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Defining the Alloreactive T Cell Repertoire Using High-Throughput Sequencing of Mixed Lymphocyte Reaction Culture

The cellular immune response is the most important mediator of allograft rejection and is a major barrier to transplant tolerance. Delineation of the depth and breadth of the alloreactive T cell repertoire and subsequent application of the technology to the clinic may improve patient outcomes. As a...

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Autores principales: Emerson, Ryan O., Mathew, James M., Konieczna, Iwona M., Robins, Harlan S., Leventhal, Joseph R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4218856/
https://www.ncbi.nlm.nih.gov/pubmed/25365040
http://dx.doi.org/10.1371/journal.pone.0111943
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author Emerson, Ryan O.
Mathew, James M.
Konieczna, Iwona M.
Robins, Harlan S.
Leventhal, Joseph R.
author_facet Emerson, Ryan O.
Mathew, James M.
Konieczna, Iwona M.
Robins, Harlan S.
Leventhal, Joseph R.
author_sort Emerson, Ryan O.
collection PubMed
description The cellular immune response is the most important mediator of allograft rejection and is a major barrier to transplant tolerance. Delineation of the depth and breadth of the alloreactive T cell repertoire and subsequent application of the technology to the clinic may improve patient outcomes. As a first step toward this, we have used MLR and high-throughput sequencing to characterize the alloreactive T cell repertoire in healthy adults at baseline and 3 months later. Our results demonstrate that thousands of T cell clones proliferate in MLR, and that the alloreactive repertoire is dominated by relatively high-abundance T cell clones. This clonal make up is consistently reproducible across replicates and across a span of three months. These results indicate that our technology is sensitive and that the alloreactive TCR repertoire is broad and stable over time. We anticipate that application of this approach to track donor-reactive clones may positively impact clinical management of transplant patients.
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spelling pubmed-42188562014-11-05 Defining the Alloreactive T Cell Repertoire Using High-Throughput Sequencing of Mixed Lymphocyte Reaction Culture Emerson, Ryan O. Mathew, James M. Konieczna, Iwona M. Robins, Harlan S. Leventhal, Joseph R. PLoS One Research Article The cellular immune response is the most important mediator of allograft rejection and is a major barrier to transplant tolerance. Delineation of the depth and breadth of the alloreactive T cell repertoire and subsequent application of the technology to the clinic may improve patient outcomes. As a first step toward this, we have used MLR and high-throughput sequencing to characterize the alloreactive T cell repertoire in healthy adults at baseline and 3 months later. Our results demonstrate that thousands of T cell clones proliferate in MLR, and that the alloreactive repertoire is dominated by relatively high-abundance T cell clones. This clonal make up is consistently reproducible across replicates and across a span of three months. These results indicate that our technology is sensitive and that the alloreactive TCR repertoire is broad and stable over time. We anticipate that application of this approach to track donor-reactive clones may positively impact clinical management of transplant patients. Public Library of Science 2014-11-03 /pmc/articles/PMC4218856/ /pubmed/25365040 http://dx.doi.org/10.1371/journal.pone.0111943 Text en © 2014 Emerson et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Emerson, Ryan O.
Mathew, James M.
Konieczna, Iwona M.
Robins, Harlan S.
Leventhal, Joseph R.
Defining the Alloreactive T Cell Repertoire Using High-Throughput Sequencing of Mixed Lymphocyte Reaction Culture
title Defining the Alloreactive T Cell Repertoire Using High-Throughput Sequencing of Mixed Lymphocyte Reaction Culture
title_full Defining the Alloreactive T Cell Repertoire Using High-Throughput Sequencing of Mixed Lymphocyte Reaction Culture
title_fullStr Defining the Alloreactive T Cell Repertoire Using High-Throughput Sequencing of Mixed Lymphocyte Reaction Culture
title_full_unstemmed Defining the Alloreactive T Cell Repertoire Using High-Throughput Sequencing of Mixed Lymphocyte Reaction Culture
title_short Defining the Alloreactive T Cell Repertoire Using High-Throughput Sequencing of Mixed Lymphocyte Reaction Culture
title_sort defining the alloreactive t cell repertoire using high-throughput sequencing of mixed lymphocyte reaction culture
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4218856/
https://www.ncbi.nlm.nih.gov/pubmed/25365040
http://dx.doi.org/10.1371/journal.pone.0111943
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