Graphene, other carbon nanomaterials and the immune system: toward nanoimmunity-by-design
Source abstract
Abstract
Abstract Carbon-based materials (CBMs), such as graphene, nanodiamonds, carbon fibers, and carbon dots, have attracted a great deal scientific attention due to their potential as biomedical tools. Following exposure, particularly intravenous injection, these nanomaterials can be recognized by immune cells. Such interactions could be modulated by the different physicochemical properties of the materials (e.g. structure, size, and chemical functions), by either stimulating or suppressing the immune response. However, a harmonized cutting-edge approach for the classification of these materials based not only on their physicochemical parameters but also their immune properties has been missing. The European Commission-funded G-IMMUNOMICS and CARBO-IMmap projects aimed to fill this gap, developing a functional pipeline for the qualitative and quantitative immune characterization of graphene, graphene-related materials (GRMs), and other CBMs. The goal was to open breakthrough perspectives for the definition of the immune profiles of these materials. Here, we summarize our methodological approach, key results, and the necessary multidisciplinary expertise ranging across various fields, from material chemistry to engineering, immunology, toxicology, and systems biology. G-IMMUNOMICS, as a partnering project of the Graphene Flagship, the largest scientific research initiative on graphene worldwide, also complemented the studies performed in the Flagship on health and environmental impact of GRMs. Finally, we present the nanoimmunity-by-design concept, developed within the projects, which can be readily applied to other 2D materials. Overall, the G-IMMUNOMICS and CARBO-IMmap projects have provided new insights on the immune impact of GRMs and CBMs, thus laying the foundation for their safe use and future translation in medicine.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Graphene and Nanomaterials Applications · Carbon and Quantum Dots Applications · Nanoparticles: synthesis and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (100+)
Show source-provided references
1. Electric field effect in atomically thin carbon films10.1126/science.1102896 ↗
2. Graphene gets ready for the big time10.1038/458390a ↗
3. Graphene: status and Prospects10.1126/science.1158877 ↗
4. A roadmap for graphene10.1038/nature11458 ↗
5. Theory of electrical conductivity and dielectric permittivity of highly aligned graphene-based nanocomposites10.1088/1361-648X/aa68ec ↗
6. Production of ready-to-use few-layer graphene in aqueous suspensions10.1038/nprot.2017.142 ↗
7. Classification framework for graphene-based materials10.1002/anie.201403335 ↗
8. Tumor selective uptake of drug-nanodiamond complexes improves therapeutic outcome in pancreatic cancer10.1016/j.nano.2019.02.020 ↗
9. In vivo restoration of myocardial conduction with carbon nanotube fibers10.1161/CIRCEP.119.007256 ↗
10. Preparation, functionalization and characterization of engineered carbon nanodots10.1038/s41596-019-0207-x ↗
11. The graphene times10.1038/s41565-019-0561-4 ↗
12. The application of graphene and its derivatives to energy conversion, storage, and environmental and biosensing devices10.1002/tcr.201500279 ↗
13. Graphene and its derivatives as biomedical materials: future prospects and challenges10.1098/rsfs.2017.0056 ↗
14. Advances on graphene-based nanomaterials for biomedical applications10.1016/j.msec.2018.05.018 ↗
15. The application of graphene-based biomaterials in biomedicine
16. Graphene based materials for biomedical applications10.1016/j.mattod.2013.09.004 ↗
17. Photodynamic therapy based on graphene and MXene in cancer theranostics10.3389/fbioe.2019.00295 ↗
18. Graphene as cancer theranostic tool: progress and future challenges10.7150/thno.11387 ↗
19. Recent advances in carbon based nanosystems for cancer theranostics10.1039/C7BM00008A ↗
20. Rethinking cancer nanotheranostics10.1038/natrevmats.2017.24 ↗
21. Immunological impact of graphene oxide sheets in the abdominal cavity is governed by surface reactivity10.1007/s00204-018-2303-z ↗
22. Safety assessment of graphene-based materials: focus on human health and the environment10.1021/acsnano.8b04758 ↗
23. Graphene and the immune system: challenges and potentiality10.1016/j.addr.2016.05.014 ↗
24. Single-cell mass cytometry and transcriptome profiling reveal the impact of graphene on human immune cells10.1038/s41467-017-01015-3 ↗
