Evidence map›Paper›PMID 32696426›Full record

ArticleStem cell reviews and reports2021

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

Ekaterine Berishvili, Laurent Kaiser, Marie Cohen, Thierry Berney, Hanne Scholz, Yngvar Floisand, Jonas Mattsson

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Stem cell reviews and reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06373809 (Diabetic Foot), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 29% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06373809 early_phase1completednot on this map

Diabetic Foot: Treatment of Chronic Ulcers and Neuropathy With Transplantation of Placenta Derived Stem Cells (PDSC) - A Dose Escalation Safety and Exploratory Efficacy Study

TypeinterventionalSponsorMichael H CarstensRan2021 to 2024Enrolled20ConditionsDiabetic Foot, Diabetic Neuropathies, Diabetic Foot UlcerArmsTransplantation of Placenta Derived Stem Cells
3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 3 countries.

Ekaterine BerishviliCell Isolation and Transplantation Center, University of Geneva School of Medicine, Geneva, Switzerland. ekaterine.berishvili@unige.ch.
Laurent KaiserDivision of Infectious Diseases, Virology Laboratory and Geneva Centre for Emerging Viral Diseases, University of Geneva Hospitals, Geneva, Switzerland.
Marie CohenDepartment of Pediatrics, Gynecology and Obstetrics, University of Geneva School of Medicine, Geneva, Switzerland.
Thierry BerneyCell Isolation and Transplantation Center, University of Geneva School of Medicine, Geneva, Switzerland.
Hanne ScholzDepartment of Transplant Medicine, Department of Cellular Therapy, University of Oslo, Oslo, Norway.
Yngvar FloisandDepartment of Hematology, Oslo University Hospital, Oslo, Norway.
Jonas MattssonGloria and Seymour Epstein Chair in Cell Therapy and Transplantation, University of Toronto, Toronto, Ontario, Canada.
University of Geneva · CHOslo University Hospital · NOUniversity of Oslo · NOUniversity of Toronto · CA

Funding

Horizon 2020 Framework Programme 874700Juvenile Diabetes Research Foundation United States of America 3-SRA-2020-926-S-BShota Rustaveli National Science Foundation FR-19-19760
6 · The paper itself

Abstract

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.

Indexed as

Cell- and Tissue-Based TherapyAntiviral AgentsClinical Trials as TopicCOVID-19Cytokine Release SyndromeCytokinesFemaleHumansLungPlacentaPneumoniaPregnancyAntiviral AgentsCytokines

Identifiers

PMID32696426
PMCPMC7372209
OpenAlexW3043887763

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.