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Graphene oxide modulates dendritic cell ability to promote T cell activation and cytokine production
- Source :
- Parker, H, Gravagnuolo, A M, Vranic, S, Crica, L E, Newman, L, Carnell, O, Bussy, C, Dookie, R S, Prestat, E, Haigh, S J, Lozano, N, Kostarelos, K & MacDonald, A S 2022, ' Graphene oxide modulates dendritic cell ability to promote T cell activation and cytokine production ', Nanoscale, vol. 14, no. 46, pp. 17297-17314 . https://doi.org/10.1039/d2nr02169b
- Publication Year :
- 2022
-
Abstract
- An important aspect of immunotherapy is the ability of dendritic cells (DCs) to prime T cell immunity, an approach that has yielded promising results in some early phase clinical trials. However, novel approaches are required to improve DC therapeutic efficacy by enhancing their uptake of, and activation by, disease relevant antigens. The carbon nano-material graphene oxide (GO) may provide a unique way to deliver antigen to innate immune cells and modify their ability to initiate effective adaptive immune responses. We have assessed whether GO of various lateral sizes affects DC activation and function in vitro and in vivo, including their ability to take up, process and present the well-defined model antigen ovalbumin (OVA). We have found that GO flakes are internalised by DCs, while having minimal effect on their viability, activation phenotype or cytokine production. Although adsorption of OVA protein to either small or large GO flakes promoted its uptake into DCs, large GO interfered with OVA processing. In terms of modulation of DC function, delivery of OVA via small GO flakes significantly enhanced DC ability to induce proliferation of OVA-specific CD4 T cells, promoting granzyme B secretion in vitro. On the other hand, delivery of OVA via large GO flakes augmented DC ability to induce proliferation of OVA-specific CD8 T cells, and their production of IFN-γ and granzyme B. Together, these data demonstrate the capacity of GO of different lateral dimensions to act as a promising delivery platform for DC modulation of distinct facets of the adaptive immune response, information that could be exploited for future development of targeted immunotherapies.<br />his work was supported by the Engineering and Physical Sciences Research Council (EPSRC) under the 2D-Health Programme Grant [EP/P00119X/1]. The Nanomedicine Group at ICN2 is partially supported by the CERCA programme, Generalitat de Catalunya, and the Severo Ochoa Centres of Excellence programme, funded by the Spanish Research Agency (AEI, grant no. SEV-2017-0706).
- Subjects :
- Lydia Becker Institute
Ovalbumin
ResearchInstitutes_Networks_Beacons/henry_royce_institute
ResearchInstitutes_Networks_Beacons/03/02
Dendritic Cells
CD8-Positive T-Lymphocytes
Granzymes
Mice, Inbred C57BL
Mice
National Graphene Institute
ResearchInstitutes_Networks_Beacons/lydia_becker_institute_of_immunology_and_inflammation
ResearchInstitutes_Networks_Beacons/national_graphene_institute
Henry Royce Institute
Animals
Cytokines
General Materials Science
Antigens
Advanced materials
Subjects
Details
- ISSN :
- 20403372
- Volume :
- 14
- Issue :
- 46
- Database :
- OpenAIRE
- Journal :
- Nanoscale
- Accession number :
- edsair.doi.dedup.....47eabdaa2e9cf8348085741dfc8754a3
- Full Text :
- https://doi.org/10.1039/d2nr02169b