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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 ; Mack, Matthias

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 und 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, S. 110502.

Veröffentlichungsdatum dieses Volltextes: 29 Apr 2025 05:31
Artikel
DOI zum Zitieren dieses Dokuments: 10.5283/epub.76616


Zusammenfassung

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

DokumentenartArtikel
Titel eines Journals oder einer ZeitschriftClinical Immunology
Verlag:Elsevier
Band:277
Seitenbereich:S. 110502
Datum24 April 2025
InstitutionenMedizin > Abteilung für Nephrologie
Medizin > Lehrstuhl für Medizinische Mikrobiologie und Hygiene
Leibniz-Institut für Immuntherapie (LIT)
Projekte
Gefördert von: Bundesministerium für Bildung und Forschung (BMBF) (01EP2105A)
Identifikationsnummer
WertTyp
10.1016/j.clim.2025.110502DOI
Stichwörter / KeywordsLong-COVID, T cells, Cytokines, IL-3
Dewey-Dezimal-Klassifikation600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin
StatusVeröffentlicht
BegutachtetJa, diese Version wurde begutachtet
An der Universität Regensburg entstandenZum Teil
URN der UB Regensburgurn:nbn:de:bvb:355-epub-766162
Dokumenten-ID76616

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