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dc.contributor.authorXie, Guozhu
dc.contributor.authorDong, Han
dc.contributor.authorLiang, Yong
dc.contributor.authorHam, James Dongjoo
dc.contributor.authorRizwan, Romee
dc.contributor.authorChen, Jianzhu
dc.date.accessioned2022-02-07T15:10:31Z
dc.date.available2021-10-27T20:23:21Z
dc.date.available2022-02-07T15:10:31Z
dc.date.issued2020-09
dc.date.submitted2020-08
dc.identifier.issn2352-3964
dc.identifier.urihttps://hdl.handle.net/1721.1/135407.2
dc.description.abstract© 2020 The Author(s) Natural Killer (NK) cells and CD8+ cytotoxic T cells are two types of immune cells that can kill target cells through similar cytotoxic mechanisms. With the remarkable success of chimeric antigen receptor (CAR)-engineered T (CAR-T) cells for treating haematological malignancies, there is a rapid growing interest in developing CAR-engineered NK (CAR-NK) cells for cancer therapy. Compared to CAR-T cells, CAR-NK cells could offer some significant advantages, including: (1) better safety, such as a lack or minimal cytokine release syndrome and neurotoxicity in autologous setting and graft-versus-host disease in allogenic setting, (2) multiple mechanisms for activating cytotoxic activity, and (3) high feasibility for ‘off-the-shelf’ manufacturing. CAR-NK cells could be engineered to target diverse antigens, enhance proliferation and persistence in vivo, increase infiltration into solid tumours, overcome resistant tumour microenvironment, and ultimately achieve an effective anti-tumour response. In this review, we focus on recent progress in genetic engineering and clinical application of CAR-NK cells, and discuss current challenges and future promise of CAR-NK cells as a novel cellular immunotherapy in cancer.en_US
dc.language.isoen
dc.publisherElsevier BVen_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.ebiom.2020.102975en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourceElsevieren_US
dc.titleCAR-NK cells: A promising cellular immunotherapy for canceren_US
dc.typeArticleen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MIT
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biology
dc.relation.journalEBioMedicineen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2021-07-15T15:35:38Z
dspace.orderedauthorsXie, G; Dong, H; Liang, Y; Ham, JD; Rizwan, R; Chen, Jen_US
dspace.date.submission2021-07-15T15:35:40Z
mit.journal.volume59en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work Neededen_US


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