PD-1-Expressing SARS-CoV-2-Specific CD8+ T Cells Are Not Exhausted, but Functional in Patients with COVID-19

Memory T cell responses have been demonstrated in COVID-19 convalescents, but ex vivo phenotypes of SARS-CoV-2-specific T cells have been unclear. We detected SARS-CoV-2-specific CD8+ T cells by MHC class I multimer staining and examined their phenotypes and functions in acute and convalescent COVID...

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Veröffentlicht in:Immunity (Cambridge, Mass.) Mass.), 2021-01, Vol.54 (1), p.44-52.e3
Hauptverfasser: Rha, Min-Seok, Jeong, Hye Won, Ko, Jae-Hoon, Choi, Seong Jin, Seo, In-Ho, Lee, Jeong Seok, Sa, Moa, Kim, A Reum, Joo, Eun-Jeong, Ahn, Jin Young, Kim, Jung Ho, Song, Kyoung-Ho, Kim, Eu Suk, Oh, Dong Hyun, Ahn, Mi Young, Choi, Hee Kyoung, Jeon, Ji Hoon, Choi, Jae-Phil, Kim, Hong Bin, Kim, Young Keun, Park, Su-Hyung, Choi, Won Suk, Choi, Jun Yong, Peck, Kyong Ran, Shin, Eui-Cheol
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container_end_page 52.e3
container_issue 1
container_start_page 44
container_title Immunity (Cambridge, Mass.)
container_volume 54
creator Rha, Min-Seok
Jeong, Hye Won
Ko, Jae-Hoon
Choi, Seong Jin
Seo, In-Ho
Lee, Jeong Seok
Sa, Moa
Kim, A Reum
Joo, Eun-Jeong
Ahn, Jin Young
Kim, Jung Ho
Song, Kyoung-Ho
Kim, Eu Suk
Oh, Dong Hyun
Ahn, Mi Young
Choi, Hee Kyoung
Jeon, Ji Hoon
Choi, Jae-Phil
Kim, Hong Bin
Kim, Young Keun
Park, Su-Hyung
Choi, Won Suk
Choi, Jun Yong
Peck, Kyong Ran
Shin, Eui-Cheol
description Memory T cell responses have been demonstrated in COVID-19 convalescents, but ex vivo phenotypes of SARS-CoV-2-specific T cells have been unclear. We detected SARS-CoV-2-specific CD8+ T cells by MHC class I multimer staining and examined their phenotypes and functions in acute and convalescent COVID-19. Multimer+ cells exhibited early differentiated effector-memory phenotypes in the early convalescent phase. The frequency of stem-like memory cells was increased among multimer+ cells in the late convalescent phase. Cytokine secretion assays combined with MHC class I multimer staining revealed that the proportion of interferon-γ (IFN-γ)-producing cells was significantly lower among SARS-CoV-2-specific CD8+ T cells than those specific to influenza A virus. Importantly, the proportion of IFN-γ-producing cells was higher in PD-1+ cells than PD-1− cells among multimer+ cells, indicating that PD-1-expressing, SARS-CoV-2-specific CD8+ T cells are not exhausted, but functional. Our current findings provide information for understanding of SARS-CoV-2-specific CD8+ T cells elicited by infection or vaccination. [Display omitted] •SARS-CoV-2-specific CD8+ T cells are effector memory cells in convalescents•CCR7+CD45RA+ cells are increased among SARS-CoV-2-specific cells in the late phase•SARS-CoV-2-specific CD8+ T cells have fewer IFN-γ+ cells than flu-specific cells•PD-1-expressing SARS-CoV-2-specific CD8+ T cells are not exhausted but functional T cell responses have been demonstrated in COVID-19 patients, but ex vivo phenotypes and functions of SARS-CoV-2-specific T cells remain unclear. Rha et al. examined SARS-CoV-2-specific CD8+ T cells in acute and convalescent COVID-19 patients using MHC class I multimers, finding that PD-1-expressing SARS-CoV-2-specific CD8+ T cells are not exhausted but functional.
