MAIT cell activation and dynamics associated with COVID-19 disease severity
Severe COVID-19 is characterized by excessive inflammation of the lower airways. The balance of protective versus pathological immune responses in COVID-19 is incompletely understood. Mucosa-associated invariant T (MAIT) cells are antimicrobial T cells that recognize bacterial metabolites, and can a...
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creator | Parrot, Tiphaine Gorin, Jean-Baptiste Ponzetta, Andrea Maleki, Kimia T Kammann, Tobias Emgård, Johanna Perez-Potti, André Sekine, Takuya Rivera-Ballesteros, Olga Gredmark-Russ, Sara Rooyackers, Olav Folkesson, Elin Eriksson, Lars I Norrby-Teglund, Anna Ljunggren, Hans-Gustaf Björkström, Niklas K Aleman, Soo Buggert, Marcus Klingström, Jonas Strålin, Kristoffer Sandberg, Johan K |
description | Severe COVID-19 is characterized by excessive inflammation of the lower airways. The balance of protective versus pathological immune responses in COVID-19 is incompletely understood. Mucosa-associated invariant T (MAIT) cells are antimicrobial T cells that recognize bacterial metabolites, and can also function as innate-like sensors and mediators of antiviral responses. Here, we investigated the MAIT cell compartment in COVID-19 patients with moderate and severe disease, as well as in convalescence. We show profound and preferential decline in MAIT cells in the circulation of patients with active disease paired with strong activation. Furthermore, transcriptomic analyses indicated significant MAIT cell enrichment and pro-inflammatory IL-17A bias in the airways. Unsupervised analysis identified MAIT cell CD69
and CXCR3
immunotypes associated with poor clinical outcome. MAIT cell levels normalized in the convalescent phase, consistent with dynamic recruitment to the tissues and later release back into the circulation when disease is resolved. These findings indicate that MAIT cells are engaged in the immune response against SARS-CoV-2 and suggest their possible involvement in COVID-19 immunopathogenesis. |
doi_str_mv | 10.1126/sciimmunol.abe1670 |
format | Article |
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and CXCR3
immunotypes associated with poor clinical outcome. MAIT cell levels normalized in the convalescent phase, consistent with dynamic recruitment to the tissues and later release back into the circulation when disease is resolved. These findings indicate that MAIT cells are engaged in the immune response against SARS-CoV-2 and suggest their possible involvement in COVID-19 immunopathogenesis.</description><identifier>ISSN: 2470-9468</identifier><identifier>EISSN: 2470-9468</identifier><identifier>DOI: 10.1126/sciimmunol.abe1670</identifier><identifier>PMID: 32989174</identifier><language>eng</language><publisher>United States: American Association for the Advancement of Science</publisher><subject>Adult ; Aged ; Antigens, CD - metabolism ; Antigens, Differentiation, T-Lymphocyte - metabolism ; Betacoronavirus - immunology ; Coronavirus ; Coronavirus Infections - immunology ; Coronavirus Infections - pathology ; COVID-19 ; Female ; Host Microbe Interactions ; Humans ; Immunity, Innate - immunology ; Infectious Disease ; Inflammation - immunology ; Interleukin-17 - metabolism ; Lectins, C-Type - metabolism ; Lymphocyte Activation - immunology ; Male ; Middle Aged ; Mucosal-Associated Invariant T Cells - immunology ; Pandemics ; Pneumonia, Viral - immunology ; Pneumonia, Viral - pathology ; Receptors, CXCR3 - metabolism ; SARS-CoV-2 ; SciImmunol reports ; Young Adult</subject><ispartof>Science immunology, 2020-09, Vol.5 (51)</ispartof><rights>Copyright © 2020, American Association for the Advancement of Science.