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dc.contributor.authorYong, Kylie Su Mei
dc.contributor.authorHer, Zhisheng
dc.contributor.authorTan, Sue Yee
dc.contributor.authorTan, Wilson Wei Sheng
dc.contributor.authorLiu, Min
dc.contributor.authorLai, Fritz
dc.contributor.authorHeng, Shi Min
dc.contributor.authorFan, Yong
dc.contributor.authorChang, Kenneth Tou En
dc.contributor.authorWang, Cheng-I
dc.contributor.authorChan, Jerry Kok Yen
dc.contributor.authorChen, Jianzhu
dc.contributor.authorChen, Qingfeng
dc.date.accessioned2022-03-14T17:35:57Z
dc.date.available2021-10-27T19:58:20Z
dc.date.available2022-03-14T17:35:57Z
dc.date.issued2020-10
dc.date.submitted2020-04
dc.identifier.issn1664-3224
dc.identifier.urihttps://hdl.handle.net/1721.1/134146.2
dc.description.abstract© Copyright © 2020 Yong, Her, Tan, Tan, Liu, Lai, Heng, Fan, Chang, Wang, Chan, Chen and Chen. Advancements in science enable researchers to constantly innovate and create novel biologics. However, the use of non-human animal models during the development of biologics impedes identification of precise in vivo interactions between the human immune system and treatments. Due to lack of this understanding, adverse effects are frequently observed in healthy volunteers and patients exposed to potential biologics during clinical trials. In this study, we evaluated and compared the effects of known immunotoxic biologics, Proleukin®/IL-2 and OKT3 in humanized mice (reconstituted with human fetal cells) to published clinical outcomes. We demonstrated that humanized mice were able to recapitulate in vivo pathological changes and human-specific immune responses, such as elevated cytokine levels and modulated lymphocytes and myeloid subsets. Given the high similarities of immunological side effects observed between humanized mice and clinical studies, this model could be used to assess immunotoxicity of biologics at a pre-clinical stage, without placing research participants and/or patients at risk.en_US
dc.language.isoen
dc.publisherFrontiers Media SAen_US
dc.relation.isversionofhttp://dx.doi.org/10.3389/fimmu.2020.553362en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceFrontiersen_US
dc.titleHumanized Mouse as a Tool to Predict Immunotoxicity of Human Biologicsen_US
dc.typeArticleen_US
dc.contributor.departmentSingapore-MIT Alliance in Research and Technology (SMART)
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MIT
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biology
dc.relation.journalFrontiers in Immunologyen_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.updated2021-07-15T15:53:13Z
dspace.orderedauthorsYong, KSM; Her, Z; Tan, SY; Tan, WWS; Liu, M; Lai, F; Heng, SM; Fan, Y; Chang, KTE; Wang, C-I; Chan, JKY; Chen, J; Chen, Qen_US
dspace.date.submission2021-07-15T15:53:15Z
mit.journal.volume11en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work Neededen_US


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