Evidence map›Paper›PMID 36189324›Full record

ArticleFrontiers in immunology2022

Safety of autologous freshly expanded mesenchymal stromal cells for the treatment of graft-versus-host disease.

Elizabeth Stenger, Cynthia R Giver, Amelia Langston, Daniel Kota, Pankoj Kumar Das, Raghavan Chinnadurai, Jacques Galipeau, Edmund K Waller, Muna Qayed

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase I
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02359929 (A Phase I Study of Mesenchymal Stromal Cells for the Treatment of Acute and Chronic Graft Versus Host Disease), which is not on this map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.9field-weighted citation impact, top 8% 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.

NCT02359929 phase1completednot on this map

A Phase I Study of Mesenchymal Stromal Cells for the Treatment of Acute and Chronic Graft Versus Host Disease

TypeinterventionalSponsorEmory UniversityRan2015 to 2021Enrolled11ConditionsGraft Versus Host Disease, Acute Graft Versus Host Disease, Chronic Graft Versus Host DiseaseArmsAutologous mesenchymal stromal cells (MSCs)
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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  9. Stem cell therapies in the clinic.Bioengineering & translational medicine · 2025
    Review
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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

9 authors at 5 institutions in 1 country.

Elizabeth StengerAflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Emory University, Atlanta, GA, United States.
Cynthia R GiverBone Marrow and Stem Cell Transplant Center, Winship Cancer Institute, Emory University, Atlanta, GA, United States.
Amelia LangstonBone Marrow and Stem Cell Transplant Center, Winship Cancer Institute, Emory University, Atlanta, GA, United States.
Daniel KotaBone Marrow and Stem Cell Transplant Center, Winship Cancer Institute, Emory University, Atlanta, GA, United States.
Pankoj Kumar DasBone Marrow and Stem Cell Transplant Center, Winship Cancer Institute, Emory University, Atlanta, GA, United States.
Raghavan ChinnaduraiDepartment of Biomedical Sciences, Mercer University School of Medicine, Savannah, GA, United States.
Jacques GalipeauDepartment of Medicine and Carbone Cancer Center, University of Wisconsin in Madison, Madison, WI, United States.
Edmund K WallerBone Marrow and Stem Cell Transplant Center, Winship Cancer Institute, Emory University, Atlanta, GA, United States.
Muna QayedAflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Emory University, Atlanta, GA, United States.
Emory University · USAflac (United States) · USChildren's Healthcare of Atlanta · USMercer University · USUniversity of Wisconsin Carbone Cancer Center · US

Funding

Atlanta Clinical and Translational Science Institute (ACTSI) RenewalKL2TR000455 · NCATS · EMORY UNIVERSITY · PI STEPHENS, DAVID S · 2012 to 2016
$2.9M
NCATS NIH HHS KL2 TR000455
6 · The paper itself

Abstract

Despite the curative potential of hematopoietic cell transplantation (HCT) for hematologic malignancies, graft-versus-host disease (GVHD) remains a substantial cause of morbidity and mortality, particularly if treatment is refractory. Treatment with additional immunosuppression including steroids often leads to opportunistic infections and organ dysfunction. Novel therapies are greatly needed, specifically ones that lead to responses in treatment-refractory patients and are better tolerated. Mesenchymal stromal cells (MSCs) are non-hematopoietic tolerogenic cells present in normal bone marrow (BM), which can be expanded

Indexed as

Graft vs Host DiseaseHematologic NeoplasmsHematopoietic Stem Cell TransplantationMesenchymal Stem CellsMesenchymal Stem Cell TransplantationAdultHumansSteroidsSteroidsacute graft versus host disease (aGVHD)allogeneic transplant of haematopoietic stem cellschronic graft versus host disease (GVHD)Hematologic malignancyMesechymal stromal cell

Identifiers

PMID36189324
PMCPMC9515357
OpenAlexW4295993323

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.