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Single step isolation and activation of primary CD3 + T lymphocytes using alcohol-dispersed electrospun magnetic nanofibers

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dc.contributor.authorKim, Kwanghee-
dc.contributor.authorAn, Hyo Jin-
dc.contributor.authorJun, Seung-Hyun-
dc.contributor.authorKim, Tae-Jin-
dc.contributor.authorLim, Seon Ah-
dc.contributor.authorPark, Gayoung-
dc.contributor.authorNa, Hyon Bin-
dc.contributor.authorPark, Yong Il-
dc.contributor.authorHyeon, Taeghwan-
dc.contributor.authorYee, Cassian-
dc.contributor.authorBluestone, Jeffrey A.-
dc.contributor.authorKim, Jungbae-
dc.contributor.authorLee, Kyung-Mi-
dc.date.accessioned2020-04-27T13:52:32Z-
dc.date.available2020-04-27T13:52:32Z-
dc.date.created2020-03-17-
dc.date.issued2012-08-
dc.identifier.citationNano Letters, Vol.12 No.8, pp.4018-4024-
dc.identifier.issn1530-6984-
dc.identifier.other92740-
dc.identifier.urihttps://hdl.handle.net/10371/166207-
dc.description.abstractElectrospun polymer nanofibers with entrapped magnetic nanoparticles (magnetic NP-NF) represent a novel scaffold substrate that can be functionalized for single-step isolation and activation of specific lymphocyte subsets. Using a surface-embedded T cell receptor ligand/trigger (anti-CD3 monoclonal antibody), we demonstrate, as proof of principle, the use of magnetic NP-NF to specifically isolate, enrich, and activate CD3(+) T cells from a heterogeneous cell mixture, leading to preferential expansion of CD8(+)CD3(+) T cells. The large surface area, adjustable antibody density, and embedded paramagnetic properties of the NP-NF permitted enhanced activation and expansion; its use represents a strategy that is amenable to an efficient selection process for adoptive cellular therapy as well as for the isolation of other cellular subsets for downstream translational applications.-
dc.language영어-
dc.publisherAmerican Chemical Society-
dc.titleSingle step isolation and activation of primary CD3 + T lymphocytes using alcohol-dispersed electrospun magnetic nanofibers-
dc.typeArticle-
dc.contributor.AlternativeAuthor현택환-
dc.identifier.doi10.1021/nl301388d-
dc.citation.journaltitleNano Letters-
dc.identifier.wosid000307211000024-
dc.identifier.scopusid2-s2.0-84864660595-
dc.citation.endpage4024-
dc.citation.number8-
dc.citation.startpage4018-
dc.citation.volume12-
dc.identifier.sci000307211000024-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorHyeon, Taeghwan-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusCELL THERAPY-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusDURATION-
dc.subject.keywordPlusSCAFFOLD-
dc.subject.keywordPlusVIVO-
dc.subject.keywordAuthorElectrospun magnetic nanofiber-
dc.subject.keywordAuthorCD4(+) T lymphocytes-
dc.subject.keywordAuthorCD8(+) T lymphocytes-
dc.subject.keywordAuthoranti-CD3 monoclonal antibody-
dc.subject.keywordAuthorimmune cell therapy-
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  • College of Engineering
  • School of Chemical and Biological Engineering
Research Area Chemistry, Materials Science

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