| Literature DB >> 35641155 |
Adrian M Shields1, Ariharan Anantharachagan2, Gururaj Arumugakani3, Kenneth Baker4, Sameer Bahal5, Helen Baxendale6, William Bermingham7, Malini Bhole8, Evon Boules9, Philip Bright10, Charu Chopra11, Lucy Cliffe12, Betsy Cleave12, John Dempster13, Lisa Devlin14, Fatima Dhalla15, Lavanya Diwakar16, Elizabeth Drewe12, Christopher Duncan17, Magdalena Dziadzio18, Suzanne Elcombe19, Shuayb Elkhalifa20, Andrew Gennery21, Harichandrana Ghanta22, Sarah Goddard16, Sofia Grigoriadou23, Scott Hackett24, Grant Hayman25, Richard Herriot26, Archana Herwadkar20, Aarnoud Huissoon7, Rashmi Jain15, Stephen Jolles27, Sarah Johnston10, Sujoy Khan28, James Laffan25, Peter Lane1, Lucy Leeman29, David M Lowe30,5, Shanti Mahabir31, Dylan James Mac Lochlainn15, Elizabeth McDermott12, Siraj Misbah15, Fiona Moghaddas10, Hadeil Morsi15, Sai Murng25, Sadia Noorani32, Rachael O'Brien33, Smita Patel15, Arthur Price31, Tasneem Rahman25, Suranjith Seneviratne30, Anna Shrimpton9, Catherine Stroud19, Moira Thomas34, Katie Townsend25, Prashantha Vaitla12, Nisha Verma30, Anthony Williams22, Siobhan O Burns30,5, Sinisa Savic3, Alex G Richter1.
Abstract
In March 2020, the United Kingdom Primary Immunodeficiency Network (UKPIN) established a registry of cases to collate the outcomes of individuals with PID and SID following SARS-CoV-2 infection and treatment. A total of 310 cases of SARS-CoV-2 infection in individuals with PID or SID have now been reported in the UK. The overall mortality within the cohort was 17.7% (n = 55/310). Individuals with CVID demonstrated an infection fatality rate (IFR) of 18.3% (n = 17/93), individuals with PID receiving IgRT had an IFR of 16.3% (n = 26/159) and individuals with SID, an IFR of 27.2% (n = 25/92). Individuals with PID and SID had higher inpatient mortality and died at a younger age than the general population. Increasing age, low pre-SARS-CoV-2 infection lymphocyte count and the presence of common co-morbidities increased the risk of mortality in PID. Access to specific COVID-19 treatments in this cohort was limited: only 22.9% (n = 33/144) of patients admitted to the hospital received dexamethasone, remdesivir, an anti-SARS-CoV-2 antibody-based therapeutic (e.g. REGN-COV2 or convalescent plasma) or tocilizumab as a monotherapy or in combination. Dexamethasone, remdesivir, and anti-SARS-CoV-2 antibody-based therapeutics appeared efficacious in PID and SID. Compared to the general population, individuals with PID or SID are at high risk of mortality following SARS-CoV-2 infection. Increasing age, low baseline lymphocyte count, and the presence of co-morbidities are additional risk factors for poor outcome in this cohort.Entities:
Keywords: COVID-19; SARS-CoV-2; hypogammaglobulinemia; inborn errors of immunity; lymphopenia; primary immunodeficiencies; secondary immunodeficiencies
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Year: 2022 PMID: 35641155 PMCID: PMC8807296 DOI: 10.1093/cei/uxac008
Source DB: PubMed Journal: Clin Exp Immunol ISSN: 0009-9104 Impact factor: 5.732