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- W2564775919 abstract "ImmunotherapyVol. 8, No. 11 EditorialNovel T-cell-based vaccines via arming polyclonal CD4+ T cells with antigen-specific exosomesAizhang Xu, Andrew Freywald & Jim XiangAizhang Xu Cancer Research, Saskatchewan Cancer Agency, Saskatoon, Saskatchewan, Canada Department of Oncology, College of Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, CanadaSearch for more papers by this author, Andrew Freywald Department of Pathology, College of Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, CanadaSearch for more papers by this author & Jim Xiang*Author for correspondence: E-mail Address: jim.xiang@usask.ca Cancer Research, Saskatchewan Cancer Agency, Saskatoon, Saskatchewan, Canada Department of Oncology, College of Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, CanadaSearch for more papers by this authorPublished Online:20 Dec 2016https://doi.org/10.2217/imt-2016-0094AboutSectionsView ArticleView Full TextPDF/EPUB ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareShare onFacebookTwitterLinkedInReddit View articleKeywords: exosomesgagpolyclonal T cellsvaccineReferences1 Ramanathan S, Gagnon J, Dubois S, Forand-Boulerice M, Richter MV, Ilangumaran S. 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Nonspecific CD4(+) T cells with uptake of antigen-specific dendritic cell-released exosomes stimulate antigen-specific CD8(+) CTL responses and long-term T cell memory. J. Leukoc. Biol. 82(4), 829–838 (2007).Crossref, Medline, CAS, Google Scholar11 Xie Y, Wang L, Freywald A, Qureshi M, Chen Y, Xiang J. A novel T cell-based vaccine capable of stimulating long-term functional CTL memory against B16 melanoma via CD40L signaling. Cell Mol. Immunol. 10(1), 72–77 (2013).Crossref, Medline, Google Scholar12 Wang R, Xu A, Zhang X et al. Novel exosome-targeted T-cell-based vaccine counteracts T-cell anergy and converts CTL exhaustion in chronic infection via CD40L signaling through the mTORC1 pathway. Cell Mol. Immunol. doi:10.1038/cmi.2016.23 (2016) (Epub ahead of print).Google Scholar13 June CH, Maus MV, Plesa G et al. Engineered T cells for cancer therapy. Cancer Immunol. Immunother. 63(9), 969–975 (2014).Crossref, Medline, CAS, Google Scholar14 Wang L, Xie Y, Ahmed KA et al. 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HIV-1 Gag-specific exosome-targeted T cell-based vaccine stimulates effector CTL responses leading to therapeutic and long-term immunity against Gag/HLA-A2-expressing B16 melanoma in transgenic HLA-A2 mice. Trials Vaccinol. 3, 19–25 (2014).Crossref, Google Scholar18 Vigneron N. Human tumor antigens and cancer immunotherapy. BioMed Res. Int. 2015, 948501 (2015).Crossref, Medline, Google Scholar19 O'neill DW, Adams S, Bhardwaj N. Manipulating dendritic cell biology for the active immunotherapy of cancer. Blood 104(8), 2235–2246 (2004).Crossref, Medline, Google Scholar20 Butler MO, Lee J-S, Ansén S et al. Long-lived antitumor CD8+ lymphocytes for adoptive therapy generated using an artificial antigen-presenting cell. Clin. Cancer Res. 13(6), 1857–1867 (2007).Crossref, Medline, CAS, Google ScholarFiguresReferencesRelatedDetailsCited ByExosome-Based Nanoplatforms: The Emerging Tools for Breast Cancer Therapy28 April 2022 | Frontiers in Oncology, Vol. 12Biological roles and potential applications of immune cell-derived extracellular vesicles22 November 2017 | Journal of Extracellular Vesicles, Vol. 6, No. 1Cancer vaccine clinical trialsSonia Mannan20 December 2016 | Immunotherapy, Vol. 8, No. 11 Vol. 8, No. 11 Follow us on social media for the latest updates Metrics Downloaded 143 times History Published online 20 December 2016 Published in print November 2016 Information© Future Medicine LtdKeywordsexosomesgagpolyclonal T cellsvaccineFinancial & competing interests disclosureThe authors have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties.No writing assistance was utilized in the production of this manuscript.PDF download" @default.
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