doi_str_mv 10.1016/j.immuni.2020.12.002
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We detected SARS-CoV-2-specific CD8+ T cells by MHC class I multimer staining and examined their phenotypes and functions in acute and convalescent COVID-19. Multimer+ cells exhibited early differentiated effector-memory phenotypes in the early convalescent phase. The frequency of stem-like memory cells was increased among multimer+ cells in the late convalescent phase. Cytokine secretion assays combined with MHC class I multimer staining revealed that the proportion of interferon-γ (IFN-γ)-producing cells was significantly lower among SARS-CoV-2-specific CD8+ T cells than those specific to influenza A virus. Importantly, the proportion of IFN-γ-producing cells was higher in PD-1+ cells than PD-1− cells among multimer+ cells, indicating that PD-1-expressing, SARS-CoV-2-specific CD8+ T cells are not exhausted, but functional. Our current findings provide information for understanding of SARS-CoV-2-specific CD8+ T cells elicited by infection or vaccination. [Display omitted] •SARS-CoV-2-specific CD8+ T cells are effector memory cells in convalescents•CCR7+CD45RA+ cells are increased among SARS-CoV-2-specific cells in the late phase•SARS-CoV-2-specific CD8+ T cells have fewer IFN-γ+ cells than flu-specific cells•PD-1-expressing SARS-CoV-2-specific CD8+ T cells are not exhausted but functional T cell responses have been demonstrated in COVID-19 patients, but ex vivo phenotypes and functions of SARS-CoV-2-specific T cells remain unclear. Rha et al. examined SARS-CoV-2-specific CD8+ T cells in acute and convalescent COVID-19 patients using MHC class I multimers, finding that PD-1-expressing SARS-CoV-2-specific CD8+ T cells are not exhausted but functional.</description><identifier>ISSN: 1074-7613</identifier><identifier>EISSN: 1097-4180</identifier><identifier>DOI: 10.1016/j.immuni.2020.12.002</identifier><identifier>PMID: 33338412</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Acute-Phase Reaction - immunology ; Acute-Phase Reaction - virology ; CD8 antigen ; CD8+ T cell ; CD8-Positive T-Lymphocytes - immunology ; Cell differentiation ; Convalescence ; Coronaviruses ; COVID-19 ; COVID-19 - immunology ; COVID-19 - pathology ; COVID-19 - virology ; Cytokines ; Disease ; Effector cells ; Epitopes, T-Lymphocyte ; Genotype &amp; phenotype ; Histocompatibility Antigens Class I - immunology ; Humans ; IFN-γ ; Immunologic Memory ; Immunological memory ; Immunophenotyping ; Infections ; Influenza A ; Interferon ; Interferon-gamma - metabolism ; Lymphocyte Activation ; Lymphocytes ; Lymphocytes T ; Major histocompatibility complex ; Memory cells ; Memory T cell ; MHC class I multimer ; PD-1 ; PD-1 protein ; Phenotypes ; Population ; Programmed Cell Death 1 Receptor - metabolism ; Proteins ; Public health ; SARS-CoV-2 ; SARS-CoV-2 - immunology ; Severe acute respiratory syndrome ; Severe acute respiratory syndrome coronavirus 2 ; Staining ; Vaccination ; Viral diseases ; Viral infections ; Viral Load ; Viruses ; γ-Interferon</subject><ispartof>Immunity (Cambridge, Mass.), 2021-01, Vol.54 (1), p.44-52.e3</ispartof><rights>2020 Elsevier Inc.</rights><rights>Copyright © 2020 Elsevier Inc. 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Elsevier Inc.