Cargando…

ALVR109, an off-the-shelf partially HLA matched SARS-CoV-2–specific T cell therapy, to treat refractory severe COVID-19 pneumonia in a heart transplant patient: Case report

An unvaccinated adult male heart transplant recipient patient with recalcitrant COVID-19 due to SARS-CoV-2 delta variant with rising nasopharyngeal quantitative viral load was successfully treated with ALVR109, an off-the-shelf SARS-CoV-2–specific T cell therapy. Background immunosuppression include...

Descripción completa

Detalles Bibliográficos
Autores principales: Martits-Chalangari, Katalin, Spak, Cedric W., Askar, Medhat, Killian, Aaron, Fisher, Tammy L., Atillasoy, Ercem, Marshall, William L., McNeel, David, Miller, Michael D., Mathai, Susan K., Gottlieb, Robert L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Transplantation & American Society of Transplant Surgeons. Published by Elsevier Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303326/
https://www.ncbi.nlm.nih.gov/pubmed/34910857
http://dx.doi.org/10.1111/ajt.16927
_version_ 1784751836739141632
author Martits-Chalangari, Katalin
Spak, Cedric W.
Askar, Medhat
Killian, Aaron
Fisher, Tammy L.
Atillasoy, Ercem
Marshall, William L.
McNeel, David
Miller, Michael D.
Mathai, Susan K.
Gottlieb, Robert L.
author_facet Martits-Chalangari, Katalin
Spak, Cedric W.
Askar, Medhat
Killian, Aaron
Fisher, Tammy L.
Atillasoy, Ercem
Marshall, William L.
McNeel, David
Miller, Michael D.
Mathai, Susan K.
Gottlieb, Robert L.
author_sort Martits-Chalangari, Katalin
collection PubMed
description An unvaccinated adult male heart transplant recipient patient with recalcitrant COVID-19 due to SARS-CoV-2 delta variant with rising nasopharyngeal quantitative viral load was successfully treated with ALVR109, an off-the-shelf SARS-CoV-2–specific T cell therapy. Background immunosuppression included 0.1 mg/kg prednisone, tacrolimus, and mycophenolate mofetil 1 gm twice daily for historical antibody-mediated rejection. Prior therapies included remdesivir, corticosteroids, and tocilizumab, with requirement for high-flow nasal oxygen. Lack of clinical improvement and acutely rising nasopharyngeal viral RNA more than 3 weeks into illness prompted the request of ALVR109 through an emergency IND. The day following the first ALVR109 infusion, the patient’s nasopharyngeal SARS-CoV-2 RNA declined from 7.43 to 5.02 log(10) RNA copies/ml. On post-infusion day 4, the patient transitioned to low-flow oxygen. Two subsequent infusions of ALVR109 were administered 10 and 26 days after the first; nasopharyngeal SARS-CoV-2 RNA became undetectable on Day 11, and he was discharged the following day on low-flow oxygen 5 weeks after the initial diagnosis of COVID-19. The clinical and virologic improvements observed in this patient following administration of ALVR109 suggest a potential benefit that warrants further exploration in clinical trials.
format Online
Article
Text
id pubmed-9303326
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher American Society of Transplantation & American Society of Transplant Surgeons. Published by Elsevier Inc.
record_format MEDLINE/PubMed
spelling pubmed-93033262022-07-22 ALVR109, an off-the-shelf partially HLA matched SARS-CoV-2–specific T cell therapy, to treat refractory severe COVID-19 pneumonia in a heart transplant patient: Case report Martits-Chalangari, Katalin Spak, Cedric W. Askar, Medhat Killian, Aaron Fisher, Tammy L. Atillasoy, Ercem Marshall, William L. McNeel, David Miller, Michael D. Mathai, Susan K. Gottlieb, Robert L. Am J Transplant Case Report An unvaccinated adult male heart transplant recipient patient with recalcitrant COVID-19 due to SARS-CoV-2 delta variant with rising nasopharyngeal quantitative viral load was successfully treated with ALVR109, an off-the-shelf SARS-CoV-2–specific T cell therapy. Background immunosuppression included 0.1 mg/kg prednisone, tacrolimus, and mycophenolate mofetil 1 gm twice daily for historical antibody-mediated rejection. Prior therapies included remdesivir, corticosteroids, and tocilizumab, with requirement for high-flow nasal oxygen. Lack of clinical improvement and acutely rising nasopharyngeal viral RNA more than 3 weeks into illness prompted the request of ALVR109 through an emergency IND. The day following the first ALVR109 infusion, the patient’s nasopharyngeal SARS-CoV-2 RNA declined from 7.43 to 5.02 