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

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 experience...

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Autores principales: Nguyen, Hanna, Salkeld, Jo, Agarwal, Sangita, Goodman, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Author(s). Published by Elsevier Ltd on behalf of British Infection Association. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373583/
https://www.ncbi.nlm.nih.gov/pubmed/34426799
http://dx.doi.org/10.1016/j.clinpr.2021.100089
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author Nguyen, Hanna
Salkeld, Jo
Agarwal, Sangita
Goodman, Anna
author_facet Nguyen, Hanna
Salkeld, Jo
Agarwal, Sangita
Goodman, Anna
author_sort Nguyen, Hanna
collection PubMed
description 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.
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spelling pubmed-83735832021-08-19 Compassionate use of REGN-COV2 in the treatment of COVID-19 in a patient with impaired humoral immunity Nguyen, Hanna Salkeld, Jo Agarwal, Sangita Goodman, Anna Clin Infect Pract Case Reports and Series 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. The Author(s). Published by Elsevier Ltd on behalf of British Infection Association. 2021-11 2021-08-19 /pmc/articles/PMC8373583/ /pubmed/34426799 http://dx.doi.org/10.1016/j.clinpr.2021.100089 Text en © 2021 The Author(s) Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Case Reports and Series
Nguyen, Hanna
Salkeld, Jo
Agarwal, Sangita
Goodman, Anna
Compassionate use of REGN-COV2 in the treatment of COVID-19 in a patient with impaired humoral immunity
title Compassionate use of REGN-COV2 in the treatment of COVID-19 in a patient with impaired humoral immunity
title_full Compassionate use of REGN-COV2 in the treatment of COVID-19 in a patient with impaired humoral immunity
title_fullStr Compassionate use of REGN-COV2 in the treatment of COVID-19 in a patient with impaired humoral immunity
title_full_unstemmed Compassionate use of REGN-COV2 in the treatment of COVID-19 in a patient with impaired humoral immunity
title_short Compassionate use of REGN-COV2 in the treatment of COVID-19 in a patient with impaired humoral immunity
title_sort compassionate use of regn-cov2 in the treatment of covid-19 in a patient with impaired humoral immunity
topic Case Reports and Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373583/
https://www.ncbi.nlm.nih.gov/pubmed/34426799
http://dx.doi.org/10.1016/j.clinpr.2021.100089
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