</rights><rights>2020 Elsevier Inc. 2020 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c598t-2c778e2e09379df45a8873dc6f68b8be0ebf82cf4521ffa2d82eb57af8a55df73</citedby><cites>FETCH-LOGICAL-c598t-2c778e2e09379df45a8873dc6f68b8be0ebf82cf4521ffa2d82eb57af8a55df73</cites><orcidid>0000-0002-2775-3315 ; 0000-0001-6363-7736 ; 0000-0002-5033-3482 ; 0000-0002-1063-8476 ; 0000-0001-5874-4764 ; 0000-0001-8280-7745 ; 0000-0003-3140-1336 ; 0000-0002-2120-6265 ; 0000-0001-6262-372X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.immuni.2020.12.002$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,315,781,785,886,3551,27926,27927,45997</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33338412$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rha, Min-Seok</creatorcontrib><creatorcontrib>Jeong, Hye Won</creatorcontrib><creatorcontrib>Ko, Jae-Hoon</creatorcontrib><creatorcontrib>Choi, Seong Jin</creatorcontrib><creatorcontrib>Seo, In-Ho</creatorcontrib><creatorcontrib>Lee, Jeong Seok</creatorcontrib><creatorcontrib>Sa, Moa</creatorcontrib><creatorcontrib>Kim, A Reum</creatorcontrib><creatorcontrib>Joo, Eun-Jeong</creatorcontrib><creatorcontrib>Ahn, Jin Young</creatorcontrib><creatorcontrib>Kim, Jung Ho</creatorcontrib><creatorcontrib>Song, Kyoung-Ho</creatorcontrib><creatorcontrib>Kim, Eu Suk</creatorcontrib><creatorcontrib>Oh, Dong Hyun</creatorcontrib><creatorcontrib>Ahn, Mi Young</creatorcontrib><creatorcontrib>Choi, Hee Kyoung</creatorcontrib><creatorcontrib>Jeon, Ji Hoon</creatorcontrib><creatorcontrib>Choi, Jae-Phil</creatorcontrib><creatorcontrib>Kim, Hong Bin</creatorcontrib><creatorcontrib>Kim, Young Keun</creatorcontrib><creatorcontrib>Park, Su-Hyung</creatorcontrib><creatorcontrib>Choi, Won Suk</creatorcontrib><creatorcontrib>Choi, Jun Yong</creatorcontrib><creatorcontrib>Peck, Kyong Ran</creatorcontrib><creatorcontrib>Shin, Eui-Cheol</creatorcontrib><title>PD-1-Expressing SARS-CoV-2-Specific CD8+ T Cells Are Not Exhausted, but Functional in Patients with COVID-19</title><title>Immunity (Cambridge, Mass.)</title><addtitle>Immunity</addtitle><description>Memory T cell responses have been demonstrated in COVID-19 convalescents, but ex vivo phenotypes of SARS-CoV-2-specific T cells have been unclear. We detected SARS-CoV-2-specific CD8+ T cells by MHC class I multimer staining and examined their phenotypes and functions in acute and convalescent COVID-19. Multimer+ cells exhibited early differentiated effector-memory phenotypes in the early convalescent phase. The frequency of stem-like memory cells was increased among multimer+ cells in the late convalescent phase. Cytokine secretion assays combined with MHC class I multimer staining revealed that the proportion of interferon-γ (IFN-γ)-producing cells was significantly lower among SARS-CoV-2-specific CD8+ T cells than those specific to influenza A virus. Importantly, the proportion of IFN-γ-producing cells was higher in PD-1+ cells than PD-1− cells among multimer+ cells, indicating that PD-1-expressing, SARS-CoV-2-specific CD8+ T cells are not exhausted, but functional. Our current findings provide information for understanding of SARS-CoV-2-specific CD8+ T cells elicited by infection or vaccination. [Display omitted] •SARS-CoV-2-specific CD8+ T cells are effector memory cells in convalescents•CCR7+CD45RA+ cells are increased among SARS-CoV-2-specific cells in the late phase•SARS-CoV-2-specific CD8+ T cells have fewer IFN-γ+ cells than flu-specific cells•PD-1-expressing SARS-CoV-2-specific CD8+ T cells are not exhausted but functional T cell responses have been demonstrated in COVID-19 patients, but ex vivo phenotypes and functions of SARS-CoV-2-specific T cells remain unclear. 