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Red blood cell–derived nanoerythrosome for antigen delivery with enhanced cancer immunotherapy
Author(s) -
Xiao Han,
Shufang Shen,
Qin Fan,
Guojun Chen,
Edikan Archibong,
Gianpietro Dotti,
Zhuang Liu,
Zhen Gu,
Chao Wang
Publication year - 2019
Publication title -
science advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.928
H-Index - 146
ISSN - 2375-2548
DOI - 10.1126/sciadv.aaw6870
Subject(s) - antigen , immunotherapy , cancer immunotherapy , cancer research , metastasis , drug delivery , in vivo , cell , red blood cell , medicine , immunology , cancer , immune system , chemistry , biology , biochemistry , microbiology and biotechnology , organic chemistry
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.

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