Author: Abraham, Roshini S.; Marshall, Joanna M.; Kuehn, Hye Sun; Rueda, Cesar M.; Gibbs, Amber; Guider, Will; Stewart, Claire; Rosenzweig, Sergio D.; Wang, Huanyu; Jean, Sophonie; Peeples, Mark; King, Tiffany; Hunt, W. Garrett; Honegger, Jonathan R.; Ramilo, Octavio; Mustillo, Peter J.; Mejias, Asuncion; Ardura, Monica I.; Shimamura, Masako
Title: Severe SARS-CoV-2 Disease In The Context Of A NFκB2 Loss-Of-Function Pathogenic Variant Cord-id: 2qlxxt23 Document date: 2020_9_30
ID: 2qlxxt23
Snippet: Background SARS-CoV-2 is a novel coronavirus that emerged recently and has created a global pandemic. Symptomatic SARS-CoV-2 infection, termed Coronavirus disease 2019 (COVID-19), has been associated with a host of symptoms affecting numerous organ systems, including lungs, cardiovascular system, kidney, central nervous system, gastrointestinal tract and skin among others. Objective While several risk factors have been identified related to complications from and severity of COVID-19, much about
Document: Background SARS-CoV-2 is a novel coronavirus that emerged recently and has created a global pandemic. Symptomatic SARS-CoV-2 infection, termed Coronavirus disease 2019 (COVID-19), has been associated with a host of symptoms affecting numerous organ systems, including lungs, cardiovascular system, kidney, central nervous system, gastrointestinal tract and skin among others. Objective While several risk factors have been identified related to complications from and severity of COVID-19, much about the virus remains unknown. The host immune response appears to affect the outcome of disease. It is not surprising that patients with intrinsic or secondary immune compromise might be particularly susceptible to complications from SARS-CoV-2 infection. Pathogenic loss-of-function (LOF) or gain-of-function (GOF) heterozygous variants in NFκB2 have been reported to be associated with either a combined immunodeficiency (CID) or common variable immunodeficiency (CVID) phenotype. Methods We evaluated the functional consequence and immunological phenotype of a novel NFKB2 LOF variant in a 17y old male patient and describe the clinical management of SARS-CoV-2 infection in this context. Results This patient required a 2-week hospitalization for SARS-CoV-2 infection, including seven days of mechanical ventilation. We used biological therapies to avert potentially fatal acute respiratory distress syndrome and treat hyperinflammatory responses. The patient had an immunological phenotype of B cell dysregulation with decreased switched memory B cells. Despite the underlying immune dysfunction, he recovered from the infection with intense management. Conclusions This clinical case exemplifies some of the practical challenges in management of patients with SARS-CoV-2 infection, especially in the context of underlying immune dysregulation.
Search related documents:
Co phrase search for related documents- active disease and acute illness: 1, 2, 3, 4, 5, 6
- active disease and adaptive immunity: 1, 2, 3, 4
- acute illness and adaptive immunity: 1, 2, 3, 4
- acute illness and additional dose: 1
- acute illness and additional sample: 1
Co phrase search for related documents, hyperlinks ordered by date