Cited 182 times in
PD-1-Expressing SARS-CoV-2-Specific CD8 + T Cells Are Not Exhausted, but Functional in Patients with COVID-19
DC Field | Value | Language |
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dc.contributor.author | 김정호 | - |
dc.contributor.author | 신의철 | - |
dc.contributor.author | 안진영 | - |
dc.contributor.author | 최준용 | - |
dc.date.accessioned | 2021-04-29T16:55:06Z | - |
dc.date.available | 2021-04-29T16:55:06Z | - |
dc.date.issued | 2021-01 | - |
dc.identifier.issn | 1074-7613 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/182087 | - |
dc.description.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. | - |
dc.description.statementOfResponsibility | open | - |
dc.language | English | - |
dc.publisher | Cell Press | - |
dc.relation.isPartOf | IMMUNITY | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Acute-Phase Reaction / immunology | - |
dc.subject.MESH | Acute-Phase Reaction / virology | - |
dc.subject.MESH | CD8-Positive T-Lymphocytes / immunology* | - |
dc.subject.MESH | COVID-19 / immunology* | - |
dc.subject.MESH | COVID-19 / pathology | - |
dc.subject.MESH | COVID-19 / virology | - |
dc.subject.MESH | Convalescence | - |
dc.subject.MESH | Epitopes, T-Lymphocyte | - |
dc.subject.MESH | Histocompatibility Antigens Class I / immunology | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Immunologic Memory | - |
dc.subject.MESH | Immunophenotyping | - |
dc.subject.MESH | Interferon-gamma / metabolism | - |
dc.subject.MESH | Lymphocyte Activation | - |
dc.subject.MESH | Programmed Cell Death 1 Receptor / metabolism* | - |
dc.subject.MESH | SARS-CoV-2 / immunology* | - |
dc.subject.MESH | Viral Load | - |
dc.title | PD-1-Expressing SARS-CoV-2-Specific CD8 + T Cells Are Not Exhausted, but Functional in Patients with COVID-19 | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
dc.contributor.googleauthor | Min-Seok Rha | - |
dc.contributor.googleauthor | Hye Won Jeong | - |
dc.contributor.googleauthor | Jae-Hoon Ko | - |
dc.contributor.googleauthor | Seong Jin Choi | - |
dc.contributor.googleauthor | In-Ho Seo | - |
dc.contributor.googleauthor | Jeong Seok Lee | - |
dc.contributor.googleauthor | Moa Sa | - |
dc.contributor.googleauthor | A Reum Kim | - |
dc.contributor.googleauthor | Eun-Jeong Joo | - |
dc.contributor.googleauthor | Jin Young Ahn | - |
dc.contributor.googleauthor | Jung Ho Kim | - |
dc.contributor.googleauthor | Kyoung-Ho Song | - |
dc.contributor.googleauthor | Eu Suk Kim | - |
dc.contributor.googleauthor | Dong Hyun Oh | - |
dc.contributor.googleauthor | Mi Young Ahn | - |
dc.contributor.googleauthor | Hee Kyoung Choi | - |
dc.contributor.googleauthor | Ji Hoon Jeon | - |
dc.contributor.googleauthor | Jae-Phil Choi | - |
dc.contributor.googleauthor | Hong Bin Kim | - |
dc.contributor.googleauthor | Young Keun Kim | - |
dc.contributor.googleauthor | Su-Hyung Park | - |
dc.contributor.googleauthor | Won Suk Choi | - |
dc.contributor.googleauthor | Jun Yong Choi | - |
dc.contributor.googleauthor | Kyong Ran Peck | - |
dc.contributor.googleauthor | Eui-Cheol Shin | - |
dc.identifier.doi | 10.1016/j.immuni.2020.12.002 | - |
dc.contributor.localId | A00902 | - |
dc.contributor.localId | A02137 | - |
dc.contributor.localId | A02267 | - |
dc.contributor.localId | A04191 | - |
dc.relation.journalcode | J01034 | - |
dc.identifier.eissn | 1097-4180 | - |
dc.identifier.pmid | 33338412 | - |
dc.subject.keyword | CD8(+) T cell | - |
dc.subject.keyword | COVID-19 | - |
dc.subject.keyword | IFN-γ | - |
dc.subject.keyword | MHC class I multimer | - |
dc.subject.keyword | Memory T cell | - |
dc.subject.keyword | PD-1 | - |
dc.subject.keyword | SARS-CoV-2 | - |
dc.contributor.alternativeName | Kim, Jung Ho | - |
dc.contributor.affiliatedAuthor | 김정호 | - |
dc.contributor.affiliatedAuthor | 신의철 | - |
dc.contributor.affiliatedAuthor | 안진영 | - |
dc.contributor.affiliatedAuthor | 최준용 | - |
dc.citation.volume | 54 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 44 | - |
dc.citation.endPage | 52.e3 | - |
dc.identifier.bibliographicCitation | IMMUNITY, Vol.54(1) : 44-52.e3, 2021-01 | - |
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