SARS-CoV-2 breakthrough infections among vaccinated individuals with rheumatic disease: results from the COVID-19 Global Rheumatology Alliance provider registry
Author:
Liew JeanORCID, Gianfrancesco Milena, Harrison Carly, Izadi ZaraORCID, Rush Stephanie, Lawson-Tovey SaskiaORCID, Jacobsohn Lindsay, Ja Clairissa, Hyrich Kimme L, Gossec LaureORCID, Strangfeld AnjaORCID, Carmona LoretoORCID, Schäfer MartinORCID, Frãzao-Mateus Elsa, Bulina Inita, Stafford Frances, Tufan Abdurrahman, Graver Christine, Yardımcı Gözde KübraORCID, Zepa Julija, Al Emadi Samar, Cook Claire, Abutiban Fatemah, Dey Dfiza, Katigbak Genevieve, Kaufman Lauren, Kowalski Emily, Martínez-Martínez Marco Ulises, Patel Naomi J, Reyes-Cordero Greta, Salido Evelyn, Smith Ellison, Snow David, Sparks JeffreyORCID, Wise Leanna, Bhana Suleman, Gore-Massy Monique, Grainger Rebecca, Hausmann JonathanORCID, Sirotich EmilyORCID, Sufka Paul, Wallace Zachary, Machado Pedro MORCID, Robinson Philip CORCID, Yazdany Jinoos
Abstract
ObjectiveWhile COVID-19 vaccination prevents severe infections, poor immunogenicity in immunocompromised people threatens vaccine effectiveness. We analysed the clinical characteristics of patients with rheumatic disease who developed breakthrough COVID-19 after vaccination against SARS-CoV-2.MethodsWe included people partially or fully vaccinated against SARS-CoV-2 who developed COVID-19 between 5 January and 30 September 2021 and were reported to the Global Rheumatology Alliance registry. Breakthrough infections were defined as occurring ≥14 days after completion of the vaccination series, specifically 14 days after the second dose in a two-dose series or 14 days after a single-dose vaccine. We analysed patients’ demographic and clinical characteristics and COVID-19 symptoms and outcomes.ResultsSARS-CoV-2 infection was reported in 197 partially or fully vaccinated people with rheumatic disease (mean age 54 years, 77% female, 56% white). The majority (n=140/197, 71%) received messenger RNA vaccines. Among the fully vaccinated (n=87), infection occurred a mean of 112 (±60) days after the second vaccine dose. Among those fully vaccinated and hospitalised (n=22, age range 36–83 years), nine had used B cell-depleting therapy (BCDT), with six as monotherapy, at the time of vaccination. Three were on mycophenolate. The majority (n=14/22, 64%) were not taking systemic glucocorticoids. Eight patients had pre-existing lung disease and five patients died.ConclusionMore than half of fully vaccinated individuals with breakthrough infections requiring hospitalisation were on BCDT or mycophenolate. Further risk mitigation strategies are likely needed to protect this selected high-risk population.
Funder
Rheumatology Research Foundation National Institute for Health Research NIH Clinical Center
Subject
Immunology,Immunology and Allergy,Rheumatology
Cited by
38 articles.
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