Hybrid cellular membrane nanovesicles amplify macrophage immune responses against cancer recurrence and metastasis

The application of STING agonists and the blockade of the SIRPα–CD47 signaling axis are emerging immunotherapeutic strategies. Here the authors show that hybrid cellular membrane nanovesicles loaded with a STING agonist or overexpressing high-affinity SIRPα variants can be exploited to promote anti-...

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Main Authors: Lang Rao, Lei Wu, Zhida Liu, Rui Tian, Guocan Yu, Zijian Zhou, Kuikun Yang, Hong-Gang Xiong, Anli Zhang, Guang-Tao Yu, Wenjing Sun, Han Xu, Jingya Guo, Andrew Li, Hongmin Chen, Zhi-Jun Sun, Yang-Xin Fu, Xiaoyuan Chen
Format: Article
Language:English
Published: Nature Portfolio 2020-09-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-020-18626-y
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author Lang Rao
Lei Wu
Zhida Liu
Rui Tian
Guocan Yu
Zijian Zhou
Kuikun Yang
Hong-Gang Xiong
Anli Zhang
Guang-Tao Yu
Wenjing Sun
Han Xu
Jingya Guo
Andrew Li
Hongmin Chen
Zhi-Jun Sun
Yang-Xin Fu
Xiaoyuan Chen
author_facet Lang Rao
Lei Wu
Zhida Liu
Rui Tian
Guocan Yu
Zijian Zhou
Kuikun Yang
Hong-Gang Xiong
Anli Zhang
Guang-Tao Yu
Wenjing Sun
Han Xu
Jingya Guo
Andrew Li
Hongmin Chen
Zhi-Jun Sun
Yang-Xin Fu
Xiaoyuan Chen
author_sort Lang Rao
collection DOAJ
description The application of STING agonists and the blockade of the SIRPα–CD47 signaling axis are emerging immunotherapeutic strategies. Here the authors show that hybrid cellular membrane nanovesicles loaded with a STING agonist or overexpressing high-affinity SIRPα variants can be exploited to promote anti-tumor immune responses.
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spelling doaj.art-f17de9f800584c86b4d4c951356870bb2022-12-21T22:59:16ZengNature PortfolioNature Communications2041-17232020-09-0111111310.1038/s41467-020-18626-yHybrid cellular membrane nanovesicles amplify macrophage immune responses against cancer recurrence and metastasisLang Rao0Lei Wu1Zhida Liu2Rui Tian3Guocan Yu4Zijian Zhou5Kuikun Yang6Hong-Gang Xiong7Anli Zhang8Guang-Tao Yu9Wenjing Sun10Han Xu11Jingya Guo12Andrew Li13Hongmin Chen14Zhi-Jun Sun15Yang-Xin Fu16Xiaoyuan Chen17Laboratory of Molecular Imaging and Nanomedicine, National Institute of Biomedical Imaging and Bioengineering, National Institutes of HealthState Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST), Key Laboratory of Oral Biomedicine Ministry of Education, School and Hospital of Stomatology, Wuhan UniversityDepartment of Pathology, University of Texas Southwestern Medical CenterLaboratory of Molecular Imaging and Nanomedicine, National Institute of Biomedical Imaging and Bioengineering, National Institutes of HealthLaboratory of Molecular Imaging and Nanomedicine, National Institute of Biomedical Imaging and Bioengineering, National Institutes of HealthLaboratory of Molecular Imaging and Nanomedicine, National Institute of Biomedical Imaging and Bioengineering, National Institutes of HealthLaboratory of Molecular Imaging and Nanomedicine, National Institute of Biomedical Imaging and Bioengineering, National Institutes of HealthState Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST), Key Laboratory of Oral Biomedicine Ministry of Education, School and Hospital of Stomatology, Wuhan UniversityDepartment of Pathology, University of Texas Southwestern Medical CenterState Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST), Key Laboratory of Oral Biomedicine Ministry of Education, School and Hospital of Stomatology, Wuhan UniversityCenter for Molecular Imaging and Translational Medicine, School of Public Health, Xiamen UniversityCenter for Molecular Imaging and Translational Medicine, School of Public Health, Xiamen UniversityChinese Academy of Sciences Key Laboratory of Infection and Immunity, Institute of Biophysics, Chinese Academy of SciencesDepartment of Biomedical Engineering, Johns Hopkins UniversityCenter for Molecular Imaging and Translational Medicine, School of Public Health, Xiamen UniversityState Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST), Key Laboratory of Oral Biomedicine Ministry of Education, School and Hospital of Stomatology, Wuhan UniversityDepartment of Pathology, University of Texas Southwestern Medical CenterLaboratory of Molecular Imaging and Nanomedicine, National Institute of Biomedical Imaging and Bioengineering, National Institutes of HealthThe application of STING agonists and the blockade of the SIRPα–CD47 signaling axis are emerging immunotherapeutic strategies. Here the authors show that hybrid cellular membrane nanovesicles loaded with a STING agonist or overexpressing high-affinity SIRPα variants can be exploited to promote anti-tumor immune responses.https://doi.org/10.1038/s41467-020-18626-y
spellingShingle Lang Rao
Lei Wu
Zhida Liu
Rui Tian
Guocan Yu
Zijian Zhou
Kuikun Yang
Hong-Gang Xiong
Anli Zhang
Guang-Tao Yu
Wenjing Sun
Han Xu
Jingya Guo
Andrew Li
Hongmin Chen
Zhi-Jun Sun
Yang-Xin Fu
Xiaoyuan Chen
Hybrid cellular membrane nanovesicles amplify macrophage immune responses against cancer recurrence and metastasis
Nature Communications
title Hybrid cellular membrane nanovesicles amplify macrophage immune responses against cancer recurrence and metastasis
title_full Hybrid cellular membrane nanovesicles amplify macrophage immune responses against cancer recurrence and metastasis
title_fullStr Hybrid cellular membrane nanovesicles amplify macrophage immune responses against cancer recurrence and metastasis
title_full_unstemmed Hybrid cellular membrane nanovesicles amplify macrophage immune responses against cancer recurrence and metastasis
title_short Hybrid cellular membrane nanovesicles amplify macrophage immune responses against cancer recurrence and metastasis
title_sort hybrid cellular membrane nanovesicles amplify macrophage immune responses against cancer recurrence and metastasis
url https://doi.org/10.1038/s41467-020-18626-y
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