</rights><rights>Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). 2020 The Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c517t-55a1637767f997d638d8a7ce5830ece8ba71a1cf0e54772c119a44606208b9a3</citedby><cites>FETCH-LOGICAL-c517t-55a1637767f997d638d8a7ce5830ece8ba71a1cf0e54772c119a44606208b9a3</cites><orcidid>0000-0002-3391-5448 ; 0000-0001-9372-1795 ; 0000-0002-5998-5700 ; 0000-0002-8433-036X ; 0000-0002-6585-6235 ; 0000-0002-6275-0750 ; 0000-0001-7649-0593 ; 0000-0001-9076-1441 ; 0000-0003-0633-1719 ; 0000-0001-9625-6825 ; 0000-0002-0967-076X ; 0000-0001-6949-4270 ; 0000-0003-4605-1375 ; 0000-0003-3224-802X ; 0000-0002-8801-3169 ; 0000-0002-2446-4323 ; 0000-0001-5382-5477</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,550,776,881</link.rule.ids><linktorsrc>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:145376449$$EView_record_in_Swedish_Publication_Index_(SWEPUB)$$FView_record_in_$$GSwedish_Publication_Index_(SWEPUB)$$Hfree_for_read</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32989174$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:145376449$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Parrot, Tiphaine</creatorcontrib><creatorcontrib>Gorin, Jean-Baptiste</creatorcontrib><creatorcontrib>Ponzetta, Andrea</creatorcontrib><creatorcontrib>Maleki, Kimia T</creatorcontrib><creatorcontrib>Kammann, Tobias</creatorcontrib><creatorcontrib>Emgård, Johanna</creatorcontrib><creatorcontrib>Perez-Potti, André</creatorcontrib><creatorcontrib>Sekine, Takuya</creatorcontrib><creatorcontrib>Rivera-Ballesteros, Olga</creatorcontrib><creatorcontrib>Gredmark-Russ, Sara</creatorcontrib><creatorcontrib>Rooyackers, Olav</creatorcontrib><creatorcontrib>Folkesson, Elin</creatorcontrib><creatorcontrib>Eriksson, Lars I</creatorcontrib><creatorcontrib>Norrby-Teglund, Anna</creatorcontrib><creatorcontrib>Ljunggren, Hans-Gustaf</creatorcontrib><creatorcontrib>Björkström, Niklas K</creatorcontrib><creatorcontrib>Aleman, Soo</creatorcontrib><creatorcontrib>Buggert, Marcus</creatorcontrib><creatorcontrib>Klingström, Jonas</creatorcontrib><creatorcontrib>Strålin, Kristoffer</creatorcontrib><creatorcontrib>Sandberg, Johan K</creatorcontrib><creatorcontrib>Karolinska COVID-19 Study Group</creatorcontrib><creatorcontrib>the Karolinska COVID-19 Study Group</creatorcontrib><title>MAIT cell activation and dynamics associated with COVID-19 disease severity</title><title>Science immunology</title><addtitle>Sci Immunol</addtitle><description>Severe COVID-19 is characterized by excessive inflammation of the lower airways. The balance of protective versus pathological immune responses in COVID-19 is incompletely understood. Mucosa-associated invariant T (MAIT) cells are antimicrobial T cells that recognize bacterial metabolites, and can also function as innate-like sensors and mediators of antiviral responses. Here, we investigated the MAIT cell compartment in COVID-19 patients with moderate and severe disease, as well as in convalescence. We show profound and preferential decline in MAIT cells in the circulation of patients with active disease paired with strong activation. Furthermore, transcriptomic analyses indicated significant MAIT cell enrichment and pro-inflammatory IL-17A bias in the airways. Unsupervised analysis identified MAIT cell CD69
and CXCR3
