Memory-like HCV-specific CD8+ T cells retain a molecular scar after cure of chronic HCV infection
In chronic hepatitis C virus (HCV) infection, exhausted HCV-specific CD8 + T cells comprise memory-like and terminally exhausted subsets. However, little is known about the molecular profile and fate of these two subsets after the elimination of chronic antigen stimulation by direct-acting antiviral...
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Veröffentlicht in: | Nature immunology 2021-02, Vol.22 (2), p.229-239 |
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creator | Hensel, Nina Gu, Zuguang Sagar Wieland, Dominik Jechow, Katharina Kemming, Janine Llewellyn-Lacey, Sian Gostick, Emma Sogukpinar, Oezlem Emmerich, Florian Price, David A. Bengsch, Bertram Boettler, Tobias Neumann-Haefelin, Christoph Eils, Roland Conrad, Christian Bartenschlager, Ralf Grün, Dominic Ishaque, Naveed Thimme, Robert Hofmann, Maike |
description | In chronic hepatitis C virus (HCV) infection, exhausted HCV-specific CD8
+
T cells comprise memory-like and terminally exhausted subsets. However, little is known about the molecular profile and fate of these two subsets after the elimination of chronic antigen stimulation by direct-acting antiviral (DAA) therapy. Here, we report a progenitor–progeny relationship between memory-like and terminally exhausted HCV-specific CD8
+
T cells via an intermediate subset. Single-cell transcriptomics implicated that memory-like cells are maintained and terminally exhausted cells are lost after DAA-mediated cure, resulting in a memory polarization of the overall HCV-specific CD8
+
T cell response. However, an exhausted core signature of memory-like CD8
+
T cells was still detectable, including, to a smaller extent, in HCV-specific CD8
+
T cells targeting variant epitopes. These results identify a molecular signature of T cell exhaustion that is maintained as a chronic scar in HCV-specific CD8
+
T cells even after the cessation of chronic antigen stimulation.
Thimme and colleagues identify a molecular signature of T cell exhaustion resembling a ‘chronic scar’ that is imprinted in hepatitis C virus–specific CD8
+
T cells and cannot simply be reversed by viral clearance. |
doi_str_mv | 10.1038/s41590-020-00817-w |
format | Article |
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+
T cells comprise memory-like and terminally exhausted subsets. However, little is known about the molecular profile and fate of these two subsets after the elimination of chronic antigen stimulation by direct-acting antiviral (DAA) therapy. Here, we report a progenitor–progeny relationship between memory-like and terminally exhausted HCV-specific CD8
+
T cells via an intermediate subset. Single-cell transcriptomics implicated that memory-like cells are maintained and terminally exhausted cells are lost after DAA-mediated cure, resulting in a memory polarization of the overall HCV-specific CD8
+
T cell response. However, an exhausted core signature of memory-like CD8
+
T cells was still detectable, including, to a smaller extent, in HCV-specific CD8
+
T cells targeting variant epitopes. These results identify a molecular signature of T cell exhaustion that is maintained as a chronic scar in HCV-specific CD8
+
T cells even after the cessation of chronic antigen stimulation.
