Cargando…
Clinical Management of Patients With B-Cell Depletion Agents to Treat or Prevent Prolonged and Severe SARS-COV-2 Infection: Defining a Treatment Pathway
INTRODUCTION: Immunocompromised patients with B-cell depletion agents are at risk for persistence and/or severe SARS-COV-2 infection. We describe a case series of 21 COVID-19 patients under B cell depletion therapy, mostly treated with a combined therapy based on intravenous remdesevir (RDV) and ste...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9196078/ https://www.ncbi.nlm.nih.gov/pubmed/35711444 http://dx.doi.org/10.3389/fimmu.2022.911339 |
_version_ | 1784727106544992256 |
---|---|
author | D’Abramo, Alessandra Vita, Serena Maffongelli, Gaetano Beccacece, Alessia Agrati, Chiara Cimini, Eleonora Colavita, Francesca Giancola, Maria Letizia Cavasio, Alessandro Nicastri, Emanuele |
author_facet | D’Abramo, Alessandra Vita, Serena Maffongelli, Gaetano Beccacece, Alessia Agrati, Chiara Cimini, Eleonora Colavita, Francesca Giancola, Maria Letizia Cavasio, Alessandro Nicastri, Emanuele |
author_sort | D’Abramo, Alessandra |
collection | PubMed |
description | INTRODUCTION: Immunocompromised patients with B-cell depletion agents are at risk for persistence and/or severe SARS-COV-2 infection. We describe a case series of 21 COVID-19 patients under B cell depletion therapy, mostly treated with a combined therapy based on intravenous remdesevir (RDV) and steroid associated with SARS-CoV-2 monoclonal antibodies against Spike glycoprotein and/or hyper-immune convalescent plasma. METHODS: This is a single-center longitudinal study. We retrospectively enrolled a total number of 21 B-cell depleted consecutive hospitalized patients with COVID-19 at the Lazzaro Spallanzani National Institute for Infectious Diseases, Rome, Italy, from November 2020 to December 2021. Demographic characteristics, medical history, clinical presentation, treatment, adverse drug reactions, and clinical and virological outcome were collected for all patients. In a subgroup, we explore immune T cells activation, T cells specific anti-SARS-COV-2 response, and neutralizing antibodies. RESULTS: Twenty-one inpatients with B-cell depletion and SARS-COV-2 infection were enrolled. A median of 1 B cells/mm(3) was detected. Eighteen patients presented hypogammaglobulinemia. All patients presented interstitial pneumonia treated with intravenous RDV and steroids. Sixteen patients were treated with monoclonal antibodies against SARS-CoV-2 Spike protein, four patients were treated with SARS-CoV-2 hyper-immune convalescent plasma infusion, and three patients received both treatments. A variable kinetic of T cell activation returning to normal levels at Day 30 after immunotherapy infusion was observed. All treated patients recovered. CONCLUSION: In COVID-19 immunosuppressed subjects, it is mandatory to establish a prompt, effective, and combined multi-target therapy including oxygen, antiviral, steroid, and antibody-based therapeutics, tailored to the patient’s clinical needs. |
format | Online Article Text |
id | pubmed-9196078 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91960782022-06-15 Clinical Management of Patients With B-Cell Depletion Agents to Treat or Prevent Prolonged and Severe SARS-COV-2 Infection: Defining a Treatment Pathway D’Abramo, Alessandra Vita, Serena Maffongelli, Gaetano Beccacece, Alessia Agrati, Chiara Cimini, Eleonora Colavita, Francesca Giancola, Maria Letizia Cavasio, Alessandro Nicastri, Emanuele Front Immunol Immunology INTRODUCTION: Immunocompromised patients with B-cell depletion agents are at risk for persistence and/or severe SARS-COV-2 infection. We describe a case series of 21 COVID-19 patients under B cell depletion therapy, mostly treated with a combined therapy based on intravenous remdesevir (RDV) and steroid associated with SARS-CoV-2 monoclonal antibodies against Spike glycoprotein and/or hyper-immune convalescent plasma. METHODS: This is a single-center longitudinal study. We retrospectively enrolled a total number of 21 B-cell depleted consecutive hospitalized patients with COVID-19 at the Lazzaro Spallanzani National Institute for Infectious Diseases, Rome, Italy, from November 2020 to December 2021. Demographic characteristics, medical history, clinical presentation, treatment, adverse drug reactions, and clinical and virological outcome were collected for all patients. In a subgroup, we explore immune T cells activation, T