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T cell clonality assessment: past, present and future

T cell clonality testing has important clinical and research value, providing a specific and reproducible assessment of clonal diversity in T cell proliferations. Here we review the conceptual foundations of T cell clonality assays, including T cell ontogeny and T cell receptor structure and functio...

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Autores principales: Mahe, Etienne, Pugh, Tevor, Kamel-Reid, Suzanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868531/
https://www.ncbi.nlm.nih.gov/pubmed/29055897
http://dx.doi.org/10.1136/jclinpath-2017-204761
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author Mahe, Etienne
Pugh, Tevor
Kamel-Reid, Suzanne
author_facet Mahe, Etienne
Pugh, Tevor
Kamel-Reid, Suzanne
author_sort Mahe, Etienne
collection PubMed
description T cell clonality testing has important clinical and research value, providing a specific and reproducible assessment of clonal diversity in T cell proliferations. Here we review the conceptual foundations of T cell clonality assays, including T cell ontogeny and T cell receptor structure and function; we also provide an introduction to T cell receptor genomics and the concept of the T cell clonotype. This is followed by a review of historical and current methods by which T cell clonality may be assayed, including current assay limitations. Some of these assay limitations have been overcome by employing next-generation sequencing (NGS)-based technologies that are becoming a mainstay of modern molecular pathology. In this vein, we provide an introduction to NGS technologies, including a review of the preanalytical, analytical and postanalytical technologies relevant to T cell clonality NGS assays.
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spelling pubmed-58685312018-03-27 T cell clonality assessment: past, present and future Mahe, Etienne Pugh, Tevor Kamel-Reid, Suzanne J Clin Pathol Review T cell clonality testing has important clinical and research value, providing a specific and reproducible assessment of clonal diversity in T cell proliferations. Here we review the conceptual foundations of T cell clonality assays, including T cell ontogeny and T cell receptor structure and function; we also provide an introduction to T cell receptor genomics and the concept of the T cell clonotype. This is followed by a review of historical and current methods by which T cell clonality may be assayed, including current assay limitations. Some of these assay limitations have been overcome by employing next-generation sequencing (NGS)-based technologies that are becoming a mainstay of modern molecular pathology. In this vein, we provide an introduction to NGS technologies, including a review of the preanalytical, analytical and postanalytical technologies relevant to T cell clonality NGS assays. BMJ Publishing Group 2018-03 2017-10-21 /pmc/articles/PMC5868531/ /pubmed/29055897 http://dx.doi.org/10.1136/jclinpath-2017-204761 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Review
Mahe, Etienne
Pugh, Tevor
Kamel-Reid, Suzanne
T cell clonality assessment: past, present and future
title T cell clonality assessment: past, present and future
title_full T cell clonality assessment: past, present and future
title_fullStr T cell clonality assessment: past, present and future
title_full_unstemmed T cell clonality assessment: past, present and future
title_short T cell clonality assessment: past, present and future
title_sort t cell clonality assessment: past, present and future
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868531/
https://www.ncbi.nlm.nih.gov/pubmed/29055897
http://dx.doi.org/10.1136/jclinpath-2017-204761
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