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Hyper-reactivity of CD8+ T cells and high expression of IL-3 correlates with occurrence and severity of Long-COVID
Renner, Kerstin, Stauffenberg, Franz, Paulus, Moritz, Neumayer, Sophia, Winter-Köhler, Frederike, Buchtler, Simone, Schmalenberger, Daniel, Blaas, Stefan, Mohr, Arno, Pfeifer, Michael, Malfertheiner, Maximilian V., Loew, Thomas, Sester, Martina, Bals, Robert, Peterhoff, David
, Schmidt, Barbara
and Mack, Matthias
(2025)
Hyper-reactivity of CD8+ T cells and high expression of IL-3 correlates with occurrence and severity of Long-COVID.
Clinical Immunology 277, p. 110502.
Date of publication of this fulltext: 29 Apr 2025 05:31
Article
DOI to cite this document: 10.5283/epub.76616
Abstract
Following SARS-CoV-2 infection, some individuals develop Long-COVID-syndrome lasting for more than 3 months. We analyzed blood samples from patients with Long-COVID, controls without persistent symptoms following SARS-CoV-2-infection and non-infected donors without a history of infection. Long-COVID patients showed clear signs of T cell hyper-activation predominantly in the CD8+ T cell subset ...
Following SARS-CoV-2 infection, some individuals develop Long-COVID-syndrome lasting for more than 3 months. We analyzed blood samples from patients with Long-COVID, controls without persistent symptoms following SARS-CoV-2-infection and non-infected donors without a history of infection. Long-COVID patients showed clear signs of T cell hyper-activation predominantly in the CD8+ T cell subset with a 4-fold higher expression of CD25 and 2-fold more effector-memory T cells. Following polyclonal T cell stimulation, we found a 2-fold stronger upregulation of CD25 and a 7-fold higher release of IL-3 in Long-COVID. Intracellular staining revealed 5-fold more IL-3-expressing CD8+ T cells in Long-COVID, while GM-CSF, IFN-γ and IL-2 were much less upregulated. These changes correlated with the severity of Long-COVID and persisted for up to 18 months after infection. Our data reveal a pronounced and long-lasting CD8+ T cell hyper-activation and hyper-reactivity in Long-COVID and speak for a trial of T cell-immunosuppression in patients with Long-COVID.
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Details
| Item type | Article | ||||
| Journal or Publication Title | Clinical Immunology | ||||
| Publisher: | Elsevier | ||||
|---|---|---|---|---|---|
| Open Access Type: | DEAL (Elsevier) | ||||
| Volume: | 277 | ||||
| Page Range: | p. 110502 | ||||
| Date | 24 April 2025 | ||||
| Institutions | Medicine > Abteilung für Nephrologie Medicine > Lehrstuhl für Medizinische Mikrobiologie und Hygiene Leibniz Institute for Immunotherapy (LIT) | ||||
| Projects |
Funded by:
Bundesministerium für Bildung und Forschung (BMBF)
(01EP2105A)
| ||||
| Identification Number |
| ||||
| Keywords | Long-COVID, T cells, Cytokines, IL-3 | ||||
| Dewey Decimal Classification | 600 Technology > 610 Medical sciences Medicine | ||||
| Status | Published | ||||
| Refereed | Yes, this version has been refereed | ||||
| Created at the University of Regensburg | Partially | ||||
| URN of the UB Regensburg | urn:nbn:de:bvb:355-epub-766162 | ||||
| Item ID | 76616 |
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