Unconventional T Cell Targets for Cancer Immunotherapy
Most studies on the immunotherapeutic potential of T cells have focused on CD8 and CD4 T cells that recognize peptide antigens (Ag) presented by polymorphic major histocompatibility complex (MHC) class I and MHC class II molecules, respectively. However, unconventional T cells, which interact with M...
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Veröffentlicht in: | Immunity (Cambridge, Mass.) Mass.), 2018-03, Vol.48 (3), p.453-473 |
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description | Most studies on the immunotherapeutic potential of T cells have focused on CD8 and CD4 T cells that recognize peptide antigens (Ag) presented by polymorphic major histocompatibility complex (MHC) class I and MHC class II molecules, respectively. However, unconventional T cells, which interact with MHC class Ib and MHC-I like molecules, are also implicated in tumor immunity, although their role therein is unclear. These include unconventional T cells targeting MHC class Ib molecules such as HLA-E and its murine ortholog Qa-1b, natural killer T (NKT) cells, mucosal associated invariant T (MAIT) cells, and γδ T cells. Here, we review the current understanding of the roles of these unconventional T cells in tumor immunity and discuss why further studies into the immunotherapeutic potential of these cells is warranted.
Godfrey et al. review the current understanding of the roles of unconventional T cells in tumor immunity, and discuss the therapeutic potential of harnessing the anti-tumor functions of cells characterized by repeated patterns of TCR usage in unrelated individuals. |
doi_str_mv | 10.1016/j.immuni.2018.03.009 |
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Godfrey et al. review the current understanding of the roles of unconventional T cells in tumor immunity, and discuss the therapeutic potential of harnessing the anti-tumor functions of cells characterized by repeated patterns of TCR usage in unrelated individuals.</description><identifier>ISSN: 1074-7613</identifier><identifier>EISSN: 1097-4180</identifier><identifier>DOI: 10.1016/j.immuni.2018.03.009</identifier><identifier>PMID: 29562195</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Antigens ; Cancer ; Cancer immunotherapy ; CD4 antigen ; CD8 antigen ; Histocompatibility antigen HLA ; Immune system ; Immunity ; Immunotherapy ; Ligands ; Lymphocytes ; Lymphocytes T ; Major histocompatibility complex ; Medical prognosis ; Mucosa ; Mutation ; Natural killer cells ; Peptides ; T cell receptors ; Tumors</subject><ispartof>Immunity (Cambridge, Mass.), 2018-03, Vol.48 (3), p.453-473</ispartof><rights>2018 Elsevier Inc.</rights><rights>Copyright © 2018 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Mar 20, 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c487t-cab571977d7a003b570c68bd03b22a2115ad4bf26ea759af7f5105608af3ebab3</citedby><cites>FETCH-LOGICAL-c487t-cab571977d7a003b570c68bd03b22a2115ad4bf26ea759af7f5105608af3ebab3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1074761318300852$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29562195$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Godfrey, Dale I.</creatorcontrib><creatorcontrib>Le Nours, Jérôme</creatorcontrib><creatorcontrib>Andrews, Daniel M.</creatorcontrib><creatorcontrib>Uldrich, Adam P.</creatorcontrib><creatorcontrib>Rossjohn, Jamie</creatorcontrib><title>Unconventional T Cell Targets for Cancer Immunotherapy</title><title>Immunity (Cambridge, Mass.)</title><addtitle>Immunity</addtitle><description>Most studies on the immunotherapeutic potential of T cells have focused on CD8 and CD4 T cells that recognize peptide antigens (Ag) presented by polymorphic major histocompatibility complex (MHC) class I and MHC class II molecules, respectively. However, unconventional T cells, which interact with MHC class Ib and MHC-I like molecules, are also implicated in tumor immunity, although their role therein is unclear. These include unconventional T cells targeting MHC class Ib molecules such as HLA-E and its murine ortholog Qa-1b, natural killer T (NKT) cells, mucosal associated invariant T (MAIT) cells, and γδ T cells. Here, we review the current understanding of the roles of these unconventional T cells in tumor immunity and discuss why further studies into the immunotherapeutic potential of these cells is warranted.
Godfrey et al. review the current understanding of the roles of unconventional T cells in tumor immunity, and discuss the therapeutic potential of harnessing the anti-tumor functions of cells characterized by repeated patterns of TCR usage in unrelated individuals.</description><subject>Antigens</subject><subject>Cancer</subject><subject>Cancer immunotherapy</subject><subject>CD4 antigen</subject><subject>CD8 antigen</subject><subject>Histocompatibility antigen HLA</subject><subject>Immune system</subject><subject>Immunity</subject><subject>Immunotherapy</subject><subject>Ligands</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Major histocompatibility complex</subject><subject>Medical prognosis</subject><subject>Mucosa</subject><subject>Mutation</subject><subject>Natural killer cells</subject><subject>Peptides</subject><subject>T cell receptors</subject><subject>Tumors</subject><issn>1074-7613</issn><issn>1097-4180</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LxDAQhoMorq7-A5GCFy-tk6ZJ2osgxY-FBS-755CmqWbZNmvSLuy_N6WrBw-eZgLPO5N5ELrBkGDA7GGTmLYdOpOkgPMESAJQnKALDAWPM5zD6djzLOYMkxm69H4DgDNawDmapQVlKS7oBWLrTtlur7ve2E5uo1VU6m0o0n3o3keNdVEpO6VdtBi32f5TO7k7XKGzRm69vj7WOVq_PK_Kt3j5_roon5axynLex0pWlOOC85pLABIeoFhe1aFNU5liTGWdVU3KtOS0kA1vKAbKIJcN0ZWsyBzdT3N3zn4N2veiNV6FH8pO28GLcDsHSgljAb37g27s4MJNEzVyJAtUNlHKWe-dbsTOmVa6g8AgRq9iIyavYyoXQETwGmK3x-FD1er6N_QjMgCPE6CDjb3RTnhldBBXG6dVL2pr_t_wDUWfiYs</recordid><startdate>20180320</startdate><enddate>20180320</enddate><creator>Godfrey, Dale I.</creator><creator>Le Nours, Jérôme</creator><creator>Andrews, Daniel M.</creator><creator>Uldrich, Adam P.</creator><creator>Rossjohn, Jamie</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20180320</creationdate><title>Unconventional T Cell Targets for Cancer Immunotherapy</title><author>Godfrey, Dale I. ; 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subjects | Antigens Cancer Cancer immunotherapy CD4 antigen CD8 antigen Histocompatibility antigen HLA Immune system Immunity Immunotherapy Ligands Lymphocytes Lymphocytes T Major histocompatibility complex Medical prognosis Mucosa Mutation Natural killer cells Peptides T cell receptors Tumors |
title | Unconventional T Cell Targets for Cancer Immunotherapy |
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