Cargando…

Treatment of COVID-19 Pneumonia: the Case for Placenta-derived Cell Therapy

Nearly 500’000 fatalities due to COVID-19 have been reported globally and the death toll is still rising. Most deaths are due to acute respiratory distress syndrome (ARDS), as a result of an excessive immune response and a cytokine storm elicited by severe SARS-CoV-2 lung infection, rather than by a...

Descripción completa

Detalles Bibliográficos
Autores principales: Berishvili, Ekaterine, Kaiser, Laurent, Cohen, Marie, Berney, Thierry, Scholz, Hanne, Floisand, Yngvar, Mattsson, Jonas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7372209/
https://www.ncbi.nlm.nih.gov/pubmed/32696426
http://dx.doi.org/10.1007/s12015-020-10004-x
_version_ 1783561265545740288
author Berishvili, Ekaterine
Kaiser, Laurent
Cohen, Marie
Berney, Thierry
Scholz, Hanne
Floisand, Yngvar
Mattsson, Jonas
author_facet Berishvili, Ekaterine
Kaiser, Laurent
Cohen, Marie
Berney, Thierry
Scholz, Hanne
Floisand, Yngvar
Mattsson, Jonas
author_sort Berishvili, Ekaterine
collection PubMed
description Nearly 500’000 fatalities due to COVID-19 have been reported globally and the death toll is still rising. Most deaths are due to acute respiratory distress syndrome (ARDS), as a result of an excessive immune response and a cytokine storm elicited by severe SARS-CoV-2 lung infection, rather than by a direct cytopathic effect of the virus. In the most severe forms of the disease therapies should aim primarily at dampening the uncontrolled inflammatory/immune response responsible for most fatalities. Pharmacological agents - antiviral and anti-inflammatory molecules - have not been able so far to achieve compelling results for the control of severe COVID-19 pneumonia. Cells derived from the placenta and/or fetal membranes, in particular amniotic epithelial cells (AEC) and decidual stromal cells (DSC), have established, well-characterized, potent anti-inflammatory and immune-modulatory properties that make them attractive candidates for a cell-based therapy of COVID19 pneumonia. Placenta-derived cells are easy to procure from a perennial source and pose minimal ethical issues for their utilization. In view of the existing clinical evidence for the innocuousness and efficiency of systemic administration of DSCs or AECs in similar conditions, we advocate for the initiation of clinical trials using this strategy in the treatment of severe COVID-19 disease.
format Online
Article
Text
id pubmed-7372209
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-73722092020-07-21 Treatment of COVID-19 Pneumonia: the Case for Placenta-derived Cell Therapy Berishvili, Ekaterine Kaiser, Laurent Cohen, Marie Berney, Thierry Scholz, Hanne Floisand, Yngvar Mattsson, Jonas Stem Cell Rev Rep Article Nearly 500’000 fatalities due to COVID-19 have been reported globally and the death toll is still rising. Most deaths are due to acute respiratory distress syndrome (ARDS), as a result of an excessive immune response and a cytokine storm elicited by severe SARS-CoV-2 lung infection, rather than by a direct cytopathic effect of the virus. In the most severe forms of the disease therapies should aim primarily at dampening the uncontrolled inflammatory/immune response responsible for most fatalities. Pharmacological agents - antiviral and anti-inflammatory molecules - have not been able so far to achieve compelling results for the control of severe COVID-19 pneumonia. Cells derived from the placenta and/or fetal membranes, in particular amniotic epithelial cells (AEC) and decidual stromal cells (DSC), have established, well-characterized, potent anti-inflammatory and immune-modulatory properties that make them attractive candidates for a cell-based therapy of COVID19 pneumonia. Placenta-derived cells are easy to procure from a perennial source and pose minimal ethical issues for their utilization. In view of the existing clinical evidence for the innocuousness and efficiency of systemic administration of DSCs or AECs in similar conditions, we advocate for the initiation of clinical trials using this strategy in the treatment of severe COVID-19 disease. Springer US 2020-07-21 2021 /pmc/articles/PMC7372209/ /pubmed/32696426 http://dx.doi.org/10.1007/s12015-020-10004-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Berishvili, Ekaterine
Kaiser, Laurent
Cohen, Marie
Berney, Thierry
Scholz, Hanne
Floisand, Yngvar
Mattsson, Jonas
Treatment of COVID-19 Pneumonia: the Case for Placenta-derived Cell Therapy
title Treatment of COVID-19 Pneumonia: the Case for Placenta-derived Cell Therapy
title_full Treatment of COVID-19 Pneumonia: the Case for Placenta-derived Cell Therapy
title_fullStr Treatment of COVID-19 Pneumonia: the Case for Placenta-derived Cell Therapy
title_full_unstemmed Treatment of COVID-19 Pneumonia: the Case for Placenta-derived Cell Therapy
title_short Treatment of COVID-19 Pneumonia: the Case for Placenta-derived Cell Therapy
title_sort treatment of covid-19 pneumonia: the case for placenta-derived cell therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7372209/
https://www.ncbi.nlm.nih.gov/pubmed/32696426
http://dx.doi.org/10.1007/s12015-020-10004-x
work_keys_str_mv AT berishviliekaterine treatmentofcovid19pneumoniathecaseforplacentaderivedcelltherapy
AT kaiserlaurent treatmentofcovid19pneumoniathecaseforplacentaderivedcelltherapy
AT cohenmarie treatmentofcovid19pneumoniathecaseforplacentaderivedcelltherapy
AT berneythierry treatmentofcovid19pneumoniathecaseforplacentaderivedcelltherapy
AT scholzhanne treatmentofcovid19pneumoniathecaseforplacentaderivedcelltherapy
AT floisandyngvar treatmentofcovid19pneumoniathecaseforplacentaderivedcelltherapy
AT mattssonjonas treatmentofcovid19pneumoniathecaseforplacentaderivedcelltherapy