immunotypes associated with poor clinical outcome. MAIT cell levels normalized in the convalescent phase, consistent with dynamic recruitment to the tissues and later release back into the circulation when disease is resolved. These findings indicate that MAIT cells are engaged in the immune response against SARS-CoV-2 and suggest their possible involvement in COVID-19 immunopathogenesis.</description><subject>Adult</subject><subject>Aged</subject><subject>Antigens, CD - metabolism</subject><subject>Antigens, Differentiation, T-Lymphocyte - metabolism</subject><subject>Betacoronavirus - immunology</subject><subject>Coronavirus</subject><subject>Coronavirus Infections - immunology</subject><subject>Coronavirus Infections - pathology</subject><subject>COVID-19</subject><subject>Female</subject><subject>Host Microbe Interactions</subject><subject>Humans</subject><subject>Immunity, Innate - immunology</subject><subject>Infectious Disease</subject><subject>Inflammation - immunology</subject><subject>Interleukin-17 - metabolism</subject><subject>Lectins, C-Type - metabolism</subject><subject>Lymphocyte Activation - immunology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mucosal-Associated Invariant T Cells - immunology</subject><subject>Pandemics</subject><subject>Pneumonia, Viral - immunology</subject><subject>Pneumonia, Viral - pathology</subject><subject>Receptors, CXCR3 - metabolism</subject><subject>SARS-CoV-2</subject><subject>SciImmunol reports</subject><subject>Young Adult</subject><issn>2470-9468</issn><issn>2470-9468</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>D8T</sourceid><recordid>eNpVUctOKzEMjdBFgIAfYIGyvJuBZJKJkw0S6uVRAWJTsY3cjAuBeXAn01b9e6Zqea1s2edh-TB2IsWZlLk5TyHGup43bXWGU5IGxA47yDWIzGlj__zo99lxSq9CCGlzCUbvsX2VO-sk6AN293A5nvBAVcUx9HGBfWwbjk3Jy1WDdQyJY0ptiNhTyZexf-Gjx6fxv0w6XsZEmIgnWlAX-9UR251hleh4Ww_Z5PpqMrrN7h9vxqPL-ywUEvqsKFAaBWBg5hyURtnSIgQqrBIUyE4RJMowE1RogDxI6VBrI0wu7NShOmTZRjYt6X0-9e9drLFb-Raj347eho68NgCFG_AXG_ywqakM1PQdVr9ovzdNfPHP7cKDLUA5NQj83Qp07f85pd7XMa1fhg218-RzrUFJJdzaK99AQ9em1NHsy0YKv87Nf-fmt7kNpNOfB35RPlNSH7ttmCg</recordid><startdate>20200928</startdate><enddate>20200928</enddate><creator>Parrot, Tiphaine</creator><creator>Gorin, Jean-Baptiste</creator><creator>Ponzetta, Andrea</creator><creator>Maleki, Kimia T</creator><creator>Kammann, Tobias</creator><creator>Emgård, Johanna</creator><creator>Perez-Potti, André</creator><creator>Sekine, Takuya</creator><creator>Rivera-Ballesteros, Olga</creator><creator>Gredmark-Russ, Sara</creator><creator>Rooyackers, Olav</creator><creator>Folkesson, Elin</creator><creator>Eriksson, Lars I</creator><creator>Norrby-Teglund, Anna</creator><creator>Ljunggren, Hans-Gustaf</creator><creator>Björkström, Niklas K</creator><creator>Aleman, Soo</creator><creator>Buggert, Marcus</creator><creator>Klingström, Jonas</creator><creator>Strålin, Kristoffer</creator><creator>Sandberg, Johan K</creator><general>American Association for the Advancement of Science</general><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>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>ZZAVC</scope><orcidid>https://orcid.org/0000-0002-3391-5448</orcidid><orcidid>https://orcid.org/0000-0001-9372-1795</orcidid><orcidid>https://orcid.org/0000-0002-5998-5700</orcidid><orcidid>https://orcid.org/0000-0002-8433-036X</orcidid><orcidid>https://orcid.org/0000-0002-6585-6235</orcidid><orcidid>https://orcid.org/0000-0002-6275-0750</orcidid><orcidid>https://orcid.org/0000-0001-7649-0593</orcidid><orcidid>https://orcid.org/0000-0001-9076-1441</orcidid><orcidid>https://orcid.org/0000-0003-0633-1719</orcidid><orcidid>https://orcid.org/0000-0001-9625-6825</orcidid><orcidid>https://orcid.org/0000-0002-0967-076X</orcidid><orcidid>https://orcid.org/0000-0001-6949-4270</orcidid><orcidid>https://orcid.org/0000-0003-4605-1375</orcidid><orcidid>https://orcid.org/0000-0003-3224-802X</orcidid><orcidid>https://orcid.org/0000-0002-8801-3169</orcidid><orcidid>https://orcid.org/0000-0002-2446-4323</orcidid><orcidid>https://orcid.org/0000-0001-5382-5477</orcidid></search><sort><creationdate>20200928</creationdate><title>MAIT