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|a 10.1016/j.clim.2022.108991
|2 doi
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|a pubmed24n1533.xml
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|a (DE-627)NLM338942386
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|a (NLM)35364330
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|a (PII)S1521-6616(22)00072-9
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Kaneko, Naoki
|e verfasserin
|4 aut
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|a Temporal changes in T cell subsets and expansion of cytotoxic CD4+ T cells in the lungs in severe COVID-19
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|c 2022
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 18.04.2022
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|a Date Revised 14.09.2024
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|a published: Print-Electronic
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|a UpdateOf: medRxiv. 2021 Mar 26:2021.03.23.21253885. doi: 10.1101/2021.03.23.21253885. - PMID 33791730
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|a Citation Status MEDLINE
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|a Copyright © 2022. Published by Elsevier Inc.
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|a Many studies have been performed in severe COVID-19 on immune cells in the circulation and on cells obtained by bronchoalveolar lavage. Most studies have tended to provide relative information rather than a quantitative view, and it is a combination of approaches by various groups that is helping the field build a picture of the mechanisms that drive severe lung disease. Approaches employed to date have not revealed information on lung parenchymal T cell subsets in severe COVID-19. Therefore, we sought to examine early and late T cell subset alterations in the lungs and draining lymph nodes in severe COVID-19 using a rapid autopsy protocol and quantitative imaging approaches. Here, we have established that cytotoxic CD4+ T cells (CD4 + CTLs) increase in the lungs, draining lymph nodes and blood as COVID-19 progresses. CD4 + CTLs are prominently expanded in the lung parenchyma in severe COVID-19. In contrast CD8+ T cells are not prominent, exhibit increased PD-1 expression, and no obvious increase is seen in the number of Granzyme B+ CD8+ T cells in the lung parenchyma in severe COVID-19. Based on quantitative evidence for re-activation in the lung milieu, CD4 + CTLs may be as likely to drive viral clearance as CD8+ T cells and may also be contributors to lung inflammation and eventually to fibrosis in severe COVID-19
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|a Journal Article
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|a Research Support, N.I.H., Extramural
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|a Research Support, Non-U.S. Gov't
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|a CD8+ T cells
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|a COVID-19
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|a Cytotoxic CD4+ T cells
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|a Boucau, Julie
|e verfasserin
|4 aut
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1 |
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|a Kuo, Hsiao-Hsuan
|e verfasserin
|4 aut
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1 |
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|a Perugino, Cory
|e verfasserin
|4 aut
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1 |
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|a Mahajan, Vinay S
|e verfasserin
|4 aut
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1 |
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|a Farmer, Jocelyn R
|e verfasserin
|4 aut
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1 |
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|a Liu, Hang
|e verfasserin
|4 aut
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1 |
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|a Diefenbach, Thomas J
|e verfasserin
|4 aut
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1 |
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|a Piechocka-Trocha, Alicja
|e verfasserin
|4 aut
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1 |
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|a Lefteri, Kristina
|e verfasserin
|4 aut
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1 |
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|a Waring, Michael T
|e verfasserin
|4 aut
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1 |
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|a Premo, Katherine R
|e verfasserin
|4 aut
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|a Walker, Bruce D
|e verfasserin
|4 aut
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|a Li, Jonathan Z
|e verfasserin
|4 aut
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1 |
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|a Gaiha, Gaurav
|e verfasserin
|4 aut
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1 |
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|a Yu, Xu G
|e verfasserin
|4 aut
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1 |
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|a Lichterfeld, Mathias
|e verfasserin
|4 aut
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1 |
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|a Padera, Robert F
|c Jr
|e verfasserin
|4 aut
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1 |
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|a Pillai, Shiv
|e verfasserin
|4 aut
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773 |
0 |
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 237(2022) vom: 12. Apr., Seite 108991
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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|g volume:237
|g year:2022
|g day:12
|g month:04
|g pages:108991
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|u http://dx.doi.org/10.1016/j.clim.2022.108991
|3 Volltext
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|a AR
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|d 237
|j 2022
|b 12
|c 04
|h 108991
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