TCR repertoires of intratumoral T-cell subsets
Summary The infiltration of human tumors by T cells is a common phenomenon, and over the past decades, it has become increasingly clear that the nature of such intratumoral T‐cell populations can predict disease course. Furthermore, intratumoral T cells have been utilized therapeutically in clinical...
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Veröffentlicht in: | Immunological reviews 2014-01, Vol.257 (1), p.72-82 |
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creator | Linnemann, Carsten Mezzadra, Riccardo Schumacher, Ton N. M. |
description | Summary
The infiltration of human tumors by T cells is a common phenomenon, and over the past decades, it has become increasingly clear that the nature of such intratumoral T‐cell populations can predict disease course. Furthermore, intratumoral T cells have been utilized therapeutically in clinical studies of adoptive T‐cell therapy. In this review, we describe how novel methods that are either based on T‐cell receptor (TCR) sequencing or on cancer exome analysis allow the analysis of the tumor reactivity and antigen‐specificity of the intratumoral TCR repertoire with unprecedented detail. Furthermore, we discuss studies that have started to utilize these techniques to probe the link between cancer exomes and the intratumoral TCR pool. Based on the observation that both the cancer epitope repertoire and intratumoral TCR repertoire appear highly individual, we outline strategies, such as ‘autologous TCR gene therapy’, that exploit the tumor‐resident TCR repertoire for the development of personalized immunotherapy. |
doi_str_mv | 10.1111/imr.12140 |
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The infiltration of human tumors by T cells is a common phenomenon, and over the past decades, it has become increasingly clear that the nature of such intratumoral T‐cell populations can predict disease course. Furthermore, intratumoral T cells have been utilized therapeutically in clinical studies of adoptive T‐cell therapy. In this review, we describe how novel methods that are either based on T‐cell receptor (TCR) sequencing or on cancer exome analysis allow the analysis of the tumor reactivity and antigen‐specificity of the intratumoral TCR repertoire with unprecedented detail. Furthermore, we discuss studies that have started to utilize these techniques to probe the link between cancer exomes and the intratumoral TCR pool. Based on the observation that both the cancer epitope repertoire and intratumoral TCR repertoire appear highly individual, we outline strategies, such as ‘autologous TCR gene therapy’, that exploit the tumor‐resident TCR repertoire for the development of personalized immunotherapy.</description><identifier>ISSN: 0105-2896</identifier><identifier>EISSN: 1600-065X</identifier><identifier>DOI: 10.1111/imr.12140</identifier><identifier>PMID: 24329790</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Animals ; Antigens, Neoplasm - immunology ; cancer exome ; gene therapy ; Genetic Therapy ; Humans ; Immunotherapy ; Lymphocytes, Tumor-Infiltrating - immunology ; Lymphocytes, Tumor-Infiltrating - metabolism ; MHC-multimer ; Neoplasms - genetics ; Neoplasms - immunology ; Neoplasms - therapy ; Receptors, Antigen, T-Cell - genetics ; Receptors, Antigen, T-Cell - metabolism ; T cell ; T-Lymphocyte Subsets - immunology ; T-Lymphocyte Subsets - metabolism ; TCR</subject><ispartof>Immunological reviews, 2014-01, Vol.257 (1), p.72-82</ispartof><rights>2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3960-7975d41c9220583125a9b5e80822cb0a2a2258566b3f1d0c665e6133ad887ebf3</citedby><cites>FETCH-LOGICAL-c3960-7975d41c9220583125a9b5e80822cb0a2a2258566b3f1d0c665e6133ad887ebf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fimr.12140$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fimr.12140$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24329790$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Linnemann, Carsten</creatorcontrib><creatorcontrib>Mezzadra, Riccardo</creatorcontrib><creatorcontrib>Schumacher, Ton N. M.</creatorcontrib><title>TCR repertoires of intratumoral T-cell subsets</title><title>Immunological reviews</title><addtitle>Immunol Rev</addtitle><description>Summary
The infiltration of human tumors by T cells is a common phenomenon, and over the past decades, it has become increasingly clear that the nature of such intratumoral T‐cell populations can predict disease course. Furthermore, intratumoral T cells have been utilized therapeutically in clinical studies of adoptive T‐cell therapy. In this review, we describe how novel methods that are either based on T‐cell receptor (TCR) sequencing or on cancer exome analysis allow the analysis of the tumor reactivity and antigen‐specificity of the intratumoral TCR repertoire with unprecedented detail. Furthermore, we discuss studies that have started to utilize these techniques to probe the link between cancer exomes and the intratumoral TCR pool. Based on the observation that both the cancer epitope repertoire and intratumoral TCR repertoire appear highly individual, we outline strategies, such as ‘autologous TCR gene therapy’, that exploit the tumor‐resident TCR repertoire for the development of personalized immunotherapy.</description><subject>Animals</subject><subject>Antigens, Neoplasm - immunology</subject><subject>cancer exome</subject><subject>gene therapy</subject><subject>Genetic Therapy</subject><subject>Humans</subject><subject>Immunotherapy</subject><subject>Lymphocytes, Tumor-Infiltrating - immunology</subject><subject>Lymphocytes, Tumor-Infiltrating - metabolism</subject><subject>MHC-multimer</subject><subject>Neoplasms - genetics</subject><subject>Neoplasms - immunology</subject><subject>Neoplasms - therapy</subject><subject>Receptors, Antigen, T-Cell - genetics</subject><subject>Receptors, Antigen, T-Cell - metabolism</subject><subject>T cell</subject><subject>T-Lymphocyte Subsets - immunology</subject><subject>T-Lymphocyte Subsets - metabolism</subject><subject>TCR</subject><issn>0105-2896</issn><issn>1600-065X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkLFOwzAQhi0EoqUw8AIoIwxpz3ZsxyOqSikKIJWisllO4kiBpCl2Iujbk5K2GxK33PL9_50-hC4xDHE7o7y0Q0xwAEeojzmAD5y9HaM-YGA-CSXvoTPn3gGwoCQ4RT0SUCKFhD4aLsZzz5q1sXWVW-O8KvPyVW113ZSV1YW38BNTFJ5rYmdqd45OMl04c7HbA_R6N1mM7_3oeTob30Z-QiUHX0jB0gAnkhBgIcWEaRkzE0JISBKDJpoQFjLOY5rhFBLOmeGYUp2GoTBxRgfouutd2-qzMa5WZe62j-iVqRqncCAJB9be-gcqBOOstdOiNx2a2Mo5azK1tnmp7UZhUFuTqjWpfk227NWutolLkx7IvboWGHXAV16Yzd9NavY431f6XSJ3tfk-JLT9UFxQwdTyaaoeoojNly9YYfoDQ9-JFA</recordid><startdate>201401</startdate><enddate>201401</enddate><creator>Linnemann, Carsten</creator><creator>Mezzadra, Riccardo</creator><creator>Schumacher, Ton N. M.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7T5</scope><scope>H94</scope></search><sort><creationdate>201401</creationdate><title>TCR repertoires of intratumoral T-cell subsets</title><author>Linnemann, Carsten ; Mezzadra, Riccardo ; Schumacher, Ton N. M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3960-7975d41c9220583125a9b5e80822cb0a2a2258566b3f1d0c665e6133ad887ebf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Antigens, Neoplasm - immunology</topic><topic>cancer exome</topic><topic>gene therapy</topic><topic>Genetic Therapy</topic><topic>Humans</topic><topic>Immunotherapy</topic><topic>Lymphocytes, Tumor-Infiltrating - immunology</topic><topic>Lymphocytes, Tumor-Infiltrating - metabolism</topic><topic>MHC-multimer</topic><topic>Neoplasms - genetics</topic><topic>Neoplasms - immunology</topic><topic>Neoplasms - therapy</topic><topic>Receptors, Antigen, T-Cell - genetics</topic><topic>Receptors, Antigen, T-Cell - metabolism</topic><topic>T cell</topic><topic>T-Lymphocyte Subsets - immunology</topic><topic>T-Lymphocyte Subsets - metabolism</topic><topic>TCR</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Linnemann, Carsten</creatorcontrib><creatorcontrib>Mezzadra, Riccardo</creatorcontrib><creatorcontrib>Schumacher, Ton N. M.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Immunological reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Linnemann, Carsten</au><au>Mezzadra, Riccardo</au><au>Schumacher, Ton N. M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>TCR repertoires of intratumoral T-cell subsets</atitle><jtitle>Immunological reviews</jtitle><addtitle>Immunol Rev</addtitle><date>2014-01</date><risdate>2014</risdate><volume>257</volume><issue>1</issue><spage>72</spage><epage>82</epage><pages>72-82</pages><issn>0105-2896</issn><eissn>1600-065X</eissn><abstract>Summary
The infiltration of human tumors by T cells is a common phenomenon, and over the past decades, it has become increasingly clear that the nature of such intratumoral T‐cell populations can predict disease course. Furthermore, intratumoral T cells have been utilized therapeutically in clinical studies of adoptive T‐cell therapy. In this review, we describe how novel methods that are either based on T‐cell receptor (TCR) sequencing or on cancer exome analysis allow the analysis of the tumor reactivity and antigen‐specificity of the intratumoral TCR repertoire with unprecedented detail. Furthermore, we discuss studies that have started to utilize these techniques to probe the link between cancer exomes and the intratumoral TCR pool. Based on the observation that both the cancer epitope repertoire and intratumoral TCR repertoire appear highly individual, we outline strategies, such as ‘autologous TCR gene therapy’, that exploit the tumor‐resident TCR repertoire for the development of personalized immunotherapy.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>24329790</pmid><doi>10.1111/imr.12140</doi><tpages>11</tpages></addata></record> |
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subjects | Animals Antigens, Neoplasm - immunology cancer exome gene therapy Genetic Therapy Humans Immunotherapy Lymphocytes, Tumor-Infiltrating - immunology Lymphocytes, Tumor-Infiltrating - metabolism MHC-multimer Neoplasms - genetics Neoplasms - immunology Neoplasms - therapy Receptors, Antigen, T-Cell - genetics Receptors, Antigen, T-Cell - metabolism T cell T-Lymphocyte Subsets - immunology T-Lymphocyte Subsets - metabolism TCR |
title | TCR repertoires of intratumoral T-cell subsets |
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