Evidence map›Paper›PMID 34654057›Full record

ArticleBlood advances2022

Modulating endothelial cells with EGFL7 to diminish aGVHD after allogeneic bone marrow transplantation in mice.

Adrienne M Dorrance, Moutuaata M Moutuou, Chinmayee Goda, Natalie E Sell, Sonu Kalyan, Malith Karunasiri, Rohan Kulkarni, Marie Goulard, Sofia Kolovich, Alexander Rudich and 7 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 51% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

17 authors at 3 institutions in 2 countries.

Adrienne M DorranceThe Ohio State University Comprehensive Cancer Center, Columbus, OH.
Moutuaata M MoutuouDépartement de Microbiologie, Infectiologie et Immunologie, Université de Montréal, Montréal, Canada; and.
Chinmayee GodaThe Ohio State University Comprehensive Cancer Center, Columbus, OH.ORCID 0000-0002-3718-585X
Natalie E SellThe Ohio State University Comprehensive Cancer Center, Columbus, OH.
Sonu KalyanThe Ohio State University Comprehensive Cancer Center, Columbus, OH.
Malith KarunasiriThe Ohio State University Comprehensive Cancer Center, Columbus, OH.
Rohan KulkarniThe Ohio State University Comprehensive Cancer Center, Columbus, OH.ORCID 0000-0002-0660-2075
Marie GoulardThe Ohio State University Comprehensive Cancer Center, Columbus, OH.
Sofia KolovichThe Ohio State University Comprehensive Cancer Center, Columbus, OH.
Alexander RudichThe Ohio State University Comprehensive Cancer Center, Columbus, OH.
Eric NaumannThe Ohio State University Comprehensive Cancer Center, Columbus, OH.
Antoine AckaouiDépartement de Microbiologie, Infectiologie et Immunologie, Université de Montréal, Montréal, Canada; and.
Charles-Etienne BigrasDivision d'Hématologie-Oncologie, Centre de Recherche de l'Hôpital Maisonneuve-Rosemont, Montréal, Canada.
Francis DaudelinDivision d'Hématologie-Oncologie, Centre de Recherche de l'Hôpital Maisonneuve-Rosemont, Montréal, Canada.
Ramiro GarzonThe Ohio State University Comprehensive Cancer Center, Columbus, OH.
Parvathi RanganathanThe Ohio State University Comprehensive Cancer Center, Columbus, OH.
Martin GuimondDépartement de Microbiologie, Infectiologie et Immunologie, Université de Montréal, Montréal, Canada; and.
The Ohio State University · USHôpital Maisonneuve-Rosemont · CAUniversité de Montréal · CA

Funding

Translational Training Grant in Experimental TherapeuticsK12CA133250 · NCI · OHIO STATE UNIVERSITY · PI WILLIAM E. CARSON, Rosa Lapalombella · 2008 to 2026
$15.0M
NCI NIH HHS K12 CA133250
6 · The paper itself

Abstract

Acute graft-versus-host disease (aGVHD) is the second most common cause of death after allogeneic hematopoietic stem cell transplantation (allo-HSCT), underscoring the need for novel therapies. Based on previous work that endothelial cell dysfunction is present in aGVHD and that epidermal growth factor-like domain 7 (EGFL7) plays a significant role in decreasing inflammation by repressing endothelial cell activation and T-cell migration, we hypothesized that increasing EGFL7 levels after allo-HSCT will diminish the severity of aGVHD. Here, we show that treatment with recombinant EGFL7 (rEGFL7) in 2 different murine models of aGVHD decreases aGVHD severity and improves survival in recipient mice after allogeneic transplantation with respect to controls without affecting graft-versus-leukemia effect. Furthermore, we showed that rEGFL7 treatment results in higher thymocytes, T, B, and dendritic cell counts in recipient mice after allo-HSCT. This study constitutes a proof of concept of the ability of rEGFL7 therapy to reduce GHVD severity and mortality after allo-HSCT.

Indexed as

Graft vs Host DiseaseHematopoietic Stem Cell TransplantationAnimalsBone Marrow TransplantationEndothelial CellsMiceTransplantation, Homologous

Identifiers

PMID34654057
PMCPMC9006300
OpenAlexW3206027994

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.