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Red blood cell-derived nanoerythrosome for antigen delivery with enhanced cancer immunotherapy.

Xiao Han | Shufang Shen | Qin Fan | Guojun Chen | Edikan Archibong | Gianpietro Dotti | Zhuang Liu | Zhen Gu | Chao Wang
Science advances | 2019

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.

Pubmed ID: 31681841

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4T1-Luc [JCRB] (tool)

RRID:CVCL_J239

Cell line 4T1-Luc [JCRB] is a Cancer cell line with a species of origin Mus musculus (Mouse)

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BALB/cAnNCrl (tool)

RRID:MGI:2683685

laboratory mouse with name BALB/cAnNCrl from MGI.

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C57BL/6J (tool)

RRID:IMSR_JAX:000664

Mus musculus with name C57BL/6J from IMSR.

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