cell activation and dynamics associated with COVID-19 disease severity</title><author>Parrot, Tiphaine ; Gorin, Jean-Baptiste ; Ponzetta, Andrea ; Maleki, Kimia T ; Kammann, Tobias ; Emgård, Johanna ; Perez-Potti, André ; Sekine, Takuya ; Rivera-Ballesteros, Olga ; Gredmark-Russ, Sara ; Rooyackers, Olav ; Folkesson, Elin ; Eriksson, Lars I ; Norrby-Teglund, Anna ; Ljunggren, Hans-Gustaf ; Björkström, Niklas K ; Aleman, Soo ; Buggert, Marcus ; Klingström, Jonas ; Strålin, Kristoffer ; Sandberg, Johan K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c517t-55a1637767f997d638d8a7ce5830ece8ba71a1cf0e54772c119a44606208b9a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antigens, CD - metabolism</topic><topic>Antigens, Differentiation, T-Lymphocyte - metabolism</topic><topic>Betacoronavirus - immunology</topic><topic>Coronavirus</topic><topic>Coronavirus Infections - immunology</topic><topic>Coronavirus Infections - pathology</topic><topic>COVID-19</topic><topic>Female</topic><topic>Host Microbe Interactions</topic><topic>Humans</topic><topic>Immunity, Innate - immunology</topic><topic>Infectious Disease</topic><topic>Inflammation - immunology</topic><topic>Interleukin-17 - metabolism</topic><topic>Lectins, C-Type - metabolism</topic><topic>Lymphocyte Activation - immunology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mucosal-Associated Invariant T Cells - immunology</topic><topic>Pandemics</topic><topic>Pneumonia, Viral - immunology</topic><topic>Pneumonia, Viral - pathology</topic><topic>Receptors, CXCR3 - metabolism</topic><topic>SARS-CoV-2</topic><topic>SciImmunol reports</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Parrot, Tiphaine</creatorcontrib><creatorcontrib>Gorin, Jean-Baptiste</creatorcontrib><creatorcontrib>Ponzetta, Andrea</creatorcontrib><creatorcontrib>Maleki, Kimia T</creatorcontrib><creatorcontrib>Kammann, Tobias</creatorcontrib><creatorcontrib>Emgård, Johanna</creatorcontrib><creatorcontrib>Perez-Potti, André</creatorcontrib><creatorcontrib>Sekine, Takuya</creatorcontrib><creatorcontrib>Rivera-Ballesteros, Olga</creatorcontrib><creatorcontrib>Gredmark-Russ, Sara</creatorcontrib><creatorcontrib>Rooyackers, Olav</creatorcontrib><creatorcontrib>Folkesson, Elin</creatorcontrib><creatorcontrib>Eriksson, Lars I</creatorcontrib><creatorcontrib>Norrby-Teglund, Anna</creatorcontrib><creatorcontrib>Ljunggren, Hans-Gustaf</creatorcontrib><creatorcontrib>Björkström, Niklas K</creatorcontrib><creatorcontrib>Aleman, Soo</creatorcontrib><creatorcontrib>Buggert, Marcus</creatorcontrib><creatorcontrib>Klingström, Jonas</creatorcontrib><creatorcontrib>Strålin, Kristoffer</creatorcontrib><creatorcontrib>Sandberg, Johan K</creatorcontrib><creatorcontrib>Karolinska COVID-19 Study Group</creatorcontrib><creatorcontrib>the Karolinska COVID-19 Study Group</creatorcontrib><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>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><jtitle>Science immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Parrot, Tiphaine</au><au>Gorin, Jean-Baptiste</au><au>Ponzetta, Andrea</au><au>Maleki, Kimia T</au><au>Kammann, Tobias</au><au>Emgård, Johanna</au><au>Perez-Potti, André</au><au>Sekine, Takuya</au><au>Rivera-Ballesteros, Olga</au><au>Gredmark-Russ, Sara</au><au>Rooyackers, Olav</au><au>Folkesson, Elin</au><au>Eriksson, Lars I</au><au>Norrby-Teglund, Anna</au><au>Ljunggren, Hans-Gustaf</au><au>Björkström, Niklas