cells specific anti-SARS-COV-2 response, and neutralizing antibodies. RESULTS: Twenty-one inpatients with B-cell depletion and SARS-COV-2 infection were enrolled. A median of 1 B cells/mm(3) was detected. Eighteen patients presented hypogammaglobulinemia. All patients presented interstitial pneumonia treated with intravenous RDV and steroids. Sixteen patients were treated with monoclonal antibodies against SARS-CoV-2 Spike protein, four patients were treated with SARS-CoV-2 hyper-immune convalescent plasma infusion, and three patients received both treatments. A variable kinetic of T cell activation returning to normal levels at Day 30 after immunotherapy infusion was observed. All treated patients recovered. CONCLUSION: In COVID-19 immunosuppressed subjects, it is mandatory to establish a prompt, effective, and combined multi-target therapy including oxygen, antiviral, steroid, and antibody-based therapeutics, tailored to the patient’s clinical needs. Frontiers Media S.A. 2022-05-27 /pmc/articles/PMC9196078/ /pubmed/35711444 http://dx.doi.org/10.3389/fimmu.2022.911339 Text en Copyright © 2022 D’Abramo, Vita, Maffongelli, Beccacece, Agrati, Cimini, Colavita, Giancola, Cavasio, Nicastri and Spallanzani COVID-19 Case Investigation Team https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology D’Abramo, Alessandra Vita, Serena Maffongelli, Gaetano Beccacece, Alessia Agrati, Chiara Cimini, Eleonora Colavita, Francesca Giancola, Maria Letizia Cavasio, Alessandro Nicastri, Emanuele Clinical Management of Patients With B-Cell Depletion Agents to Treat or Prevent Prolonged and Severe SARS-COV-2 Infection: Defining a Treatment Pathway |
title | Clinical Management of Patients With B-Cell Depletion Agents to Treat or Prevent Prolonged and Severe SARS-COV-2 Infection: Defining a Treatment Pathway |
title_full | Clinical Management of Patients With B-Cell Depletion Agents to Treat or Prevent Prolonged and Severe SARS-COV-2 Infection: Defining a Treatment Pathway |
title_fullStr | Clinical Management of Patients With B-Cell Depletion Agents to Treat or Prevent Prolonged and Severe SARS-COV-2 Infection: Defining a Treatment Pathway |
title_full_unstemmed | Clinical Management of Patients With B-Cell Depletion Agents to Treat or Prevent Prolonged and Severe SARS-COV-2 Infection: Defining a Treatment Pathway |
title_short | Clinical Management of Patients With B-Cell Depletion Agents to Treat or Prevent Prolonged and Severe SARS-COV-2 Infection: Defining a Treatment Pathway |
title_sort | clinical management of patients with b-cell depletion agents to treat or prevent prolonged and severe sars-cov-2 infection: defining a treatment pathway |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9196078/ https://www.ncbi.nlm.nih.gov/pubmed/35711444 http://dx.doi.org/10.3389/fimmu.2022.911339 |
work_keys_str_mv | AT dabramoalessandra clinicalmanagementofpatientswithbcelldepletionagentstotreatorpreventprolongedandseveresarscov2infectiondefiningatreatmentpathway AT vitaserena clinicalmanagementofpatientswithbcelldepletionagentstotreatorpreventprolongedandseveresarscov2infectiondefiningatreatmentpathway AT maffongelligaetano clinicalmanagementofpatientswithbcelldepletionagentstotreatorpreventprolongedandseveresarscov2infectiondefiningatreatmentpathway AT beccacecealessia clinicalmanagementofpatientswithbcelldepletionagentstotreatorpreventprolongedandseveresarscov2infectiondefiningatreatmentpathway AT agratichiara clinicalmanagementofpatientswithbcelldepletionagentstotreatorpreventprolongedandseveresarscov2infectiondefiningatreatmentpathway AT ciminieleonora clinicalmanagementofpatientswithbcelldepletionagentstotreatorpreventprolongedandseveresarscov2infectiondefiningatreatmentpathway AT colavitafrancesca clinicalmanagementofpatientswithbcelldepletionagentstotreatorpreventprolongedandseveresarscov2infectiondefiningatreatmentpathway AT giancolamarialetizia clinicalmanagementofpatientswithbcelldepletionagentstotreatorpreventprolongedandseveresarscov2infectiondefiningatreatmentpathway AT cavasioalessandro clinicalmanagementofpatientswithbcelldepletionagentstotreatorpreventprolongedandseveresarscov2infectiondefiningatreatmentpathway AT nicastriemanuele clinicalmanagementofpatientswithbcelldepletionagentstotreatorpreventprolongedandseveresarscov2infectiondefiningatreatmentpathway AT clinicalmanagementofpatientswithbcelldepletionagentstotreatorpreventprolongedandseveresarscov2infectiondefiningatreatmentpathway |