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Red blood cell–derived nanoerythrosome for antigen delivery with enhanced cancer immunotherapy
Erythrocytes or red blood cells (RBCs) represent a promising cell-mediated drug delivery platform due to their inherent biocompatibility. Here, we developed an antigen delivery system based on the nanoerythrosomes derived from RBCs, inspired by the splenic antigen-presenting cell targeting capacity...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6810293/ https://www.ncbi.nlm.nih.gov/pubmed/31681841 http://dx.doi.org/10.1126/sciadv.aaw6870 |
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author | Han, Xiao Shen, Shufang Fan, Qin Chen, Guojun Archibong, Edikan Dotti, Gianpietro Liu, Zhuang Gu, Zhen Wang, Chao |
author_facet | Han, Xiao Shen, Shufang Fan, Qin Chen, Guojun Archibong, Edikan Dotti, Gianpietro Liu, Zhuang Gu, Zhen Wang, Chao |
author_sort | Han, Xiao |
collection | PubMed |
description | Erythrocytes or red blood cells (RBCs) represent a promising cell-mediated drug delivery platform due to their inherent biocompatibility. Here, we developed an antigen delivery system based on the nanoerythrosomes derived from RBCs, inspired by the splenic antigen-presenting cell targeting capacity of senescent RBCs. Tumor antigens were loaded onto the nanoerythrosomes by fusing tumor cell membrane–associated antigens with nanoerythrosomes. This tumor antigen–loaded nanoerythrosomes (nano-Ag@erythrosome) elicited antigen responses in vivo and, in combination with the anti–programmed death ligand 1 (PD-L1) blockade, inhibited the tumor growth in B16F10 and 4T1 tumor models. We also generated a tumor model showing that “personalized nano-Ag@erythrosomes” could be achieved by fusing RBCs and surgically removed tumors, which effectively reduced tumor recurrence and metastasis after surgery. |
format | Online Article Text |
id | pubmed-6810293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-68102932019-11-01 Red blood cell–derived nanoerythrosome for antigen delivery with enhanced cancer immunotherapy Han, Xiao Shen, Shufang Fan, Qin Chen, Guojun Archibong, Edikan Dotti, Gianpietro Liu, Zhuang Gu, Zhen Wang, Chao Sci Adv Research Articles Erythrocytes or red blood cells (RBCs) represent a promising cell-mediated drug delivery platform due to their inherent biocompatibility. Here, we developed an antigen delivery system based on the nanoerythrosomes derived from RBCs, inspired by the splenic antigen-presenting cell targeting capacity of senescent RBCs. Tumor antigens were loaded onto the nanoerythrosomes by fusing tumor cell membrane–associated antigens with nanoerythrosomes. This tumor antigen–loaded nanoerythrosomes (nano-Ag@erythrosome) elicited antigen responses in vivo and, in combination with the anti–programmed death ligand 1 (PD-L1) blockade, inhibited the tumor growth in B16F10 and 4T1 tumor models. We also generated a tumor model showing that “personalized nano-Ag@erythrosomes” could be achieved by fusing RBCs and surgically removed tumors, which effectively reduced tumor recurrence and metastasis after surgery. American Association for the Advancement of Science 2019-10-23 /pmc/articles/PMC6810293/ /pubmed/31681841 http://dx.doi.org/10.1126/sciadv.aaw6870 Text en Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Han, Xiao Shen, Shufang Fan, Qin Chen, Guojun Archibong, Edikan Dotti, Gianpietro Liu, Zhuang Gu, Zhen Wang, Chao Red blood cell–derived nanoerythrosome for antigen delivery with enhanced cancer immunotherapy |
title | Red blood cell–derived nanoerythrosome for antigen delivery with enhanced cancer immunotherapy |
title_full | Red blood cell–derived nanoerythrosome for antigen delivery with enhanced cancer immunotherapy |
title_fullStr | Red blood cell–derived nanoerythrosome for antigen delivery with enhanced cancer immunotherapy |
title_full_unstemmed | Red blood cell–derived nanoerythrosome for antigen delivery with enhanced cancer immunotherapy |
title_short | Red blood cell–derived nanoerythrosome for antigen delivery with enhanced cancer immunotherapy |
title_sort | red blood cell–derived nanoerythrosome for antigen delivery with enhanced cancer immunotherapy |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6810293/ https://www.ncbi.nlm.nih.gov/pubmed/31681841 http://dx.doi.org/10.1126/sciadv.aaw6870 |
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