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Nanomaterials to improve cancer immunotherapy based on ex vivo engineered T cells and NK cells

DC Field Value Language
dc.contributor.authorHan, Bohwa-
dc.contributor.authorSong, Yeonju-
dc.contributor.authorPark, Jeehun-
dc.contributor.authorDoh, Junsang-
dc.date.accessioned2024-05-16T01:21:08Z-
dc.date.available2024-05-16T01:21:08Z-
dc.date.created2022-04-20-
dc.date.created2022-04-20-
dc.date.issued2022-03-
dc.identifier.citationJournal of Controlled Release, Vol.343, pp.379-391-
dc.identifier.issn0168-3659-
dc.identifier.urihttps://hdl.handle.net/10371/202444-
dc.description.abstract© 2022Recent clinical successes of chimeric antigen receptor (CAR) T cell therapy have led the booming of developments in cancer immunotherapy utilizing ex vivo engineered immune cells such as T cells and natural killer (NK) cells. However, a number of issues need to be resolved for this novel therapy to become widely applicable to cancer patients as current CAR-T cell therapies are only successful in treating some blood cancers, and economically not feasible for many patients. In this review, we describe various nanomaterial-based approaches developed to overcome current limitations in ex vivo engineered T/NK cells, along with key biological principles underlying each approach. First, nanomaterials developed to improve ex vivo expansion of T/NK cells and the basic principles of T/NK cell activation for designing nanomaterials are summarized. Second, nanomaterial-based gene delivery methods to generate genetically engineered T/NK cells are discussed with an emphasis on challenges in improving transfection efficacy. Third, nanomaterials loaded to T/NK cells to enhance their anti-tumor functions and to overcome tumor microenvironment are described with key biological characteristics of T/NK cells, which are essential for nanomaterial loading and drug release from the nanomaterials. In particular, we comment on similarities and differences of methods developed for T cells and NK cells based on the biological characteristics of each cell type.-
dc.language영어-
dc.publisherElsevier BV-
dc.titleNanomaterials to improve cancer immunotherapy based on ex vivo engineered T cells and NK cells-
dc.typeArticle-
dc.identifier.doi10.1016/j.jconrel.2022.01.049-
dc.citation.journaltitleJournal of Controlled Release-
dc.identifier.wosid000782077500003-
dc.identifier.scopusid2-s2.0-85124202666-
dc.citation.endpage391-
dc.citation.startpage379-
dc.citation.volume343-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorDoh, Junsang-
dc.type.docTypeReview-
dc.description.journalClass1-
dc.subject.keywordPlusNATURAL-KILLER-CELLS-
dc.subject.keywordPlusANTIGEN-PRESENTING CELLS-
dc.subject.keywordPlusGOLD NANOPARTICLES-
dc.subject.keywordPlusMESSENGER-RNA-
dc.subject.keywordPlusEXPANSION-
dc.subject.keywordPlusDELIVERY-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusIMMUNOMODULATORS-
dc.subject.keywordAuthorCancer immunotherapy-
dc.subject.keywordAuthorNanomaterials-
dc.subject.keywordAuthorNK cells-
dc.subject.keywordAuthorT cells-
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  • College of Engineering
  • Department of Materials Science & Engineering
Research Area Ex Vivo Models, Lymphocyte Biology, Smart Biomaterials

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