Thimme and colleagues identify a molecular signature of T cell exhaustion resembling a ‘chronic scar’ that is imprinted in hepatitis C virus–specific CD8
+
T cells and cannot simply be reversed by viral clearance.</description><identifier>ISSN: 1529-2908</identifier><identifier>EISSN: 1529-2916</identifier><identifier>DOI: 10.1038/s41590-020-00817-w</identifier><identifier>PMID: 33398179</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>631/250/1619 ; 631/250/1619/554 ; 631/250/254 ; 631/250/255 ; 631/250/255/234 ; Antigens ; Antigens, Viral - immunology ; Antiviral Agents - therapeutic use ; Biomedical and Life Sciences ; Biomedicine ; CD8 antigen ; CD8-Positive T-Lymphocytes - immunology ; CD8-Positive T-Lymphocytes - metabolism ; CD8-Positive T-Lymphocytes - virology ; Chronic infection ; Epitopes ; Gene Expression Profiling ; Gene Regulatory Networks ; Hepacivirus - drug effects ; Hepacivirus - immunology ; Hepatitis ; Hepatitis C ; Hepatitis C, Chronic - drug therapy ; Hepatitis C, Chronic - genetics ; Hepatitis C, Chronic - immunology ; Hepatitis C, Chronic - virology ; Host-Pathogen Interactions ; Humans ; Immunologic Memory - genetics ; Immunological memory ; Immunology ; Infectious Diseases ; Interferon ; Lymphocytes ; Lymphocytes T ; Memory cells ; Phenotype ; Remission Induction ; Single-Cell Analysis ; Transcriptome ; Treatment Outcome</subject><ispartof>Nature immunology, 2021-02, Vol.22 (2), p.229-239</ispartof><rights>The Author(s), under exclusive licence to Springer Nature America, Inc. 2021</rights><rights>The Author(s), under exclusive licence to Springer Nature America, Inc. 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-f5107de5814966e3a21de96d782167769b25f21e61b1c0998e86e194581fe2863</citedby><cites>FETCH-LOGICAL-c375t-f5107de5814966e3a21de96d782167769b25f21e61b1c0998e86e194581fe2863</cites><orcidid>0000-0002-3364-5898 ; 0000-0002-1195-055X ; 0000-0001-5601-9307 ; 0000-0001-7351-1387 ; 0000-0003-1417-4135 ; 0000-0001-7036-342X ; 0000-0002-0034-4036 ; 0000-0001-8410-8833 ; 0000-0001-9416-2737</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/s41590-020-00817-w$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/s41590-020-00817-w$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33398179$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hensel, Nina</creatorcontrib><creatorcontrib>Gu, Zuguang</creatorcontrib><creatorcontrib>Sagar</creatorcontrib><creatorcontrib>Wieland, Dominik</creatorcontrib><creatorcontrib>Jechow, Katharina</creatorcontrib><creatorcontrib>Kemming, Janine</creatorcontrib><creatorcontrib>Llewellyn-Lacey, Sian</creatorcontrib><creatorcontrib>Gostick, Emma</creatorcontrib><creatorcontrib>Sogukpinar, Oezlem</creatorcontrib><creatorcontrib>Emmerich, Florian</creatorcontrib><creatorcontrib>Price, David A.</creatorcontrib><creatorcontrib>Bengsch, Bertram</creatorcontrib><creatorcontrib>Boettler, Tobias</creatorcontrib><creatorcontrib>Neumann-Haefelin, Christoph</creatorcontrib><creatorcontrib>Eils, Roland</creatorcontrib><creatorcontrib>Conrad, Christian</creatorcontrib><creatorcontrib>Bartenschlager, Ralf</creatorcontrib><creatorcontrib>Grün, Dominic</creatorcontrib><creatorcontrib>Ishaque, Naveed</creatorcontrib><creatorcontrib>Thimme, Robert</creatorcontrib><creatorcontrib>Hofmann, Maike</creatorcontrib><title>Memory-like HCV-specific CD8+ T cells retain a molecular scar after cure of chronic HCV infection</title><title>Nature immunology</title><addtitle>Nat Immunol</addtitle><addtitle>Nat Immunol</addtitle><description>In chronic hepatitis C virus (HCV) infection, exhausted HCV-specific CD8
+
T cells comprise memory-like and terminally exhausted subsets. However, little is known about the molecular profile and fate of these two subsets after the elimination of chronic antigen stimulation by direct-acting antiviral (DAA) therapy. Here, we report a progenitor–progeny relationship between memory-like and terminally exhausted HCV-specific CD8
+
T cells via an intermediate subset. Single-cell transcriptomics implicated that memory-like cells are maintained and terminally exhausted cells are lost after DAA-mediated cure, resulting in a memory polarization of the overall HCV-specific CD8
+
T cell response. However, an exhausted core signature of memory-like CD8
+
T cells was still detectable, including, to a smaller extent, in HCV-specific CD8
+
T cells targeting variant epitopes. These results identify a molecular signature of T cell exhaustion that is maintained as a chronic scar in HCV-specific CD8
+
T cells even after the cessation of chronic antigen stimulation.
