Journal of Translational Autoimmunity (Jan 2021)

Characteristics of COVID-19 infection and antibody formation in patients known at a tertiary immunology department

  • Niels A.D. Guchelaar,
  • Jan A.M. van Laar,
  • Maud A.W. Hermans,
  • Tim B. van der Houwen,
  • Sibel Atmaca,
  • Maurits S. van Maaren,
  • Zana Brkic,
  • Paul L.A. van Daele,
  • Virgil A.S.H. Dalm,
  • P. Martin van Hagen,
  • Saskia M. Rombach

Journal volume & issue
Vol. 4
p. 100084

Abstract

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Background: Knowledge about COVID-19 infections is expanding, although knowledge about the disease course and antibody formation in patients with an auto-immune disease or immunodeficiency is not fully unraveled yet. It could be hypothesized that immunodeficient patients, due to immunosuppressive drugs or their disease, have a more severe disease course due to their immunocompromised state. However, it could also be hypothesized that some of the immunosuppressive drugs protect against a hyperinflammatory state. Methods: We collected data on the incidence of COVID-19, disease course and SARS-CoV-2 antibody formation in COVID-19 positive patients in a cohort of patients (n ​= ​4497) known at the Clinical Immunology outpatient clinic in a tertiary care hospital in the Netherlands. Results: In the first six months of the pandemic, 16 patients were identified with COVID-19, 14 by nasal swab PCR, and 2 patients by SARS-CoV-2 antibodies. Eight patients were admitted to the hospital. SARS-CoV-2 antibodies were measured in 8 patients and were detectable in all, including one patient on B-cell ablative therapy and one patient with Common Variable Immunodeficiency Disorder. Conclusion: This study indicates that the disease course differs among immunocompromised patients, independently of (dis)continuation of immunosuppressive drugs. Antibody production for SARS-CoV-2 in immunocompromised patients was shown. More research needs to be conducted to confirm these observations and guidelines regarding (dis)continuation of immunosuppressive drugs in COVID-19 positive immunocompromised patients should be developed.

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