SARS-CoV-2 infection in alpha1-antitrypsin deficiency

Alpha1-antitrypsin deficiency arises due to mutations in alpha1-antitrypsin (AAT) gene and represents the most prominent genetic predisposition to chronic obstructive pulmonary disease and emphysema. Since AAT plays important immunomodulatory and tissue-protective roles and since it was suggested to...

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Bibliographic Details
Published inRespiratory medicine Vol. 184; p. 106466
Main Authors Schneider, Carolin V., Strnad, Pavel
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.08.2021
Elsevier Limited
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Summary:Alpha1-antitrypsin deficiency arises due to mutations in alpha1-antitrypsin (AAT) gene and represents the most prominent genetic predisposition to chronic obstructive pulmonary disease and emphysema. Since AAT plays important immunomodulatory and tissue-protective roles and since it was suggested to protect from severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, we assessed this association in United Kingdom Biobank, a community-based cohort with >500,000 participants. The most common, mild AATD genotypes were associated neither with increased SARS-CoV-2 infection rates nor with increased SARS-CoV-2 fatalities, while the numbers of severe AATD cases were too low to allow definitive conclusions. •Alpha1-antitrypsin deficiency (AATD) may predispose to SARS-CoV-2 infection.•Subjects with mild AATD do not carry an increased risk of SARS-CoV-2-related injury.•We found no increased risk of SARS-CoV-2 infection or death associated with AATD.
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ISSN:0954-6111
1532-3064
1532-3064
DOI:10.1016/j.rmed.2021.106466