Evidence map›Paper›PMID 33532723›Full record

ArticleJournal of translational autoimmunity2021

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 and 1 more

Abstract read
In one paragraph

Article in Journal of translational autoimmunity, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. COVID-19 and Inborn Errors of Immunity.Physiology (Bethesda, Md.) · 2022
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Niels A D GuchelaarDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Academic Center for Rare Systemic Immune Diseases, Erasmus MC University Medical Center, Rotterdam, the Netherlands.
Jan A M van LaarDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Academic Center for Rare Systemic Immune Diseases, Erasmus MC University Medical Center, Rotterdam, the Netherlands.
Maud A W HermansDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Academic Center for Rare Systemic Immune Diseases, Erasmus MC University Medical Center, Rotterdam, the Netherlands.
Tim B van der HouwenDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Academic Center for Rare Systemic Immune Diseases, Erasmus MC University Medical Center, Rotterdam, the Netherlands.
Sibel AtmacaDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Academic Center for Rare Systemic Immune Diseases, Erasmus MC University Medical Center, Rotterdam, the Netherlands.
Maurits S van MaarenDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Academic Center for Rare Systemic Immune Diseases, Erasmus MC University Medical Center, Rotterdam, the Netherlands.
Zana BrkicDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Academic Center for Rare Systemic Immune Diseases, Erasmus MC University Medical Center, Rotterdam, the Netherlands.
Paul L A van DaeleDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Academic Center for Rare Systemic Immune Diseases, Erasmus MC University Medical Center, Rotterdam, the Netherlands.
Virgil A S H DalmDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Academic Center for Rare Systemic Immune Diseases, Erasmus MC University Medical Center, Rotterdam, the Netherlands.
P Martin van HagenDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Academic Center for Rare Systemic Immune Diseases, Erasmus MC University Medical Center, Rotterdam, the Netherlands.
Saskia M RombachDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Academic Center for Rare Systemic Immune Diseases, Erasmus MC University Medical Center, Rotterdam, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundKnowledge 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.

methodsWe 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.

resultsIn 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.

conclusionThis 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.

Indexed as

AntibodiesCOVID-19ImmunocompromisedImmunologic deficiency syndromesImmunosuppressive agents

Identifiers

PMID33532723
PMCPMC7844355

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