Sifting through CD8+ T Cell Memory
In this issue of Immunity, Gerlach et al. (2016) describe three distinct memory CD8+ T cell subsets based upon expression of the fractalkine receptor CX3CR1. Their findings revise the paradigm of effector and central memory T cells by revealing a subset of CD8+ memory T cells defined by intermediate...
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Veröffentlicht in: | Immunity (Cambridge, Mass.) Mass.), 2016-12, Vol.45 (6), p.1184-1186 |
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creator | Martin, Matthew D. Badovinac, Vladimir P. |
description | In this issue of Immunity, Gerlach et al. (2016) describe three distinct memory CD8+ T cell subsets based upon expression of the fractalkine receptor CX3CR1. Their findings revise the paradigm of effector and central memory T cells by revealing a subset of CD8+ memory T cells defined by intermediate levels of expression of CX3CR1 that conducts tissue surveillance.
In this issue of Immunity, Gerlach et al. (2016) describe three distinct memory CD8+ T cell subsets based upon expression of the fractalkine receptor CX3CR1. Their findings revise the paradigm of effector and central memory T cells by revealing a subset of CD8+ memory T cells defined by intermediate levels of expression of CX3CR1 that conducts tissue surveillance. |
doi_str_mv | 10.1016/j.immuni.2016.12.005 |
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In this issue of Immunity, Gerlach et al. (2016) describe three distinct memory CD8+ T cell subsets based upon expression of the fractalkine receptor CX3CR1. Their findings revise the paradigm of effector and central memory T cells by revealing a subset of CD8+ memory T cells defined by intermediate levels of expression of CX3CR1 that conducts tissue surveillance.</description><identifier>ISSN: 1074-7613</identifier><identifier>EISSN: 1097-4180</identifier><identifier>DOI: 10.1016/j.immuni.2016.12.005</identifier><identifier>PMID: 28002725</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>CD8-Positive T-Lymphocytes - immunology ; Cytotoxicity ; Genotype & phenotype ; Immunologic Memory - immunology ; Infections ; Lymphatic system ; Lymphocytes ; Pathogens ; Researchers ; Surveillance ; T cell receptors ; T-Lymphocyte Subsets - immunology</subject><ispartof>Immunity (Cambridge, Mass.), 2016-12, Vol.45 (6), p.1184-1186</ispartof><rights>2016 Elsevier Inc.</rights><rights>Copyright © 2016 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Dec 20, 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c469t-b4095502809af41375436b055c9c0885fbc72080124b2c9f79c11b0ecdda5133</citedby><cites>FETCH-LOGICAL-c469t-b4095502809af41375436b055c9c0885fbc72080124b2c9f79c11b0ecdda5133</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.immuni.2016.12.005$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28002725$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Martin, Matthew D.</creatorcontrib><creatorcontrib>Badovinac, Vladimir P.</creatorcontrib><title>Sifting through CD8+ T Cell Memory</title><title>Immunity (Cambridge, Mass.)</title><addtitle>Immunity</addtitle><description>In this issue of Immunity, Gerlach et al. (2016) describe three distinct memory CD8+ T cell subsets based upon expression of the fractalkine receptor CX3CR1. Their findings revise the paradigm of effector and central memory T cells by revealing a subset of CD8+ memory T cells defined by intermediate levels of expression of CX3CR1 that conducts tissue surveillance.
In this issue of Immunity, Gerlach et al. (2016) describe three distinct memory CD8+ T cell subsets based upon expression of the fractalkine receptor CX3CR1. Their findings revise the paradigm of effector and central memory T cells by revealing a subset of CD8+ memory T cells defined by intermediate levels of expression of CX3CR1 that conducts tissue surveillance.</description><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>Cytotoxicity</subject><subject>Genotype & phenotype</subject><subject>Immunologic Memory - immunology</subject><subject>Infections</subject><subject>Lymphatic system</subject><subject>Lymphocytes</subject><subject>Pathogens</subject><subject>Researchers</subject><subject>Surveillance</subject><subject>T cell receptors</subject><subject>T-Lymphocyte Subsets - immunology</subject><issn>1074-7613</issn><issn>1097-4180</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE1LxDAQhoMorq7-A5GiF0FaZ9KkTS6CrJ-geHDvoU1TzbJt16QV9t-bsurBgwiBSeCZdzIPIUcICQJmF4vENs3Q2oSGV4I0AeBbZA9B5jFDAdvjPWdxnmE6IfveLwCQcQm7ZEIFAM0p3yMnL7bubfsa9W-uG17fotm1OI_m0cwsl9GTaTq3PiA7dbH05vCrTsn89mY-u48fn-8eZlePsWaZ7OOSgeQcQrQsaoZpzlmalcC5lhqE4HWpcwoCkLKSalnnUiOWYHRVFRzTdErONrEr170PxveqsV6HbxSt6QavUHDJRDj_QjGTHIEG9PQXuugG14Y9RopKkVI2BrINpV3nvTO1WjnbFG6tENRoWy3UxrYabSukKtgObcdf4UPZmOqn6VtvAC43gAnePqxxymtrWm0q64zuVdXZvyd8AjPujRc</recordid><startdate>20161220</startdate><enddate>20161220</enddate><creator>Martin, Matthew D.</creator><creator>Badovinac, Vladimir P.</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>6I.</scope><scope>AAFTH</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>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>20161220</creationdate><title>Sifting through CD8+ T Cell Memory</title><author>Martin, Matthew D. ; 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In this issue of Immunity, Gerlach et al. (2016) describe three distinct memory CD8+ T cell subsets based upon expression of the fractalkine receptor CX3CR1. Their findings revise the paradigm of effector and central memory T cells by revealing a subset of CD8+ memory T cells defined by intermediate levels of expression of CX3CR1 that conducts tissue surveillance.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28002725</pmid><doi>10.1016/j.immuni.2016.12.005</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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subjects | CD8-Positive T-Lymphocytes - immunology Cytotoxicity Genotype & phenotype Immunologic Memory - immunology Infections Lymphatic system Lymphocytes Pathogens Researchers Surveillance T cell receptors T-Lymphocyte Subsets - immunology |
title | Sifting through CD8+ T Cell Memory |
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