dc.contributor.author | Zhang, Ping | |
dc.contributor.author | Lee, Jason S | |
dc.contributor.author | Gartlan, Kate H | |
dc.contributor.author | Schuster, Iona S | |
dc.contributor.author | Comerford, Iain | |
dc.contributor.author | Varelias, Antiopi | |
dc.contributor.author | Ullah, Md Ashik | |
dc.contributor.author | Vuckovic, Slavica | |
dc.contributor.author | Koyama, Motoko | |
dc.contributor.author | Kuns, Rachel D | |
dc.contributor.author | Locke, Kelly R | |
dc.contributor.author | Beckett, Kirrilee J | |
dc.contributor.author | Olver, Stuart D | |
dc.contributor.author | Samson, Luke D | |
dc.contributor.author | et al. | |
dc.date.accessioned | 2021-01-15T04:47:12Z | |
dc.date.available | 2021-01-15T04:47:12Z | |
dc.date.issued | 2017 | |
dc.identifier.issn | 2470-9468 | |
dc.identifier.doi | 10.1126/sciimmunol.aah7152 | |
dc.identifier.uri | http://hdl.handle.net/10072/401156 | |
dc.description.abstract | Type 1 regulatory T (TR1) cells are Foxp3- interleukin-10 (IL-10)-producing CD4+ T cells with potent immunosuppressive properties, but their requirements for lineage development have remained elusive. We show that TR1 cells constitute the most abundant regulatory population after allogeneic bone marrow transplantation (BMT), express the transcription factor Eomesodermin (Eomes), and are critical for the prevention of graft-versus-host disease. We demonstrate that Eomes is required for TR1 cell differentiation, during which it acts in concert with the transcription factor B lymphocyte-induced maturation protein-1 (Blimp-1) by transcriptionally activating IL-10 expression and repressing differentiation into other T helper cell lineages. We further show that Eomes induction in TR1 cells requires T-bet and donor macrophage-derived IL-27. Thus, we define the cellular and transcriptional control of TR1 cell differentiation during BMT, opening new avenues to therapeutic manipulation. | |
dc.description.peerreviewed | Yes | |
dc.language | English | |
dc.publisher | The American Association for the Advancement of Science (AAAS) | |
dc.relation.ispartofpagefrom | eaah7152 | |
dc.relation.ispartofissue | 10 | |
dc.relation.ispartofjournal | Science Immunology | |
dc.relation.ispartofvolume | 2 | |
dc.subject.fieldofresearch | Environmental sciences | |
dc.subject.fieldofresearchcode | 41 | |
dc.subject.keywords | Science & Technology | |
dc.subject.keywords | Life Sciences & Biomedicine | |
dc.subject.keywords | Immunology | |
dc.subject.keywords | VERSUS-HOST-DISEASE | |
dc.subject.keywords | TRANSCRIPTION FACTORS BLIMP-1 | |
dc.title | Eomesodermin promotes the development of type 1 regulatory T (T(R)1) cells | |
dc.type | Journal article | |
dc.type.description | C1 - Articles | |
dcterms.bibliographicCitation | Zhang, P; Lee, JS; Gartlan, KH; Schuster, IS; Comerford, I; Varelias, A; Ullah, MA; Vuckovic, S; Koyama, M; Kuns, RD; Locke, KR; Beckett, KJ; Olver, SD; Samson, LD; et al.; Engwerda, CR; Degli-Esposti, MA; Kallies, A; Tey, S-K; Hill, GR, Eomesodermin promotes the development of type 1 regulatory T (T(R)1) cells, Science Immunology, 2017, 2 (10), pp. eaah7152 | |
dcterms.dateAccepted | 2017-02-22 | |
dc.date.updated | 2021-01-15T04:39:01Z | |
dc.description.version | Accepted Manuscript (AM) | |
gro.rights.copyright | © The Author(s) 2017. This is the author’s version of the work. It is posted here by permission of the AAAS for personal use, not for redistribution. The definitive version was published in Science on 2017, 2 (10), pp. eaah7152, DOI: https://dx.doi.org/10.1126/sciimmunol.aah7152. | |
gro.hasfulltext | Full Text | |
gro.griffith.author | Engwerda, Christian R. | |