log(10) RNA copies/ml. On post-infusion day 4, the patient transitioned to low-flow oxygen. Two subsequent infusions of ALVR109 were administered 10 and 26 days after the first; nasopharyngeal SARS-CoV-2 RNA became undetectable on Day 11, and he was discharged the following day on low-flow oxygen 5 weeks after the initial diagnosis of COVID-19. The clinical and virologic improvements observed in this patient following administration of ALVR109 suggest a potential benefit that warrants further exploration in clinical trials. American Society of Transplantation & American Society of Transplant Surgeons. Published by Elsevier Inc. 2022-04 2022-12-30 /pmc/articles/PMC9303326/ /pubmed/34910857 http://dx.doi.org/10.1111/ajt.16927 Text en Copyright © 2022 American Society of Transplantation & American Society of Transplant Surgeons. Published by Elsevier Inc. All rights reserved. Published by Elsevier B.V. All rights reserved. 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 Report
Martits-Chalangari, Katalin
Spak, Cedric W.
Askar, Medhat
Killian, Aaron
Fisher, Tammy L.
Atillasoy, Ercem
Marshall, William L.
McNeel, David
Miller, Michael D.
Mathai, Susan K.
Gottlieb, Robert L.
ALVR109, an off-the-shelf partially HLA matched SARS-CoV-2–specific T cell therapy, to treat refractory severe COVID-19 pneumonia in a heart transplant patient: Case report
title ALVR109, an off-the-shelf partially HLA matched SARS-CoV-2–specific T cell therapy, to treat refractory severe COVID-19 pneumonia in a heart transplant patient: Case report
title_full ALVR109, an off-the-shelf partially HLA matched SARS-CoV-2–specific T cell therapy, to treat refractory severe COVID-19 pneumonia in a heart transplant patient: Case report
title_fullStr ALVR109, an off-the-shelf partially HLA matched SARS-CoV-2–specific T cell therapy, to treat refractory severe COVID-19 pneumonia in a heart transplant patient: Case report
title_full_unstemmed ALVR109, an off-the-shelf partially HLA matched SARS-CoV-2–specific T cell therapy, to treat refractory severe COVID-19 pneumonia in a heart transplant patient: Case report
title_short ALVR109, an off-the-shelf partially HLA matched SARS-CoV-2–specific T cell therapy, to treat refractory severe COVID-19 pneumonia in a heart transplant patient: Case report
title_sort alvr109, an off-the-shelf partially hla matched sars-cov-2–specific t cell therapy, to treat refractory severe covid-19 pneumonia in a heart transplant patient: case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303326/
https://www.ncbi.nlm.nih.gov/pubmed/34910857
http://dx.doi.org/10.1111/ajt.16927
work_keys_str_mv AT martitschalangarikatalin alvr109anofftheshelfpartiallyhlamatchedsarscov2specifictcelltherapytotreatrefractoryseverecovid19pneumoniainahearttransplantpatientcasereport
AT spakcedricw alvr109anofftheshelfpartiallyhlamatchedsarscov2specifictcelltherapytotreatrefractoryseverecovid19pneumoniainahearttransplantpatientcasereport
AT askarmedhat alvr109anofftheshelfpartiallyhlamatchedsarscov2specifictcelltherapytotreatrefractoryseverecovid19pneumoniainahearttransplantpatientcasereport
AT killianaaron alvr109anofftheshelfpartiallyhlamatchedsarscov2specifictcelltherapytotreatrefractoryseverecovid19pneumoniainahearttransplantpatientcasereport
AT fishertammyl alvr109anofftheshelfpartiallyhlamatchedsarscov2specifictcelltherapytotreatrefractoryseverecovid19pneumoniainahearttransplantpatientcasereport
AT atillasoyercem alvr109anofftheshelfpartiallyhlamatchedsarscov2specifictcelltherapytotreatrefractoryseverecovid19pneumoniainahearttransplantpatientcasereport
AT marshallwilliaml alvr109anofftheshelfpartiallyhlamatchedsarscov2specifictcelltherapytotreatrefractoryseverecovid19pneumoniainahearttransplantpatientcasereport
AT mcneeldavid alvr109anofftheshelfpartiallyhlamatchedsarscov2specifictcelltherapytotreatrefractoryseverecovid19pneumoniainahearttransplantpatientcasereport
AT millermichaeld alvr109anofftheshelfpartiallyhlamatchedsarscov2specifictcelltherapytotreatrefractoryseverecovid19pneumoniainahearttransplantpatientcasereport
AT mathaisusank alvr109anofftheshelfpartiallyhlamatchedsarscov2specifictcelltherapytotreatrefractoryseverecovid19pneumoniainahearttransplantpatientcasereport
AT gottliebrobertl alvr109anofftheshelfpartiallyhlamatchedsarscov2specifictcelltherapytotreatrefractoryseverecovid19pneumoniainahearttransplantpatientcasereport