Thimme and colleagues identify a molecular signature of T cell exhaustion resembling a ‘chronic scar’ that is imprinted in hepatitis C virus–specific CD8
+
T cells and cannot simply be reversed by viral clearance.</description><subject>631/250/1619</subject><subject>631/250/1619/554</subject><subject>631/250/254</subject><subject>631/250/255</subject><subject>631/250/255/234</subject><subject>Antigens</subject><subject>Antigens, Viral - immunology</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>CD8 antigen</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>CD8-Positive T-Lymphocytes - metabolism</subject><subject>CD8-Positive T-Lymphocytes - virology</subject><subject>Chronic infection</subject><subject>Epitopes</subject><subject>Gene Expression Profiling</subject><subject>Gene Regulatory Networks</subject><subject>Hepacivirus - drug effects</subject><subject>Hepacivirus - immunology</subject><subject>Hepatitis</subject><subject>Hepatitis C</subject><subject>Hepatitis C, Chronic - drug therapy</subject><subject>Hepatitis C, Chronic - genetics</subject><subject>Hepatitis C, Chronic - immunology</subject><subject>Hepatitis C, Chronic - virology</subject><subject>Host-Pathogen Interactions</subject><subject>Humans</subject><subject>Immunologic Memory - genetics</subject><subject>Immunological memory</subject><subject>Immunology</subject><subject>Infectious Diseases</subject><subject>Interferon</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Memory cells</subject><subject>Phenotype</subject><subject>Remission Induction</subject><subject>Single-Cell Analysis</subject><subject>Transcriptome</subject><subject>Treatment 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HCV-specific CD8+ T cells retain a molecular scar after cure of chronic HCV infection</title><author>Hensel, Nina ; Gu, Zuguang ; Sagar ; Wieland, Dominik ; Jechow, Katharina ; Kemming, Janine ; Llewellyn-Lacey, Sian ; Gostick, Emma ; Sogukpinar, Oezlem ; Emmerich, Florian ; Price, David A. ; Bengsch, Bertram ; Boettler, Tobias ; Neumann-Haefelin, Christoph ; Eils, Roland ; Conrad, Christian ; Bartenschlager, Ralf ; Grün, Dominic ; Ishaque, Naveed ; Thimme, Robert ; Hofmann, Maike</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-f5107de5814966e3a21de96d782167769b25f21e61b1c0998e86e194581fe2863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>631/250/1619</topic><topic>631/250/1619/554</topic><topic>631/250/254</topic><topic>631/250/255</topic><topic>631/250/255/234</topic><topic>Antigens</topic><topic>Antigens, Viral - immunology</topic><topic>Antiviral Agents - therapeutic use</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>CD8 antigen</topic><topic>CD8-Positive T-Lymphocytes - immunology</topic><topic>CD8-Positive T-Lymphocytes - metabolism</topic><topic>CD8-Positive T-Lymphocytes - virology</topic><topic>Chronic infection</topic><topic>Epitopes</topic><topic>Gene Expression Profiling</topic><topic>Gene Regulatory Networks</topic><topic>Hepacivirus - drug effects</topic><topic>Hepacivirus - immunology</topic><topic>Hepatitis</topic><topic>Hepatitis C</topic><topic>Hepatitis C, Chronic - drug therapy</topic><topic>Hepatitis C, Chronic - genetics</topic><topic>Hepatitis C, Chronic - immunology</topic><topic>Hepatitis C, Chronic - virology</topic><topic>Host-Pathogen Interactions</topic><topic>Humans</topic><topic>Immunologic Memory - genetics</topic><topic>Immunological memory</topic><topic>Immunology</topic><topic>Infectious Diseases</topic><topic>Interferon</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Memory cells</topic><topic>Phenotype</topic><topic>Remission Induction</topic><topic>Single-Cell Analysis</topic><topic>Transcriptome</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hensel, Nina</creatorcontrib><creatorcontrib>Gu, Zuguang</creatorcontrib><creatorcontrib>Sagar</creatorcontrib><creatorcontrib>Wieland, Dominik</creatorcontrib><creatorcontrib>Jechow, Katharina</creatorcontrib><creatorcontrib>Kemming, Janine</creatorcontrib><creatorcontrib>Llewellyn-Lacey, Sian</creatorcontrib><creatorcontrib>Gostick, Emma</creatorcontrib><creatorcontrib>Sogukpinar, Oezlem</creatorcontrib><creatorcontrib>Emmerich, Florian</creatorcontrib><creatorcontrib>Price, David A.