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Engineering Magnetosomes for High-Performance Cancer Vaccination

[Image: see text] A novel cancer vaccine is developed by using Fe(3)O(4) magnetic nanoclusters (MNCs) as the core and cancer cell membranes decorated with anti-CD205 as the cloak. Because of the superparamagnetism and magnetization of MNCs, it is first achieved for the magnetic retention of vaccine...

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Autores principales: Li, Feng, Nie, Weidong, Zhang, Fan, Lu, Guihong, Lv, Chengliang, Lv, Yanlin, Bao, Weier, Zhang, Lijun, Wang, Shuang, Gao, Xiaoyong, Wei, Wei, Xie, Hai-Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6535768/
https://www.ncbi.nlm.nih.gov/pubmed/31139716
http://dx.doi.org/10.1021/acscentsci.9b00060
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author Li, Feng
Nie, Weidong
Zhang, Fan
Lu, Guihong
Lv, Chengliang
Lv, Yanlin
Bao, Weier
Zhang, Lijun
Wang, Shuang
Gao, Xiaoyong
Wei, Wei
Xie, Hai-Yan
author_facet Li, Feng
Nie, Weidong
Zhang, Fan
Lu, Guihong
Lv, Chengliang
Lv, Yanlin
Bao, Weier
Zhang, Lijun
Wang, Shuang
Gao, Xiaoyong
Wei, Wei
Xie, Hai-Yan
author_sort Li, Feng
collection PubMed
description [Image: see text] A novel cancer vaccine is developed by using Fe(3)O(4) magnetic nanoclusters (MNCs) as the core and cancer cell membranes decorated with anti-CD205 as the cloak. Because of the superparamagnetism and magnetization of MNCs, it is first achieved for the magnetic retention of vaccine in the lymph nodes with a magnetic resonance imaging (MRI) guide, which opened the time window for antigen uptake by dendritic cells (DCs). Meanwhile, the camouflaged cancer cell membranes serve as a reservoir of various antigens, enabling subsequent multiantigenic response. Additionally, the decorated anti-CD205 direct more vaccine into CD8(+) DCs, facilitating the major histocompatibility complex (MHC) I cross-presentation. These unique advantages together lead to a great proliferation of T cells with superior clonal diversity and cytotoxic activity. As a result, potent prophylactic and therapeutic effects with few abnormalities are observed on five different tumor models. Therefore, such a cancer-derived magnetosome with the integration of various recent nanotechnologies successfully demonstrates its promise for safe and high-performance cancer vaccination.
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spelling pubmed-65357682019-05-28 Engineering Magnetosomes for High-Performance Cancer Vaccination Li, Feng Nie, Weidong Zhang, Fan Lu, Guihong Lv, Chengliang Lv, Yanlin Bao, Weier Zhang, Lijun Wang, Shuang Gao, Xiaoyong Wei, Wei Xie, Hai-Yan ACS Cent Sci [Image: see text] A novel cancer vaccine is developed by using Fe(3)O(4) magnetic nanoclusters (MNCs) as the core and cancer cell membranes decorated with anti-CD205 as the cloak. Because of the superparamagnetism and magnetization of MNCs, it is first achieved for the magnetic retention of vaccine in the lymph nodes with a magnetic resonance imaging (MRI) guide, which opened the time window for antigen uptake by dendritic cells (DCs). Meanwhile, the camouflaged cancer cell membranes serve as a reservoir of various antigens, enabling subsequent multiantigenic response. Additionally, the decorated anti-CD205 direct more vaccine into CD8(+) DCs, facilitating the major histocompatibility complex (MHC) I cross-presentation. These unique advantages together lead to a great proliferation of T cells with superior clonal diversity and cytotoxic activity. As a result, potent prophylactic and therapeutic effects with few abnormalities are observed on five different tumor models. Therefore, such a cancer-derived magnetosome with the integration of various recent nanotechnologies successfully demonstrates its promise for safe and high-performance cancer vaccination. American Chemical Society 2019-04-03 2019-05-22 /pmc/articles/PMC6535768/ /pubmed/31139716 http://dx.doi.org/10.1021/acscentsci.9b00060 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Li, Feng
Nie, Weidong
Zhang, Fan
Lu, Guihong
Lv, Chengliang
Lv, Yanlin
Bao, Weier
Zhang, Lijun
Wang, Shuang
Gao, Xiaoyong
Wei, Wei
Xie, Hai-Yan
Engineering Magnetosomes for High-Performance Cancer Vaccination
title Engineering Magnetosomes for High-Performance Cancer Vaccination
title_full Engineering Magnetosomes for High-Performance Cancer Vaccination
title_fullStr Engineering Magnetosomes for High-Performance Cancer Vaccination
title_full_unstemmed Engineering Magnetosomes for High-Performance Cancer Vaccination
title_short Engineering Magnetosomes for High-Performance Cancer Vaccination
title_sort engineering magnetosomes for high-performance cancer vaccination
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6535768/
https://www.ncbi.nlm.nih.gov/pubmed/31139716
http://dx.doi.org/10.1021/acscentsci.9b00060
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