25. INSIdE NANO: a systems biology framework to contextualize the mechanism-of-action of engineered nanomaterials10.1038/s41598-018-37411-y ↗
26. Molecular and genomic impact of large and small lateral dimension graphene oxide sheets on human immune cells from healthy donors10.1002/adhm.201500606 ↗
27. A nano-combinatorial library strategy for the discovery of nanotubes with reduced protein-binding, cytotoxicity, and immune response10.1021/nl0730155 ↗
28. Comparative in vivo toxicity, organ biodistribution and immune response of pristine, carboxylated and PEGylated few-layer graphene sheets in Swiss albino mice: A three month study10.1016/j.carbon.2015.08.074 ↗
29. Graphene and the immune system: a romance of many dimensions10.3389/fimmu.2017.00673 ↗
30. Stealth immune properties of graphene oxide enabled by surface-bound complement factor H10.1021/acsnano.6b05409 ↗
31. In vitro evaluation of graphene oxide nanosheets on immune function10.1016/j.jcis.2014.07.004 ↗
32. Graphene oxide attenuates Th2-type immune responses, but augments airway remodeling and hyperresponsiveness in a murine model of asthma10.1021/nn406454u ↗
33. Evidencing the mask effect of graphene oxide: a comparative study on primary human and murine phagocytic cells10.1039/c3nr03543c ↗
34. The role of the lateral dimension of graphene oxide in the regulation of cellular responses10.1016/j.biomaterials.2012.02.021 ↗
35. Crucial role of lateral size for graphene oxide in activating macrophages and stimulating pro-inflammatory responses in cells and animals10.1021/acsnano.5b04751 ↗
36. Cytokine profiling of primary human macrophages exposed to endotoxin-free graphene oxide: size-independent NLRP3 inflammasome activation10.1002/adhm.201700815 ↗
37. Surface Oxidation of Graphene Oxide Determines Membrane Damage, Lipid Peroxidation, and Cytotoxicity in Macrophages in a Pulmonary Toxicity Model10.1021/acsnano.7b07737 ↗
38. Macrophage sensing of single-walled carbon nanotubes via Toll-like receptors10.1038/s41598-018-19521-9 ↗
39. Improved in vitro and in vivo biocompatibility of graphene oxide through surface modification: poly(acrylic acid)-functionalization is superior to PEGylation10.1021/acsnano.6b00539 ↗
40. Impact of carbon nanotubes and graphene on immune cells10.1186/1479-5876-12-138 ↗
41. Designing nanomedicine for immuno-oncology10.1038/s41551-017-0029 ↗
42. Immunity by design10.1016/j.chom.2018.03.017 ↗
43. The cell menagerie: human immune profiling10.1038/525409a ↗
44. Few-layer graphene kills selectively tumor cells from myelomonocytic leukemia patients10.1002/anie.201700078 ↗
45. Towards a classification strategy for complex nanostructures10.1039/C6NH00219F ↗
46. Pulmonary toxicity of carbon nanotubes and asbestos - similarities and differences10.1016/j.addr.2013.07.014 ↗
47. Carbon nanotube translocation to distant organs after pulmonary exposure: insights from in situ 14C-radiolabeling and tissue radioimaging10.1021/nn500475u ↗
48. Lung carcinogenicity of inhaled multi-walled carbon nanotube in rats10.1186/s12989-016-0164-2 ↗
49. Carbon nanotubes added to the SIN List as a nanomaterial of Very High Concern10.1038/s41565-019-0613-9 ↗
50. Pulmonary toxicity of single-wall carbon nanotubes in mice 7 and 90 days after intratracheal instillation10.1093/toxsci/kfg243 ↗
51. Carbon nanotubes introduced into the abdominal cavity of mice show asbestos-like pathogenicity in a pilot study10.1038/nnano.2008.111 ↗
52. Comparative pulmonary toxicity assessment of single-wall carbon nanotubes in rats10.1093/toxsci/kfg228 ↗
53. Exposure to carbon nanotube material: aerosol release during the handling of unrefined single-walled carbon nanotube material10.1080/15287390490253688 ↗
54. Asbestos-like pathogenicity of long carbon nanotubes alleviated by chemical functionalization10.1002/anie.201207664 ↗
55. Toward the suppression of cellular toxicity from single-walled carbon nanotubes10.1039/C5BM00134J ↗
56. Carbon nanotubes exhibit fibrillar pharmacology in primates10.1371/journal.pone.0183902 ↗
57. Structurally uniform and atomically precise carbon nanostructures10.1038/natrevmats.2015.2 ↗
58. Growth of half-meter long carbon nanotubes based on schulz–flory distribution10.1021/nn401995z ↗
59. Banning carbon nanotubes would be scientifically unjustified and damaging to innovation10.1038/s41565-020-0656-y ↗
60. Grouping all carbon nanotubes into a single substance category is scientifically unjustified10.1038/s41565-020-0654-0 ↗
61. The long and short of carbon nanotube toxicity10.1038/nbt0708-774 ↗
62. Emerging systems biology approaches in nanotoxicology: towards a mechanism-based understanding of nanomaterial hazard and risk10.1016/j.taap.2015.12.014 ↗