</creatorcontrib><creatorcontrib>Bengsch, Bertram</creatorcontrib><creatorcontrib>Boettler, Tobias</creatorcontrib><creatorcontrib>Neumann-Haefelin, 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immunology</jtitle><stitle>Nat Immunol</stitle><addtitle>Nat Immunol</addtitle><date>2021-02-01</date><risdate>2021</risdate><volume>22</volume><issue>2</issue><spage>229</spage><epage>239</epage><pages>229-239</pages><issn>1529-2908</issn><eissn>1529-2916</eissn><abstract>In chronic hepatitis C virus (HCV) infection, exhausted HCV-specific CD8
+
T cells comprise memory-like and terminally exhausted subsets. However, little is known about the molecular profile and fate of these two subsets after the elimination of chronic antigen stimulation by direct-acting antiviral (DAA) therapy. Here, we report a progenitor–progeny relationship between memory-like and terminally exhausted HCV-specific CD8
+
T cells via an intermediate subset. Single-cell transcriptomics implicated that memory-like cells are maintained and terminally exhausted cells are lost after DAA-mediated cure, resulting in a memory polarization of the overall HCV-specific CD8
+
T cell response. However, an exhausted core signature of memory-like CD8
+
T cells was still detectable, including, to a smaller extent, in HCV-specific CD8
+
T cells targeting variant epitopes. These results identify a molecular signature of T cell exhaustion that is maintained as a chronic scar in HCV-specific CD8
+
T cells even after the cessation of chronic antigen stimulation.
Thimme and colleagues identify a molecular signature of T cell exhaustion resembling a ‘chronic scar’ that is imprinted in hepatitis C virus–specific CD8
+
T cells and cannot simply be reversed by viral clearance.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>33398179</pmid><doi>10.1038/s41590-020-00817-w</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-3364-5898</orcidid><orcidid>https://orcid.org/0000-0002-1195-055X</orcidid><orcidid>https://orcid.org/0000-0001-5601-9307</orcidid><orcidid>https://orcid.org/0000-0001-7351-1387</orcidid><orcidid>https://orcid.org/0000-0003-1417-4135</orcidid><orcidid>https://orcid.org/0000-0001-7036-342X</orcidid><orcidid>https://orcid.org/0000-0002-0034-4036</orcidid><orcidid>https://orcid.org/0000-0001-8410-8833</orcidid><orcidid>https://orcid.org/0000-0001-9416-2737</orcidid></addata></record> |
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source | MEDLINE; SpringerLink Journals; Nature |
subjects | 631/250/1619 631/250/1619/554 631/250/254 631/250/255 631/250/255/234 Antigens Antigens, Viral - immunology Antiviral Agents - therapeutic use Biomedical and Life Sciences Biomedicine CD8 antigen CD8-Positive T-Lymphocytes - immunology CD8-Positive T-Lymphocytes - metabolism CD8-Positive T-Lymphocytes - virology Chronic infection Epitopes Gene Expression Profiling Gene Regulatory Networks Hepacivirus - drug effects Hepacivirus - immunology Hepatitis Hepatitis C Hepatitis C, Chronic - drug therapy Hepatitis C, Chronic - genetics Hepatitis C, Chronic - immunology Hepatitis C, Chronic - virology Host-Pathogen Interactions Humans Immunologic Memory - genetics Immunological memory Immunology Infectious Diseases Interferon Lymphocytes Lymphocytes T Memory cells Phenotype Remission Induction Single-Cell Analysis Transcriptome Treatment Outcome |
title | Memory-like HCV-specific CD8+ T cells retain a molecular scar after cure of chronic HCV infection |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-26T11%3A11%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Memory-like%20HCV-specific%20CD8+%20T%20cells%20retain%20a%20molecular%20scar%20after%20cure%20of%20chronic%20HCV%20infection&rft.jtitle=Nature%20immunology&rft.au=Hensel,%20Nina&rft.date=2021-02-01&rft.volume=22&rft.issue=2&rft.spage=229&rft.epage=239&rft.pages=229-239&rft.issn=1529-2908&rft.eissn=1529-2916&rft_id=info:doi/10.1038/s41590-020-00817-w&rft_dat=%3Cproquest_cross%3E2480546717%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2480546717&rft_id=info:pmid/33398179&rfr_iscdi=true |