SARS-CoV-2-specific serological and functional T cell immune responses during acute and early COVID-19 convalescence in solid organ transplant patients
© 2021 The American Society of Transplantation and the American Society of Transplant Surgeons..
The description of protective humoral and T cell immune responses specific against SARS-CoV-2 has been reported among immunocompetent (IC) individuals developing COVID-19 infection. However, its characterization and determinants of poorer outcomes among the at-risk solid organ transplant (SOT) patient population have not been thoroughly investigated. Cytokine-producing T cell responses, such as IFN-γ, IL-2, IFN-γ/IL-2, IL-6, IL-21, and IL-5, against main immunogenic SARS-CoV-2 antigens and IgM/IgG serological immunity were tracked in SOT (n = 28) during acute infection and at two consecutive time points over the following 40 days of convalescence and were compared to matched IC (n = 16) patients admitted with similar moderate/severe COVID-19. We describe the development of a robust serological and functional T cell immune responses against SARS-CoV-2 among SOT patients, similar to IC patients during early convalescence. However, at the infection onset, SOT displayed lower IgG seroconversion rates (77% vs. 100%; p = .044), despite no differences on IgG titers, and a trend toward decreased SARS-CoV-2-reactive T cell frequencies, especially against the membrane protein (7 [0-34] vs. 113 [15-245], p = .011, 2 [0-9] vs. 45 [5-74], p = .009, and 0 [0-2] vs. 13 [1-24], p = .020, IFN-γ, IL-2, and IFN-γ/IL-2 spots, respectively). In summary, our data suggest that despite a certain initial delay, SOT population achieve comparable functional immune responses than the general population after moderate/severe COVID-19.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2021 |
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Erschienen: |
2021 |
Enthalten in: |
Zur Gesamtaufnahme - volume:21 |
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Enthalten in: |
American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons - 21(2021), 8 vom: 07. Aug., Seite 2749-2761 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Favà, Alexandre [VerfasserIn] |
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Links: |
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Anmerkungen: |
Date Completed 10.08.2021 Date Revised 24.01.2023 published: Print-Electronic Citation Status MEDLINE |
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doi: |
10.1111/ajt.16570 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM323123112 |
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520 | |a © 2021 The American Society of Transplantation and the American Society of Transplant Surgeons. | ||
520 | |a The description of protective humoral and T cell immune responses specific against SARS-CoV-2 has been reported among immunocompetent (IC) individuals developing COVID-19 infection. However, its characterization and determinants of poorer outcomes among the at-risk solid organ transplant (SOT) patient population have not been thoroughly investigated. Cytokine-producing T cell responses, such as IFN-γ, IL-2, IFN-γ/IL-2, IL-6, IL-21, and IL-5, against main immunogenic SARS-CoV-2 antigens and IgM/IgG serological immunity were tracked in SOT (n = 28) during acute infection and at two consecutive time points over the following 40 days of convalescence and were compared to matched IC (n = 16) patients admitted with similar moderate/severe COVID-19. We describe the development of a robust serological and functional T cell immune responses against SARS-CoV-2 among SOT patients, similar to IC patients during early convalescence. However, at the infection onset, SOT displayed lower IgG seroconversion rates (77% vs. 100%; p = .044), despite no differences on IgG titers, and a trend toward decreased SARS-CoV-2-reactive T cell frequencies, especially against the membrane protein (7 [0-34] vs. 113 [15-245], p = .011, 2 [0-9] vs. 45 [5-74], p = .009, and 0 [0-2] vs. 13 [1-24], p = .020, IFN-γ, IL-2, and IFN-γ/IL-2 spots, respectively). In summary, our data suggest that despite a certain initial delay, SOT population achieve comparable functional immune responses than the general population after moderate/severe COVID-19 | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 4 | |a COVID-19 infection | |
650 | 4 | |a T cell biology | |
650 | 4 | |a adaptive immunity | |
650 | 4 | |a basic (laboratory) research / science | |
650 | 4 | |a clinical research / practice | |
650 | 4 | |a heart transplantation / cardiology | |
650 | 4 | |a infection and infectious agents | |
650 | 4 | |a kidney transplantation / nephrology | |
650 | 4 | |a liver transplantation / hepatology | |
650 | 4 | |a solid organ transplantation | |
650 | 7 | |a Antibodies, Viral |2 NLM | |
700 | 1 | |a Donadeu, Laura |e verfasserin |4 aut | |
700 | 1 | |a Sabé, Nuria |e verfasserin |4 aut | |
700 | 1 | |a Pernin, Vincent |e verfasserin |4 aut | |
700 | 1 | |a González-Costello, José |e verfasserin |4 aut | |
700 | 1 | |a Lladó, Laura |e verfasserin |4 aut | |
700 | 1 | |a Meneghini, Maria |e verfasserin |4 aut | |
700 | 1 | |a Charmetant, Xavier |e verfasserin |4 aut | |
700 | 1 | |a García-Romero, Elena |e verfasserin |4 aut | |
700 | 1 | |a Cachero, Alba |e verfasserin |4 aut | |
700 | 1 | |a Torija, Alba |e verfasserin |4 aut | |
700 | 1 | |a Rodriguez-Urquia, Ronny |e verfasserin |4 aut | |
700 | 1 | |a Crespo, Elena |e verfasserin |4 aut | |
700 | 1 | |a Teubel, Iris |e verfasserin |4 aut | |
700 | 1 | |a Melilli, Edoardo |e verfasserin |4 aut | |
700 | 1 | |a Montero, Nuria |e verfasserin |4 aut | |
700 | 1 | |a Manonelles, Anna |e verfasserin |4 aut | |
700 | 1 | |a Preyer, Rosemarie |e verfasserin |4 aut | |
700 | 1 | |a Strecker, Kevin |e verfasserin |4 aut | |
700 | 1 | |a Ovize, Anne |e verfasserin |4 aut | |
700 | 1 | |a Lozano, Juan J |e verfasserin |4 aut | |
700 | 1 | |a Sidorova, Julia |e verfasserin |4 aut | |
700 | 1 | |a Cruzado, Josep M |e verfasserin |4 aut | |
700 | 1 | |a Le Quintrec, Moglie |e verfasserin |4 aut | |
700 | 1 | |a Thaunat, Olivier |e verfasserin |4 aut | |
700 | 1 | |a Bestard, Oriol |e verfasserin |4 aut | |
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