z-logo
open-access-imgOpen Access
Characteristics of COVID-19 infection and antibody formation in patients known at a tertiary immunology department
Author(s) -
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 Brkić,
Paul Van Daele,
Virgil A. S. H. Dalm,
P. Martin van Hagen,
Saskia M. Rombach
Publication year - 2021
Publication title -
journal of translational autoimmunity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.199
H-Index - 3
ISSN - 2589-9090
DOI - 10.1016/j.jtauto.2021.100084
Subject(s) - medicine , antibody , disease , immunology , pandemic , incidence (geometry) , covid-19 , cohort , hydroxychloroquine , immune system , infectious disease (medical specialty) , optics , physics
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.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom