Divergent SARS‐CoV‐2‐specific T‐and B‐cell responses in severe but not mild COVID‐19 patients

AE Oja, A Saris, CA Ghandour… - European journal of …, 2020 - Wiley Online Library
AE Oja, A Saris, CA Ghandour, NAM Kragten, BM Hogema, EJ Nossent, LMA Heunks
European journal of immunology, 2020Wiley Online Library
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 …
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.
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