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dc.contributor.authorSwee, Lee Kim
dc.contributor.authorTan, Zhen Wei
dc.contributor.authorSanecka, Anna
dc.contributor.authorYoshida, Nagisa
dc.contributor.authorPatel, Harshil
dc.contributor.authorGrotenbreg, Gijsbert
dc.contributor.authorFrickel, Eva-Maria
dc.contributor.authorPloegh, Hidde L
dc.date.accessioned2021-10-27T20:29:02Z
dc.date.available2021-10-27T20:29:02Z
dc.date.issued2016
dc.identifier.urihttps://hdl.handle.net/1721.1/135734
dc.description.abstract<jats:p> T-cell identity is established by the expression of a clonotypic T-cell receptor (TCR), generated by somatic rearrangement of TCRα and β genes. The properties of the TCR determine both the degree of self-reactivity and the repertoire of antigens that can be recognized. For CD8 T cells, the relationship between TCR identity—hence reactivity to self—and effector function(s) remains to be fully understood and has rarely been explored outside of the H-2 <jats:sup>b</jats:sup> haplotype. We measured the affinity of three structurally distinct CD8 T-cell-derived TCRs that recognize the identical H-2 L <jats:sup>d</jats:sup> -restricted epitope, derived from the Rop7 protein of <jats:italic>Toxoplasma gondii</jats:italic> . We used CD8 T cells obtained from mice generated by somatic cell nuclear transfer as the closest approximation of primary T cells with physiological TCR rearrangements and TCR expression levels. First, we demonstrate the common occurrence of secondary rearrangements in endogenously rearranged loci. Furthermore, we characterized and compared the response of Rop7-specific CD8 T-cell clones upon <jats:italic>Toxoplasma gondii</jats:italic> infection as well as effector function and TCR signalling upon antigenic stimulation <jats:italic>in vitro</jats:italic> . Antigen-independent TCR cross-linking <jats:italic>in vitro</jats:italic> uncovered profound intrinsic differences in the effector functions between T-cell clones. Finally, by assessing the degree of self-reactivity and comparing the transcriptomes of naive Rop7 CD8 T cells, we show that lower self-reactivity correlates with lower effector capacity, whereas higher self-reactivity is associated with enhanced effector function as well as cell cycle entry under physiological conditions. Altogether, our data show that potential effector functions and basal proliferation of CD8 T cells are set by self-reactivity thresholds. </jats:p>
dc.language.isoen
dc.publisherThe Royal Society
dc.relation.isversionof10.1098/RSOB.160293
dc.rightsCreative Commons Attribution 4.0 International license
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceOpen Biology
dc.titlePeripheral self-reactivity regulates antigen-specific CD8 T-cell responses and cell division under physiological conditions
dc.typeArticle
dc.identifier.citationSwee, L. K., et al. "Peripheral Self-Reactivity Regulates Antigen-Specific Cd8 T-Cell Responses and Cell Division under Physiological Conditions." Open Biol 6 11 (2016).
dc.relation.journalOpen Biology
dc.eprint.versionFinal published version
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2019-05-14T12:24:07Z
dspace.orderedauthorsSwee, LK; Tan, ZW; Sanecka, A; Yoshida, N; Patel, H; Grotenbreg, G; Frickel, E-M; Ploegh, HL
dspace.date.submission2019-05-14T12:24:08Z
mit.journal.volume6
mit.journal.issue11
mit.metadata.statusAuthority Work and Publication Information Needed


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