dc.creator | Martits-Chalangari, Katalin | |
dc.creator | Spak, Cedric W. | |
dc.creator | Askar, Medhat | |
dc.creator | Killian, Aaron | |
dc.creator | Fisher, Tammy L. | |
dc.creator | Atillasoy, Ercem | |
dc.creator | Marshall, William L. | |
dc.creator | McNeel, David | |
dc.creator | Miller, Michael D. | |
dc.creator | Mathai, Susan K. | |
dc.creator | Gottlieb, Robert L. | |
dc.date.accessioned | 2022-01-26T14:35:08Z | |
dc.date.available | 2022-01-26T14:35:08Z | |
dc.date.issued | 2021 | |
dc.identifier.uri | https://doi.org/10.1111/ajt.16927 | |
dc.identifier.uri | https://onlinelibrary.wiley.com/doi/10.1111/ajt.16927 | |
dc.identifier.uri | https://repository.tcu.edu/handle/116099117/49912 | |
dc.description.abstract | 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. | |
dc.language.iso | en | en_US |
dc.publisher | Wiley | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.source | American Journal of Transplantation | |
dc.subject | antibiotic: antiviral | |
dc.subject | clinical research/practice | |
dc.subject | heart transplantation/cardiology | |
dc.subject | immunobiology | |
dc.subject | infection and infectious agents-viral: SARS-CoV-2/COVID-19 | |
dc.subject | infectious disease | |
dc.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 | |
dc.type | Article | |
dc.rights.holder | The authors | |
dc.rights.license | https://creativecommons.org/licenses/by-nc-nd/4.0/ | |
local.college | Burnett School of Medicine | |
local.department | Burnett School of Medicine | |
local.persons | Gottleib (SOM) | |