Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/92867
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dc.contributorDepartment of Biomedical Engineeringen_US
dc.creatorXiao, Len_US
dc.creatorHuang, Yen_US
dc.creatorYang, Yen_US
dc.creatorMiao, Zen_US
dc.creatorZhu, Jen_US
dc.creatorZhong, Men_US
dc.creatorFeng, Cen_US
dc.creatorTang, Wen_US
dc.creatorZhou, Jen_US
dc.creatorWang, Len_US
dc.creatorZhao, Xen_US
dc.creatorWang, Zen_US
dc.date.accessioned2022-05-26T02:18:07Z-
dc.date.available2022-05-26T02:18:07Z-
dc.identifier.issn2040-3364en_US
dc.identifier.urihttp://hdl.handle.net/10397/92867-
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.rightsThis journal is © The Royal Society of Chemistry 2021en_US
dc.rightsThe following publication Xiao, L., Huang, Y., Yang, Y., Miao, Z., Zhu, J., Zhong, M., ... & Wang, Z. (2021). Biomimetic cytomembrane nanovaccines prevent breast cancer development in the long term. Nanoscale, 13(6), 3594-3601 is available at https://doi.org/10.1039/d0nr08978hen_US
dc.titleBiomimetic cytomembrane nanovaccines prevent breast cancer development in the long termen_US
dc.typeJournal/Magazine Articleen_US
dc.description.otherinformationTitle on author’s file: Biomimetic cytomembrane nanovaccine prevents breast cancer development in the long termen_US
dc.identifier.spage3594en_US
dc.identifier.epage3601en_US
dc.identifier.volume13en_US
dc.identifier.issue6en_US
dc.identifier.doi10.1039/d0nr08978hen_US
dcterms.abstractCytomembrane cancer nanovaccines are considered a promising approach to induce tumor-specific immunity. Most of the currently developed nanovaccines, unfortunately, fail to study the underlying mechanism for cancer prevention and therapy, as well as immune memory establishment, with their long-term anti-tumor immunity remaining unknown. Here, we present a strategy to prepare biomimetic cytomembrane nanovaccines (named CCMP@R837) consisting of antigenic cancer cell membrane (CCM)-capped poly(lactic-co-glycolic acid) (PLGA) nanoparticles loaded with imiquimod (R@837) as an adjuvant to activate the immune system. We found that our CCMP@R837 system enhanced bone-marrow-derived dendritic cell uptake and maturation, as well as increased anti-tumor response against breast cancer 4T1 cells in vitro. Moreover, an immune memory was established after three-time immunization with CCMP@R837 in BALB/c mice. The CCMP@R837-immunized BALB/c mice exhibited suppressed tumor growth and a long survival period (75% of mice lived longer than 50 days after tumor formation). This long-term anti-tumor immunity was achieved by increasing CD8+ T cells and decreasing regulatory T cells in the tumor while increasing effector memory T cells in the spleen. Overall, our platform demonstrates that CCMP@R837 can be a potential candidate for preventive cancer vaccines in the clinic.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationNanoscale, 14 Feb. 2021, v. 13, no. 6, p. 3594-3601en_US
dcterms.isPartOfNanoscaleen_US
dcterms.issued2021-02-14-
dc.identifier.scopus2-s2.0-85101273972-
dc.identifier.pmid33564813-
dc.identifier.eissn2040-3372en_US
dc.description.validate202205 bcfcen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberBME-0041-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextHong Kong Polytecnic University; Hong Kong Research Grants Council; National Natural Science Foundation of China; Natural Science Foundation of Jiangsu Provinceen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS51861700-
dc.description.oaCategoryGreen (AAM)en_US
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