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Treatment with sotrovimab for SARS-CoV-2 infection in a cohort of high-risk kidney transplant recipients

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dc.contributor.author Villanego, Florentino
dc.contributor.author Mazuecos, Auxiliadora
dc.contributor.author Cubillo, Beatriz
dc.contributor.author José-Merino, M
dc.contributor.author Poveda, Inmaculada
dc.contributor.author Saura, Isabel-M
dc.contributor.author Segurado, Oscar
dc.contributor.author Cruzado, Leonidas
dc.contributor.author Eady, Myriam
dc.contributor.author Zarraga, Sofia
dc.contributor.author José-Aladren, M
dc.contributor.author Cabello, Sheila
dc.contributor.author López, Verónica
dc.contributor.author González, Esther
dc.contributor.author Lorenzo, Inmaculada
dc.contributor.author Espi-Reig, Jordi
dc.contributor.author Fernández, Constantino
dc.contributor.author Osma, July
dc.contributor.author Ruiz-Fuentes, MCarmen
dc.contributor.author Toapanta, Nestor
dc.contributor.author Franco, Antonio
dc.contributor.author Burballa, Carla-C
dc.contributor.author Munoz, Miguel-A
dc.contributor.author Crespo, Marta
dc.contributor.author Pascual, Julio
dc.date.accessioned 2025-11-19T15:36:59Z
dc.date.available 2025-11-19T15:36:59Z
dc.date.issued 2022-09
dc.identifier.citation Villanego F, Mazuecos A, Cubillo B, Merino MJ, Poveda I, Saura IM, et al. Treatment with sotrovimab for SARS-CoV-2 infection in a cohort of high-risk kidney transplant recipients. Clinical Kidney Journal. 22 de septiembre de 2022;15(10):1847-55.
dc.identifier.issn 2048-8505
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/21288
dc.description.abstract BACKGROUND: Sotrovimab is a neutralizing monoclonal antibody (mAb) that seems to remain active against recent severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants. The evidence on its use in kidney transplant (KT) recipients, however, is limited. METHODS: We performed a multicenter, retrospective cohort study of 82 KT patients with SARS-CoV-2 infection {coronavirus disease 2019 [COVID-19]} treated with sotrovimab. RESULTS: Median age was 63 years. Diabetes was present in 43.9% of patients, and obesity in 32.9% of patients; 48.8% of patients had an estimated glomerular filtration rate under 30 mL/minute/1.73 m(2). Additional anti-COVID-19 therapies were administered to 56 patients, especially intravenous steroids (65.9%). Sotrovimab was administered early (<5 days from the onset of the symptoms) in 46 patients (56%). Early-treated patients showed less likely progression to severe COVID-19 than those treated later, represented as a lower need for ventilator support (2.2% vs 36.1%; P < .001) or intensive care admission (2.2% vs 25%; P = .002) and COVID-19-related mortality (2.2% vs 16.7%; P = .020). In the multivariable analysis, controlling for baseline risk factors to severe COVID-19 in KT recipients, early use of sotrovimab remained as a protective factor for a composite outcome, including need for ventilator support, intensive care, and COVID-19-related mortality. No anaphylactic reactions, acute rejection episodes, impaired kidney function events, or non-kidney side effects related to sotrovimab were observed. CONCLUSIONS: Sotrovimab had an excellent safety profile, even in high-comorbidity patients and advanced chronic kidney disease stages. Earlier administration could prevent progression to severe disease, while clinical outcomes were poor in patients treated later. Larger controlled studies enrolling KT recipients are warranted to elucidate the true efficacy of monoclonal antibody therapies.
dc.language.iso eng
dc.publisher OXFORD UNIV PRESS
dc.rights Atribución/Reconocimiento-NoComercial 4.0 Internacional
dc.rights.uri https://creativecommons.org/licenses/by-nc/4.0/ *
dc.title Treatment with sotrovimab for SARS-CoV-2 infection in a cohort of high-risk kidney transplant recipients
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 36147706
dc.relation.publisherversion https://academic.oup.com/ckj/article/15/10/1847/6651282
dc.identifier.doi 10.1093/ckj/sfac177
dc.journal.title Clinical Kidney Journal
dc.identifier.essn 2048-8513


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Atribución/Reconocimiento-NoComercial 4.0 Internacional Excepto si se señala otra cosa, la licencia del ítem se describe como Atribución/Reconocimiento-NoComercial 4.0 Internacional

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