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immunology</topic><topic>Acute-Phase Reaction - virology</topic><topic>CD8 antigen</topic><topic>CD8+ T cell</topic><topic>CD8-Positive T-Lymphocytes - immunology</topic><topic>Cell differentiation</topic><topic>Convalescence</topic><topic>Coronaviruses</topic><topic>COVID-19</topic><topic>COVID-19 - immunology</topic><topic>COVID-19 - pathology</topic><topic>COVID-19 - virology</topic><topic>Cytokines</topic><topic>Disease</topic><topic>Effector cells</topic><topic>Epitopes, T-Lymphocyte</topic><topic>Genotype &amp; phenotype</topic><topic>Histocompatibility Antigens Class I - immunology</topic><topic>Humans</topic><topic>IFN-γ</topic><topic>Immunologic Memory</topic><topic>Immunological memory</topic><topic>Immunophenotyping</topic><topic>Infections</topic><topic>Influenza A</topic><topic>Interferon</topic><topic>Interferon-gamma - metabolism</topic><topic>Lymphocyte Activation</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Major histocompatibility complex</topic><topic>Memory cells</topic><topic>Memory T cell</topic><topic>MHC class I multimer</topic><topic>PD-1</topic><topic>PD-1 protein</topic><topic>Phenotypes</topic><topic>Population</topic><topic>Programmed Cell Death 1 Receptor - metabolism</topic><topic>Proteins</topic><topic>Public health</topic><topic>SARS-CoV-2</topic><topic>SARS-CoV-2 - immunology</topic><topic>Severe acute respiratory syndrome</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Staining</topic><topic>Vaccination</topic><topic>Viral diseases</topic><topic>Viral infections</topic><topic>Viral Load</topic><topic>Viruses</topic><topic>γ-Interferon</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rha, Min-Seok</creatorcontrib><creatorcontrib>Jeong, Hye Won</creatorcontrib><creatorcontrib>Ko, Jae-Hoon</creatorcontrib><creatorcontrib>Choi, Seong Jin</creatorcontrib><creatorcontrib>Seo, In-Ho</creatorcontrib><creatorcontrib>Lee, Jeong Seok</creatorcontrib><creatorcontrib>Sa, Moa</creatorcontrib><creatorcontrib>Kim, A Reum</creatorcontrib><creatorcontrib>Joo, Eun-Jeong</creatorcontrib><creatorcontrib>Ahn, Jin Young</creatorcontrib><creatorcontrib>Kim, Jung Ho</creatorcontrib><creatorcontrib>Song, Kyoung-Ho</creatorcontrib><creatorcontrib>Kim, Eu Suk</creatorcontrib><creatorcontrib>Oh, Dong Hyun</creatorcontrib><creatorcontrib>Ahn, Mi Young</creatorcontrib><creatorcontrib>Choi, Hee Kyoung</creatorcontrib><creatorcontrib>Jeon, Ji Hoon</creatorcontrib><creatorcontrib>Choi, Jae-Phil</creatorcontrib><creatorcontrib>Kim, Hong Bin</creatorcontrib><creatorcontrib>Kim, Young Keun</creatorcontrib><creatorcontrib>Park, Su-Hyung</creatorcontrib><creatorcontrib>Choi, Won Suk</creatorcontrib><creatorcontrib>Choi, Jun Yong</creatorcontrib><creatorcontrib>Peck, Kyong Ran</creatorcontrib><creatorcontrib>Shin, Eui-Cheol</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Immunity (Cambridge, Mass.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rha, Min-Seok</au><au>Jeong, Hye Won</au><au>Ko, Jae-Hoon</au><au>Choi, Seong Jin</au><au>Seo, In-Ho</au><au>Lee, Jeong Seok</au><au>Sa, Moa</au><au>Kim, A Reum</au><au>Joo, Eun-Jeong</au><au>Ahn, Jin Young</au><au>Kim, Jung Ho</au><au>Song, Kyoung-Ho</au><au>Kim, Eu Suk</au><au>Oh, Dong Hyun</au><au>Ahn, Mi Young</au><au>Choi, Hee Kyoung</au><au>Jeon, Ji Hoon</au><au>Choi, Jae-Phil</au><au>Kim, Hong Bin</au><au>Kim, Young Keun</au><au>Park, Su-Hyung</au><au>Choi, Won Suk</au><au>Choi, Jun Yong</au><au>Peck, Kyong Ran</au><au>Shin, Eui-Cheol</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PD-1-Expressing SARS-CoV-2-Specific CD8+ T Cells Are Not Exhausted, but Functional in Patients with COVID-19</atitle><jtitle>Immunity (Cambridge, Mass.)