دورية أكاديمية

Compassionate use of REGN-COV2 in the treatment of COVID-19 in a patient with impaired humoral immunity

التفاصيل البيبلوغرافية
العنوان: Compassionate use of REGN-COV2 in the treatment of COVID-19 in a patient with impaired humoral immunity
المؤلفون: Hanna Nguyen, Jo Salkeld, Sangita Agarwal, Anna Goodman
المصدر: Clinical Infection in Practice, Vol 12, Iss , Pp 100089- (2021)
بيانات النشر: Elsevier, 2021.
سنة النشر: 2021
المجموعة: LCC:Infectious and parasitic diseases
مصطلحات موضوعية: SARS-CoV2, COVID-19, Agammaglobulinemia, REGN-COV2, Remdesivir, Infectious and parasitic diseases, RC109-216
الوصف: Background: The role of antibodies in coronavirus disease 2019 (COVID-19) in patients with X-linked agammaglobulinaemia (XLA) has yet to be characterised and clinical courses observed in this cohort of patients have been heterogeneous. Whilst some exhibit spontaneous recovery, others have experienced a more protracted disease length. Previous reports have described successful use of convalescent plasma, however there is a paucity of information around the use of the REGN-COV2 antibody cocktail in these patients. Case report: A patient with XLA was admitted to hospital with COVID-19 and remained persistently symptomatic with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) swab positivity despite treatment with Remdesivir and dexamethasone. Attempts at modulating the immune response with anakinra were unsuccessful. Consent for compassionate use of REGN-COV2 was obtained with administration taking place on day 87 of his illness. This was followed by a period of convalescence and SARS-CoV-2 nasopharyngeal swab negativity. As a consequence of prolonged immunosuppression, the patient developed pneumocystis pneumonia. Conclusion: This case highlights the role of antibodies in clearing SARS-CoV-2 in a hypogammaglobulinaemic host and demonstrates the consequences of prolonged immunosuppression and delayed treatment. We propose that this may be of particular significance given the capacity of SARS-CoV-2 to develop advantageous mutations in a chronically infected host.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2590-1702
Relation: http://www.sciencedirect.com/science/article/pii/S2590170221000261; https://doaj.org/toc/2590-1702
DOI: 10.1016/j.clinpr.2021.100089
URL الوصول: https://doaj.org/article/eafc09616b3c478081696222d1ddd260
رقم الأكسشن: edsdoj.fc09616b3c478081696222d1ddd260
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:25901702
DOI:10.1016/j.clinpr.2021.100089