K</au><au>Aleman, Soo</au><au>Buggert, Marcus</au><au>Klingström, Jonas</au><au>Strålin, Kristoffer</au><au>Sandberg, Johan K</au><aucorp>Karolinska COVID-19 Study Group</aucorp><aucorp>the Karolinska COVID-19 Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MAIT cell activation and dynamics associated with COVID-19 disease severity</atitle><jtitle>Science immunology</jtitle><addtitle>Sci Immunol</addtitle><date>2020-09-28</date><risdate>2020</risdate><volume>5</volume><issue>51</issue><issn>2470-9468</issn><eissn>2470-9468</eissn><abstract>Severe COVID-19 is characterized by excessive inflammation of the lower airways. The balance of protective versus pathological immune responses in COVID-19 is incompletely understood. Mucosa-associated invariant T (MAIT) cells are antimicrobial T cells that recognize bacterial metabolites, and can also function as innate-like sensors and mediators of antiviral responses. Here, we investigated the MAIT cell compartment in COVID-19 patients with moderate and severe disease, as well as in convalescence. We show profound and preferential decline in MAIT cells in the circulation of patients with active disease paired with strong activation. Furthermore, transcriptomic analyses indicated significant MAIT cell enrichment and pro-inflammatory IL-17A bias in the airways. Unsupervised analysis identified MAIT cell CD69
and CXCR3
immunotypes associated with poor clinical outcome. MAIT cell levels normalized in the convalescent phase, consistent with dynamic recruitment to the tissues and later release back into the circulation when disease is resolved. These findings indicate that MAIT cells are engaged in the immune response against SARS-CoV-2 and suggest their possible involvement in COVID-19 immunopathogenesis.</abstract><cop>United States</cop><pub>American Association for the Advancement of Science</pub><pmid>32989174</pmid><doi>10.1126/sciimmunol.abe1670</doi><orcidid>https://orcid.org/0000-0002-3391-5448</orcidid><orcidid>https://orcid.org/0000-0001-9372-1795</orcidid><orcidid>https://orcid.org/0000-0002-5998-5700</orcidid><orcidid>https://orcid.org/0000-0002-8433-036X</orcidid><orcidid>https://orcid.org/0000-0002-6585-6235</orcidid><orcidid>https://orcid.org/0000-0002-6275-0750</orcidid><orcidid>https://orcid.org/0000-0001-7649-0593</orcidid><orcidid>https://orcid.org/0000-0001-9076-1441</orcidid><orcidid>https://orcid.org/0000-0003-0633-1719</orcidid><orcidid>https://orcid.org/0000-0001-9625-6825</orcidid><orcidid>https://orcid.org/0000-0002-0967-076X</orcidid><orcidid>https://orcid.org/0000-0001-6949-4270</orcidid><orcidid>https://orcid.org/0000-0003-4605-1375</orcidid><orcidid>https://orcid.org/0000-0003-3224-802X</orcidid><orcidid>https://orcid.org/0000-0002-8801-3169</orcidid><orcidid>https://orcid.org/0000-0002-2446-4323</orcidid><orcidid>https://orcid.org/0000-0001-5382-5477</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Antigens, CD - metabolism Antigens, Differentiation, T-Lymphocyte - metabolism Betacoronavirus - immunology Coronavirus Coronavirus Infections - immunology Coronavirus Infections - pathology COVID-19 Female Host Microbe Interactions Humans Immunity, Innate - immunology Infectious Disease Inflammation - immunology Interleukin-17 - metabolism Lectins, C-Type - metabolism Lymphocyte Activation - immunology Male Middle Aged Mucosal-Associated Invariant T Cells - immunology Pandemics Pneumonia, Viral - immunology Pneumonia, Viral - pathology Receptors, CXCR3 - metabolism SARS-CoV-2 SciImmunol reports Young Adult |
title | MAIT cell activation and dynamics associated with COVID-19 disease severity |
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