</jtitle><addtitle>Immunity</addtitle><date>2021-01-12</date><risdate>2021</risdate><volume>54</volume><issue>1</issue><spage>44</spage><epage>52.e3</epage><pages>44-52.e3</pages><issn>1074-7613</issn><eissn>1097-4180</eissn><abstract>Memory T cell responses have been demonstrated in COVID-19 convalescents, but ex vivo phenotypes of SARS-CoV-2-specific T cells have been unclear. We detected SARS-CoV-2-specific CD8+ T cells by MHC class I multimer staining and examined their phenotypes and functions in acute and convalescent COVID-19. Multimer+ cells exhibited early differentiated effector-memory phenotypes in the early convalescent phase. The frequency of stem-like memory cells was increased among multimer+ cells in the late convalescent phase. Cytokine secretion assays combined with MHC class I multimer staining revealed that the proportion of interferon-γ (IFN-γ)-producing cells was significantly lower among SARS-CoV-2-specific CD8+ T cells than those specific to influenza A virus. Importantly, the proportion of IFN-γ-producing cells was higher in PD-1+ cells than PD-1− cells among multimer+ cells, indicating that PD-1-expressing, SARS-CoV-2-specific CD8+ T cells are not exhausted, but functional. Our current findings provide information for understanding of SARS-CoV-2-specific CD8+ T cells elicited by infection or vaccination. [Display omitted] •SARS-CoV-2-specific CD8+ T cells are effector memory cells in convalescents•CCR7+CD45RA+ cells are increased among SARS-CoV-2-specific cells in the late phase•SARS-CoV-2-specific CD8+ T cells have fewer IFN-γ+ cells than flu-specific cells•PD-1-expressing SARS-CoV-2-specific CD8+ T cells are not exhausted but functional T cell responses have been demonstrated in COVID-19 patients, but ex vivo phenotypes and functions of SARS-CoV-2-specific T cells remain unclear. Rha et al. examined SARS-CoV-2-specific CD8+ T cells in acute and convalescent COVID-19 patients using MHC class I multimers, finding that PD-1-expressing SARS-CoV-2-specific CD8+ T cells are not exhausted but functional.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>33338412</pmid><doi>10.1016/j.immuni.2020.12.002</doi><orcidid>https://orcid.org/0000-0002-2775-3315</orcidid><orcidid>https://orcid.org/0000-0001-6363-7736</orcidid><orcidid>https://orcid.org/0000-0002-5033-3482</orcidid><orcidid>https://orcid.org/0000-0002-1063-8476</orcidid><orcidid>https://orcid.org/0000-0001-5874-4764</orcidid><orcidid>https://orcid.org/0000-0001-8280-7745</orcidid><orcidid>https://orcid.org/0000-0003-3140-1336</orcidid><orcidid>https://orcid.org/0000-0002-2120-6265</orcidid><orcidid>https://orcid.org/0000-0001-6262-372X</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1074-7613
ispartof Immunity (Cambridge, Mass.), 2021-01, Vol.54 (1), p.44-52.e3
issn 1074-7613
1097-4180
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7834198
source MEDLINE; Cell Press Free Archives; Access via ScienceDirect (Elsevier); EZB-FREE-00999 freely available EZB journals
subjects Acute-Phase Reaction - immunology
Acute-Phase Reaction - virology
CD8 antigen
CD8+ T cell
CD8-Positive T-Lymphocytes - immunology
Cell differentiation
Convalescence
Coronaviruses
COVID-19
COVID-19 - immunology
COVID-19 - pathology
COVID-19 - virology
Cytokines
Disease
Effector cells
Epitopes, T-Lymphocyte
Genotype & phenotype
Histocompatibility Antigens Class I - immunology
Humans
IFN-γ
Immunologic Memory
Immunological memory
Immunophenotyping
Infections
Influenza A
Interferon
Interferon-gamma - metabolism
Lymphocyte Activation
Lymphocytes
Lymphocytes T
Major histocompatibility complex
Memory cells
Memory T cell
MHC class I multimer
PD-1
PD-1 protein
Phenotypes
Population
Programmed Cell Death 1 Receptor - metabolism
Proteins
Public health
SARS-CoV-2
SARS-CoV-2 - immunology
Severe acute respiratory syndrome
Severe acute respiratory syndrome coronavirus 2
Staining
Vaccination
Viral diseases
Viral infections
Viral Load
Viruses
γ-Interferon
title PD-1-Expressing SARS-CoV-2-Specific CD8+ T Cells Are Not Exhausted, but Functional in Patients with COVID-19
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