2020
DOI: 10.1016/j.anai.2020.04.033
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The clinical observation of a patient with common variable immunodeficiency diagnosed as having coronavirus disease 2019

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Cited by 44 publications
(63 citation statements)
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“…There were 3 reports 22 - 24 describing a total of 10 COVID-19 patients with pre-existing PAD (Table 1 ). Of these, 6 patients had common variable immunodeficiency (CVID), 3 had X-linked agammaglobulinemia (XLA) due to loss-of-function mutations in the Bruton tyrosine kinase (BTK), and 1 patient had autosomal recessive agammaglobulinemia (ARA), the etiology of which is unknown.…”
Section: Resultsmentioning
confidence: 99%
“…There were 3 reports 22 - 24 describing a total of 10 COVID-19 patients with pre-existing PAD (Table 1 ). Of these, 6 patients had common variable immunodeficiency (CVID), 3 had X-linked agammaglobulinemia (XLA) due to loss-of-function mutations in the Bruton tyrosine kinase (BTK), and 1 patient had autosomal recessive agammaglobulinemia (ARA), the etiology of which is unknown.…”
Section: Resultsmentioning
confidence: 99%
“…Although immunodeficiency is described as a risk factor for coronavirus disease 2019 (COVID-19), limited data are available regarding CVID. Of note, 3 recent reports describe mostly positive outcomes in patients with CVID who were diagnosed as having COVID-19, 1 , 2 , 3 with only 1 fatality. 3 All these patients had adequate immunoglobulin G (IgG) levels at the time of COVID-19 diagnosis.…”
mentioning
confidence: 99%
“… 3 All these patients had adequate immunoglobulin G (IgG) levels at the time of COVID-19 diagnosis. 1 , 2 , 3 We present a case of a patient with a history of CVID and severely low IgG levels owing to a lapse in immunoglobulin replacement therapy, who died of complications related to COVID-19 despite receiving convalescent plasma and high-dose intravenous immunoglobulin (IVIG).…”
mentioning
confidence: 99%
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“…The behavior of COVID-19 in patients with IEI might help dissect the immune response to SARS-Cov2. A few cases of adults with COVID-19 and predominantly antibody deficiencies have been reported 3,4 ; some of them developed acute respiratory distress syndrome (ARDS), while some had a milder course of illness. Based on what we know, innate immune defects in genes involved in type 1 interferon response (such as IRF7, IRF9, TLR3) are the most likely candidates to result in severe disease and death in patients with flu-like virus infection 5 .…”
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confidence: 99%