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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
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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. |
format | Online Article Text |
id | pubmed-6535768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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