Overview of methodologies for T-cell receptor repertoire analysis
Abstract Background The T-cell receptor (TCR), located on the surface of T cells, is responsible for the recognition of the antigen-major histocompatibility complex, leading to the initiation of an inflammatory response. Analysing the TCR repertoire may help to gain a better understanding of the imm...
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doaj-98b1f484eb674b13b1c65cf71798ae7c2020-11-25T03:56:49ZengBMCBMC Biotechnology1472-67502017-07-0117111610.1186/s12896-017-0379-9Overview of methodologies for T-cell receptor repertoire analysisElisa Rosati0C Marie Dowds1Evaggelia Liaskou2Eva Kristine Klemsdal Henriksen3Tom H Karlsen4Andre Franke5Institute of Clinical Molecular Biology, Kiel UniversityInstitute of Clinical Molecular Biology, Kiel UniversityCentre for Liver Research and NIHR Birmingham Liver Biomedical Research Unit, Institute of Immunology and Immunotherapy, University of BirminghamNorwegian PSC Research Center, Department of Transplantation Medicine, Division of Surgery, Inflammatory Medicine and Transplantation, Oslo University Hospital RikshospitaletNorwegian PSC Research Center, Department of Transplantation Medicine, Division of Surgery, Inflammatory Medicine and Transplantation, Oslo University Hospital RikshospitaletInstitute of Clinical Molecular Biology, Kiel UniversityAbstract Background The T-cell receptor (TCR), located on the surface of T cells, is responsible for the recognition of the antigen-major histocompatibility complex, leading to the initiation of an inflammatory response. Analysing the TCR repertoire may help to gain a better understanding of the immune system features and of the aetiology and progression of diseases, in particular those with unknown antigenic triggers. The extreme diversity of the TCR repertoire represents a major analytical challenge; this has led to the development of specialized methods which aim to characterize the TCR repertoire in-depth. Currently, next generation sequencing based technologies are most widely employed for the high-throughput analysis of the immune cell repertoire. Results Here, we report on the latest methodological advancements in the field by describing and comparing the available tools; from the choice of the starting material and library preparation method, to the sequencing technologies and data analysis. Finally, we provide a practical example and our own experience by reporting some exemplary results from a small internal benchmark study, where current approaches from the literature and the market are employed and compared. Conclusions Several valid methods for clonotype identification and TCR repertoire analysis exist, however, a gold standard method for the field has not yet been identified. Depending on the purpose of the scientific study, some approaches may be more suitable than others. Finally, due to possible method specific biases, scientists must be careful when comparing results obtained using different methods.http://link.springer.com/article/10.1186/s12896-017-0379-9T-cell receptor (TCR)TCR profilingTCR repertoireImmune repertoireImmunogeneticsImmunogenomics |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Elisa Rosati C Marie Dowds Evaggelia Liaskou Eva Kristine Klemsdal Henriksen Tom H Karlsen Andre Franke |
spellingShingle |
Elisa Rosati C Marie Dowds Evaggelia Liaskou Eva Kristine Klemsdal Henriksen Tom H Karlsen Andre Franke Overview of methodologies for T-cell receptor repertoire analysis BMC Biotechnology T-cell receptor (TCR) TCR profiling TCR repertoire Immune repertoire Immunogenetics Immunogenomics |
author_facet |
Elisa Rosati C Marie Dowds Evaggelia Liaskou Eva Kristine Klemsdal Henriksen Tom H Karlsen Andre Franke |
author_sort |
Elisa Rosati |
title |
Overview of methodologies for T-cell receptor repertoire analysis |
title_short |
Overview of methodologies for T-cell receptor repertoire analysis |
title_full |
Overview of methodologies for T-cell receptor repertoire analysis |
title_fullStr |
Overview of methodologies for T-cell receptor repertoire analysis |
title_full_unstemmed |
Overview of methodologies for T-cell receptor repertoire analysis |
title_sort |
overview of methodologies for t-cell receptor repertoire analysis |
publisher |
BMC |
series |
BMC Biotechnology |
issn |
1472-6750 |
publishDate |
2017-07-01 |
description |
Abstract Background The T-cell receptor (TCR), located on the surface of T cells, is responsible for the recognition of the antigen-major histocompatibility complex, leading to the initiation of an inflammatory response. Analysing the TCR repertoire may help to gain a better understanding of the immune system features and of the aetiology and progression of diseases, in particular those with unknown antigenic triggers. The extreme diversity of the TCR repertoire represents a major analytical challenge; this has led to the development of specialized methods which aim to characterize the TCR repertoire in-depth. Currently, next generation sequencing based technologies are most widely employed for the high-throughput analysis of the immune cell repertoire. Results Here, we report on the latest methodological advancements in the field by describing and comparing the available tools; from the choice of the starting material and library preparation method, to the sequencing technologies and data analysis. Finally, we provide a practical example and our own experience by reporting some exemplary results from a small internal benchmark study, where current approaches from the literature and the market are employed and compared. Conclusions Several valid methods for clonotype identification and TCR repertoire analysis exist, however, a gold standard method for the field has not yet been identified. Depending on the purpose of the scientific study, some approaches may be more suitable than others. Finally, due to possible method specific biases, scientists must be careful when comparing results obtained using different methods. |
topic |
T-cell receptor (TCR) TCR profiling TCR repertoire Immune repertoire Immunogenetics Immunogenomics |
url |
http://link.springer.com/article/10.1186/s12896-017-0379-9 |
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