance vascular targeting in tumors, ACS Nano, 9, 11628, 10.1021/acsnano.5b04866 · DOI
  191. Kuhn, 2014, Different endocytotic uptake mechanisms for nanoparticles in epithelial cells and macrophages, Beilstein J. Nanotechnol., 5, 1625, 10.3762/bjnano.5.174 · DOI
  192. Boraschi, 2012, Interaction of nanoparticles with immunocompetent cells: nanosafety considerations, Nanomedicine (Lond.), 7, 121, 10.2217/nnm.11.169 · DOI
  193. Oh, 2014, Endocytosis and exocytosis of nanoparticles in mammalian cells, Int. J. Nanomed., 9, 51
  194. Paul, 2013, Phagocytosis dynamics depends on target shape, Biophys. J., 105, 1143, 10.1016/j.bpj.2013.07.036 · DOI
  195. Champion, 2008, Role of particle size in phagocytosis of polymeric microspheres, Pharm. Res., 25, 1815, 10.1007/s11095-008-9562-y · DOI
  196. Decuzzi, 2008, Design maps for nanoparticles targeting the diseased microvasculature, Biomaterials, 29, 377, 10.1016/j.biomaterials.2007.09.025 · DOI
  197. Decuzzi, 2006, The adhesive strength of non-spherical particles mediated by specific interactions, Biomaterials, 27, 5307, 10.1016/j.biomaterials.2006.05.024 · DOI
  198. Lesniak, 2012, Effects of the presence or absence of a protein corona on silica nanoparticle uptake and impact on cells, ACS Nano, 6, 5845, 10.1021/nn300223w · DOI · Paper page
  199. Patra, 2016, Component-specific analysis of plasma protein corona formation on gold nanoparticles using multiplexed surface plasmon resonance, Small, 12, 1174, 10.1002/smll.201501603 · DOI
  200. Sosale, 2015, Macrophage engulfment of a cell or nanoparticle is regulated by unavoidable opsonization a species-specific ‘Marker of Self’CD47, and target physical properties, Curr. Opin. Immunol., 35, 107, 10.1016/j.coi.2015.06.013 · DOI

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Metadata

Authors
Boraschi, D., Italiani, P., Palomba, R., Decuzzi, P., Duschl, A., Fadeel, B., & Moghimi, S. M.
Venue
Seminars in Immunology
Publisher
Elsevier BV
Published
2017-12
Volume
34
Pages
33-51
ISSN
1044-5323
Cited by
310
References
32
Language
en
Funders
  • European Commission (GA 602461, GA 696656)
  • Associazione Italiana per la Ricerca sul Cancro (GA 17664)
  • Horizon 2020 Framework Programme (GA 671881)
  • European Research Council (FP7/2007-2013 / ERC GA 616695)
  • Ministero dell’Istruzione, dell’Università e della Ricerca
  • Stiftelsen för Miljöstrategisk Forskning

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