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Network Representation of T-Cell Repertoire— A Novel Tool to Analyze Immune Response to Cancer Formation
The T cell repertoire potentially presents complexity compatible, or greater than, that of the human brain. T cell based immune response is involved with practically every part of human physiology, and high-throughput biology needed to follow the T-cell repertoire has made great leaps with the adven...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6297828/ https://www.ncbi.nlm.nih.gov/pubmed/30619277 http://dx.doi.org/10.3389/fimmu.2018.02913 |
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author | Priel, Avner Gordin, Miri Philip, Hagit Zilberberg, Alona Efroni, Sol |
author_facet | Priel, Avner Gordin, Miri Philip, Hagit Zilberberg, Alona Efroni, Sol |
author_sort | Priel, Avner |
collection | PubMed |
description | The T cell repertoire potentially presents complexity compatible, or greater than, that of the human brain. T cell based immune response is involved with practically every part of human physiology, and high-throughput biology needed to follow the T-cell repertoire has made great leaps with the advent of massive parallel sequencing [1]. Nevertheless, tools to handle and observe the dynamics of this complexity have only recently started to emerge [e.g., 2, 3, 4] in parallel with sequencing technologies. Here, we present a network-based view of the dynamics of the T cell repertoire, during the course of mammary tumors development in a mouse model. The transition from the T cell receptor as a feature, to network-based clustering, followed by network-based temporal analyses, provides novel insights to the workings of the system and provides novel tools to observe cancer progression via the perspective of the immune system. The crux of the approach here is at the network-motivated clustering. The purpose of the clustering step is not merely data reduction and exposing structures, but rather to detect hubs, or attractors, within the T cell receptor repertoire that might shed light on the behavior of the immune system as a dynamic network. The Clone-Attractor is in fact an extension of the clone concept, i.e., instead of looking at particular clones we observe the extended clonal network by assigning clusters to graph nodes and edges to adjacent clusters (editing distance metric). Viewing the system as dynamical brings to the fore the notion of an attractors landscape, hence the possibility to chart this space and map the sample state at a given time to a vector in this large space. Based on this representation we applied two different methods to demonstrate its effectiveness in identifying changes in the repertoire that correlate with changes in the phenotype: (1) network analysis of the TCR repertoire in which two measures were calculated and demonstrated the ability to differentiate control from transgenic samples, and, (2) machine learning classifier capable of both stratifying control and trangenic samples, as well as to stratify pre-cancer and cancer samples. |
format | Online Article Text |
id | pubmed-6297828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62978282019-01-07 Network Representation of T-Cell Repertoire— A Novel Tool to Analyze Immune Response to Cancer Formation Priel, Avner Gordin, Miri Philip, Hagit Zilberberg, Alona Efroni, Sol Front Immunol Immunology The T cell repertoire potentially presents complexity compatible, or greater than, that of the human brain. T cell based immune response is involved with practically every part of human physiology, and high-throughput biology needed to follow the T-cell repertoire has made great leaps with the advent of massive parallel sequencing [1]. Nevertheless, tools to handle and observe the dynamics of this complexity have only recently started to emerge [e.g., 2, 3, 4] in parallel with sequencing technologies. Here, we present a network-based view of the dynamics of the T cell repertoire, during the course of mammary tumors development in a mouse model. The transition from the T cell receptor as a feature, to network-based clustering, followed by network-based temporal analyses, provides novel insights to the workings of the system and provides novel tools to observe cancer progression via the perspective of the immune system. The crux of the approach here is at the network-motivated clustering. The purpose of the clustering step is not merely data reduction and exposing structures, but rather to detect hubs, or attractors, within the T cell receptor repertoire that might shed light on the behavior of the immune system as a dynamic network. The Clone-Attractor is in fact an extension of the clone concept, i.e., instead of looking at particular clones we observe the extended clonal network by assigning clusters to graph nodes and edges to adjacent clusters (editing distance metric). Viewing the system as dynamical brings to the fore the notion of an attractors landscape, hence the possibility to chart this space and map the sample state at a given time to a vector in this large space. Based on this representation we applied two different methods to demonstrate its effectiveness in identifying changes in the repertoire that correlate with changes in the phenotype: (1) network analysis of the TCR repertoire in which two measures were calculated and demonstrated the ability to differentiate control from transgenic samples, and, (2) machine learning classifier capable of both stratifying control and trangenic samples, as well as to stratify pre-cancer and cancer samples. Frontiers Media S.A. 2018-12-11 /pmc/articles/PMC6297828/ /pubmed/30619277 http://dx.doi.org/10.3389/fimmu.2018.02913 Text en Copyright © 2018 Priel, Gordin, Philip, Zilberberg and Efroni. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Priel, Avner Gordin, Miri Philip, Hagit Zilberberg, Alona Efroni, Sol Network Representation of T-Cell Repertoire— A Novel Tool to Analyze Immune Response to Cancer Formation |
title | Network Representation of T-Cell Repertoire— A Novel Tool to Analyze Immune Response to Cancer Formation |
title_full | Network Representation of T-Cell Repertoire— A Novel Tool to Analyze Immune Response to Cancer Formation |
title_fullStr | Network Representation of T-Cell Repertoire— A Novel Tool to Analyze Immune Response to Cancer Formation |
title_full_unstemmed | Network Representation of T-Cell Repertoire— A Novel Tool to Analyze Immune Response to Cancer Formation |
title_short | Network Representation of T-Cell Repertoire— A Novel Tool to Analyze Immune Response to Cancer Formation |
title_sort | network representation of t-cell repertoire— a novel tool to analyze immune response to cancer formation |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6297828/ https://www.ncbi.nlm.nih.gov/pubmed/30619277 http://dx.doi.org/10.3389/fimmu.2018.02913 |
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