| Literature DB >> 33073359 |
Anna E Oja1, Anno Saris2,3, Cherien A Ghandour1, Natasja A M Kragten1, Boris M Hogema4, Esther J Nossent3,5, Leo M A Heunks3,6, Susan Cuvalay7, Ed Slot8, Federica Linty9, Francis H Swaneveld7, Hans Vrielink7, Gestur Vidarsson9, Theo Rispens10, Ellen van der Schoot9, René A W van Lier1, Anja Ten Brinke10, Pleun Hombrink1.
Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the causative agent of the current coronavirus disease 2019 (COVID-19) pandemic. Understanding the immune response that provides specific immunity but may also lead to immunopathology is crucial for the design of potential preventive and therapeutic strategies. Here, we characterized and quantified SARS-CoV-2-specific immune responses in patients with different clinical courses. Compared to individuals with a mild clinical presentation, CD4+ T-cell responses were qualitatively impaired in critically ill patients. Strikingly, however, in these patients the specific IgG antibody response was remarkably strong. Furthermore, in these critically ill patients, a massive influx of circulating T cells into the lungs was observed, overwhelming the local T-cell compartment, and indicative of vascular leakage. The observed disparate T- and B-cell responses could be indicative of a deregulated immune response in critically ill COVID-19 patients.Entities:
Keywords: CD4+ T cells; COVID-19; IgG; SARS-CoV-2; antibody response
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Year: 2020 PMID: 33073359 DOI: 10.1002/eji.202048908
Source DB: PubMed Journal: Eur J Immunol ISSN: 0014-2980 Impact factor: 5.532