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10.1016/j.jtauto.2021.100084

http://scihub22266oqcxt.onion/10.1016/j.jtauto.2021.100084
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suck abstract from ncbi


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pmid33532723      J+Transl+Autoimmun 2021 ; 4 (ä): 100084
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  • Characteristics of COVID-19 infection and antibody formation in patients known at a tertiary immunology department #MMPMID33532723
  • Guchelaar NAD; van Laar JAM; Hermans MAW; van der Houwen TB; Atmaca S; van Maaren MS; Brkic Z; van Daele PLA; Dalm VASH; van Hagen PM; Rombach SM
  • J Transl Autoimmun 2021[]; 4 (ä): 100084 PMID33532723show ga
  • 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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