dc.contributor.author | Gerdemann, Ulrike | |
dc.contributor.author | Fleming, Ryan A | |
dc.contributor.author | Kaminski, James | |
dc.contributor.author | McGuckin, Connor | |
dc.contributor.author | Rui, Xianliang | |
dc.contributor.author | Lane, Jennifer F | |
dc.contributor.author | Keskula, Paula | |
dc.contributor.author | Cagnin, Lorenzo | |
dc.contributor.author | Shalek, Alex K | |
dc.contributor.author | Tkachev, Victor | |
dc.contributor.author | Kean, Leslie S | |
dc.date.accessioned | 2022-03-18T14:12:19Z | |
dc.date.available | 2022-03-18T14:12:19Z | |
dc.date.issued | 2021 | |
dc.identifier.uri | https://hdl.handle.net/1721.1/141281 | |
dc.description.abstract | <jats:p>T cell receptor (TCR) clonotype tracking is a powerful tool for interrogating T cell mediated immune processes. New methods to pair a single cell’s transcriptional program with its TCR identity allow monitoring of T cell clonotype-specific transcriptional dynamics. While these technologies have been available for human and mouse T cells studies, they have not been developed for Rhesus Macaques (RM), a critical translational organism for autoimmune diseases, vaccine development and transplantation. We describe a new pipeline, ‘RM-scTCR-Seq’, which, for the first time, enables RM specific single cell TCR amplification, reconstruction and pairing of RM TCR’s with their transcriptional profiles. We apply this method to a RM model of GVHD, and identify and track <jats:italic>in vitro</jats:italic> detected alloreactive clonotypes in GVHD target organs and explore their GVHD driven cytotoxic T cell signature. This novel, state-of-the-art platform fundamentally advances the utility of RM to study protective and pathogenic T cell responses.</jats:p> | en_US |
dc.language.iso | en | |
dc.publisher | Frontiers Media SA | en_US |
dc.relation.isversionof | 10.3389/fimmu.2021.804932 | en_US |
dc.rights | Creative Commons Attribution 4.0 International license | en_US |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | en_US |
dc.source | Frontiers | en_US |
dc.title | Identification and Tracking of Alloreactive T Cell Clones in Rhesus Macaques Through the RM-scTCR-Seq Platform | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Gerdemann, Ulrike, Fleming, Ryan A, Kaminski, James, McGuckin, Connor, Rui, Xianliang et al. 2021. "Identification and Tracking of Alloreactive T Cell Clones in Rhesus Macaques Through the RM-scTCR-Seq Platform." Frontiers in Immunology, 12. | |
dc.contributor.department | Massachusetts Institute of Technology. Department of Chemistry | |
dc.contributor.department | Massachusetts Institute of Technology. Institute for Medical Engineering & Science | |
dc.contributor.department | Koch Institute for Integrative Cancer Research at MIT | |
dc.contributor.department | Ragon Institute of MGH, MIT and Harvard | |
dc.relation.journal | Frontiers in Immunology | en_US |
dc.eprint.version | Final published version | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dc.date.updated | 2022-03-18T14:10:02Z | |
dspace.orderedauthors | Gerdemann, U; Fleming, RA; Kaminski, J; McGuckin, C; Rui, X; Lane, JF; Keskula, P; Cagnin, L; Shalek, AK; Tkachev, V; Kean, LS | en_US |
dspace.date.submission | 2022-03-18T14:10:04Z | |
mit.journal.volume | 12 | en_US |
mit.license | PUBLISHER_CC | |
mit.metadata.status | Authority Work and Publication Information Needed | en_US |