63. Nanomaterial registry: database that captures the minimal information about nanomaterial physico-chemical characteristics10.1007/s11051-013-2219-8 ↗
64. Properties of nanostructures: data acquisition, categorization, and evaluation10.2481/dsj.010-025 ↗
65. The nanomaterial registry: facilitating the sharing and analysis of data in the diverse nanomaterial community10.2147/IJN.S40722 ↗
66. Immunotoxicity considerations for next generation cancer nanomedicines10.1002/advs.201900133 ↗
67. Biological interactions of carbon-based nanomaterials: from coronation to degradation10.1016/j.nano.2015.11.011 ↗
68. Evaluating the mechanistic evidence and key data gaps in assessing the potential carcinogenicity of carbon nanotubes and nanofibers in humans10.1080/10408444.2016.1206061 ↗
69. Influence of size and shape on the anatomical distribution of endotoxin-free gold nanoparticles10.1021/acsnano.7b00497 ↗
70. Graphene and other 2D materials: a multidisciplinary analysis to uncover the hidden potential as cancer theranostics
71. Bypassing adverse injection reactions to nanoparticles through shape modification and attachment to erythrocytes10.1038/nnano.2017.47 ↗
72. A porcine model of complement-mediated infusion reactions to drug carrier nanosystems and other medicines10.1016/j.addr.2012.07.005 ↗
73. Pseudo-anaphylaxis to polyethylene glycol (PEG)-coated liposomes: roles of anti-PEG IgM and complement activation in a porcine model of human infusion reactions10.1021/acsnano.9b03942 ↗
74. Functionalized multiwalled carbon nanotubes as ultrasound contrast agents10.1073/pnas.1208312109 ↗
75. Conservation and divergence in the transcriptional programs of the human and mouse immune systems10.1073/pnas.1222738110 ↗
76. Immune-cell lineage commitment: translation from mice to humans10.1016/j.immuni.2007.05.011 ↗
77. A prescription for human immunology10.1016/j.immuni.2008.12.003 ↗
78. Tissue-specific transcriptional regulation has diverged significantly between human and mouse10.1038/ng2047 ↗
79. An atlas of combinatorial transcriptional regulation in mouse and man10.1016/j.cell.2010.01.044 ↗
80. Evolution of host innate defence: insights from Caenorhabditis elegans and primitive invertebrates10.1038/nri2689 ↗
81. DNA damage in germ cells induces an innate immune response that triggers systemic stress resistance10.1038/nature12452 ↗
82. DAF-16/FOXO and EGL-27/GATA promote developmental growth in response to persistent somatic DNA damage10.1038/ncb3071 ↗
83. Loss of Caenorhabditis elegans BRCA1 promotes genome stability during replication in smc-5 mutants10.1534/genetics.113.158295 ↗
84. Proliferation tracing with single-cell mass cytometry optimizes generation of stem cell memory-like T cells10.1038/s41587-019-0033-2 ↗
85. The biology of the cell – insights from mass cytometry10.1111/febs.14693 ↗
86. Improved biocompatibility of amino-functionalized graphene oxide in caenorhabditis elegans10.1002/smll.201902699 ↗
87. Stimulation of bone formation by monocyte-activator functionalized graphene oxide in vivo10.1039/C9NR03975A ↗
88. Photocatalytically active graphitic carbon nitride as an effective and safe 2D material for in vitro and in vivo photodynamic therapy10.1002/smll.201904619 ↗
89. Impact of the surface functionalization for nanodiamonds biocompatibility: a comprehensive view on ex vivo human blood immune cell types
90. Poly(ethylene oxide) functionalized graphene nanoribbons with excellent solution processability10.1021/jacs.6b07061 ↗
91. The graphene flagship—a giant european research project10.1002/anie.201504842 ↗
92. Carbon nanotubes degraded by neutrophil myeloperoxidase induce less pulmonary inflammation10.1038/nnano.2010.44 ↗
93. Biodegradation of single-walled carbon nanotubes by eosinophil peroxidase10.1002/smll.201202508 ↗
94. Graphene oxide is degraded by neutrophils and the degradation products are non-genotoxic10.1039/C7NR03552G ↗
95. Degradation of single-layer and few-layer graphene by neutrophil myeloperoxidase10.1002/anie.201806906 ↗
96. Graphene oxide elicits membrane lipid changes and neutrophil extracellular trap formation10.1016/j.chempr.2017.12.017 ↗
97. The perception of nanotechnology and nanomedicine: a worldwide social media study10.2217/nnm.14.78 ↗
98. How can nanotechnology help the fight against breast cancer?10.1039/C8NR02796J ↗
99. A closer look at the genotoxicity of graphene based materials10.1088/2515-7639/ab5844 ↗
100. Advanced tools for the safety assessment of nanomaterials10.1038/s41565-018-0185-0 ↗