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Cytomembrane nanovaccines show therapeutic effects by mimicking tumor cells and antigen presenting cells.


ABSTRACT: Most cancer vaccines are unsuccessful in eliciting clinically relevant effects. Without using exogenous antigens and adoptive cells, we show a concept of utilizing biologically reprogrammed cytomembranes of the fused cells (FCs) derived from dendritic cells (DCs) and cancer cells as tumor vaccines. The fusion of immunologically interrelated two types of cells results in strong expression of the whole tumor antigen complexes and the immunological co-stimulatory molecules on cytomembranes (FMs), allowing the nanoparticle-supported FM (NP@FM) to function like antigen presenting cells (APCs) for T cell immunoactivation. Moreover, tumor-antigen bearing NP@FM can be bio-recognized by DCs to induce DC-mediated T cell immunoactivation. The combination of these two immunoactivation pathways offers powerful antitumor immunoresponse. Through mimicking both APCs and cancer cells, this cytomembrane vaccine strategy can develop various vaccines toward multiple tumor types and provide chances for accommodating diverse functions originating from the supporters.

SUBMITTER: Liu WL 

PROVIDER: S-EPMC6642123 | biostudies-literature | 2019 Jul

REPOSITORIES: biostudies-literature

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Cytomembrane nanovaccines show therapeutic effects by mimicking tumor cells and antigen presenting cells.

Liu Wen-Long WL   Zou Mei-Zhen MZ   Liu Tao T   Zeng Jin-Yue JY   Li Xue X   Yu Wu-Yang WY   Li Chu-Xin CX   Ye Jing-Jie JJ   Song Wen W   Feng Jun J   Zhang Xian-Zheng XZ  

Nature communications 20190719 1


Most cancer vaccines are unsuccessful in eliciting clinically relevant effects. Without using exogenous antigens and adoptive cells, we show a concept of utilizing biologically reprogrammed cytomembranes of the fused cells (FCs) derived from dendritic cells (DCs) and cancer cells as tumor vaccines. The fusion of immunologically interrelated two types of cells results in strong expression of the whole tumor antigen complexes and the immunological co-stimulatory molecules on cytomembranes (FMs), a  ...[more]

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