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REDUCED COVID-19 VACCINE RESPONSE IN PATIENT TREATED WITH DUPILUMAB FOR IGG4 RELATED DISEASE.

INTRODUCTION: Dupilumab is a novel anti-interleukin-4 (IL-4) receptor-α monoclonal antibody that targets the signaling pathways of IL-4 and IL-13. There there has been limited data about adequate humoral immune response after vaccination to SARS-CoV-2 in patients on dupilumab. CASE DESCRIPTION: We p...

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Autores principales: Abadeh, A., Lee, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9646421/
http://dx.doi.org/10.1016/j.anai.2022.08.973
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author Abadeh, A.
Lee, J.
author_facet Abadeh, A.
Lee, J.
author_sort Abadeh, A.
collection PubMed
description INTRODUCTION: Dupilumab is a novel anti-interleukin-4 (IL-4) receptor-α monoclonal antibody that targets the signaling pathways of IL-4 and IL-13. There there has been limited data about adequate humoral immune response after vaccination to SARS-CoV-2 in patients on dupilumab. CASE DESCRIPTION: We previously reported the case of a 71-year-old man with IgG4 related-disease (IgG4-RD) that we successfully treated with dupilumab. This patient was followed while his IgG4-RD remained well controlled on dupilumab which he remained on during this pandemic. He received two Pfizer SARS-CoV-2 mRNA vaccinations on March 24 and June 18, 2021. On July 24, 2021, result of SARS-CoV-2 Total-Antibody was non-reactive. As such, a third booster vaccination on November 10, 2021 and timing of holding dupilumab was made to optimize his potential immune response. Dupilumab was held for 1 month prior to his third vaccination and was re-initiated two weeks post-vaccination. On December 3, 2021, his SARS-CoV-2 Total-Antibody was repeated and found to be 2282 U/ml while his SARS-CoV-2-NPROT Total-Antibody was negative, implying immune response through vaccination and not natural exposure. DISCUSSION: To our knowledge, this is the first case report on a patient with IgG4-RD controlled on dupilumab who was found to have adequate vaccine response after his dupilumab was held for 1 month after failing to mount a response to the first two vaccination doses while on therapy. As there is evidence that lower vaccine-specific titers afford less protection against COVID-19, this report highlights this approach as one possible strategy for protecting these individuals who may remain at high risk.
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spelling pubmed-96464212022-11-14 REDUCED COVID-19 VACCINE RESPONSE IN PATIENT TREATED WITH DUPILUMAB FOR IGG4 RELATED DISEASE. Abadeh, A. Lee, J. Ann Allergy Asthma Immunol M358 INTRODUCTION: Dupilumab is a novel anti-interleukin-4 (IL-4) receptor-α monoclonal antibody that targets the signaling pathways of IL-4 and IL-13. There there has been limited data about adequate humoral immune response after vaccination to SARS-CoV-2 in patients on dupilumab. CASE DESCRIPTION: We previously reported the case of a 71-year-old man with IgG4 related-disease (IgG4-RD) that we successfully treated with dupilumab. This patient was followed while his IgG4-RD remained well controlled on dupilumab which he remained on during this pandemic. He received two Pfizer SARS-CoV-2 mRNA vaccinations on March 24 and June 18, 2021. On July 24, 2021, result of SARS-CoV-2 Total-Antibody was non-reactive. As such, a third booster vaccination on November 10, 2021 and timing of holding dupilumab was made to optimize his potential immune response. Dupilumab was held for 1 month prior to his third vaccination and was re-initiated two weeks post-vaccination. On December 3, 2021, his SARS-CoV-2 Total-Antibody was repeated and found to be 2282 U/ml while his SARS-CoV-2-NPROT Total-Antibody was negative, implying immune response through vaccination and not natural exposure. DISCUSSION: To our knowledge, this is the first case report on a patient with IgG4-RD controlled on dupilumab who was found to have adequate vaccine response after his dupilumab was held for 1 month after failing to mount a response to the first two vaccination doses while on therapy. As there is evidence that lower vaccine-specific titers afford less protection against COVID-19, this report highlights this approach as one possible strategy for protecting these individuals who may remain at high risk. Published by Elsevier Inc. 2022-11 2022-11-10 /pmc/articles/PMC9646421/ http://dx.doi.org/10.1016/j.anai.2022.08.973 Text en Copyright © 2022 Published by Elsevier Inc. 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 M358
Abadeh, A.
Lee, J.
REDUCED COVID-19 VACCINE RESPONSE IN PATIENT TREATED WITH DUPILUMAB FOR IGG4 RELATED DISEASE.
title REDUCED COVID-19 VACCINE RESPONSE IN PATIENT TREATED WITH DUPILUMAB FOR IGG4 RELATED DISEASE.
title_full REDUCED COVID-19 VACCINE RESPONSE IN PATIENT TREATED WITH DUPILUMAB FOR IGG4 RELATED DISEASE.
title_fullStr REDUCED COVID-19 VACCINE RESPONSE IN PATIENT TREATED WITH DUPILUMAB FOR IGG4 RELATED DISEASE.
title_full_unstemmed REDUCED COVID-19 VACCINE RESPONSE IN PATIENT TREATED WITH DUPILUMAB FOR IGG4 RELATED DISEASE.
title_short REDUCED COVID-19 VACCINE RESPONSE IN PATIENT TREATED WITH DUPILUMAB FOR IGG4 RELATED DISEASE.
title_sort reduced covid-19 vaccine response in patient treated with dupilumab for igg4 related disease.
topic M358
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9646421/
http://dx.doi.org/10.1016/j.anai.2022.08.973
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