Evidence map›Paper›PMID 37924979›Full record

ArticleTransplantation and cellular therapy2024

Exopolysaccharide-Treated Dendritic Cells Effectively Ameliorate Acute Graft-versus-Host Disease.

Olga Kalinina, Lisa M Minter, Anne I Sperling, Maile K Hollinger, Phong Le, Barbara A Osborne, Shubin Zhang, Patrick Stiff, Katherine L Knight

Open access · greenAbstract read
In one paragraph

Article in Transplantation and cellular therapy, 2024. 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
1.2field-weighted citation impact, top 18% 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, 4 citations in OpenAlex.

  1. Article
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 4 institutions in 1 country.

Olga KalininaDepartment of Microbiology and Immunology, Stritch School of Medicine, Loyola University Chicago, Maywood, Illinois.
Lisa M MinterDepartment of Veterinary & Animal Sciences, University of Massachusetts, Amherst, Massachusetts.
Anne I SperlingDepartment of Medicine, Pulmonary Division, and Carter Center for Immunology, University of Virginia, Charlottesville, Virginia.
Maile K HollingerCommittee on Immunology, University of Chicago, Chicago, Illinois.
Phong LeDepartment of Microbiology and Immunology, Stritch School of Medicine, Loyola University Chicago, Maywood, Illinois.
Barbara A OsborneDepartment of Veterinary & Animal Sciences, University of Massachusetts, Amherst, Massachusetts; HasenTech, LLC, Leverett, Massachusetts.
Shubin ZhangDepartment of Microbiology and Immunology, Stritch School of Medicine, Loyola University Chicago, Maywood, Illinois.
Patrick StiffHematology-Oncology Division, Department of Medicine, Stritch School of Medicine, Loyola University Chicago, Maywood, Illinois.
Katherine L KnightDepartment of Microbiology and Immunology, Stritch School of Medicine, Loyola University Chicago, Maywood, Illinois; HasenTech, LLC, Leverett, Massachusetts. Electronic address: kknight@luc.edu.
Loyola University Chicago · USUniversity of Massachusetts Amherst · USCarter Center · USUniversity of Chicago · US

Funding

Commensal Exopolysaccharide Protection from InflammationR01AI110586 · NIAID · LOYOLA UNIVERSITY CHICAGO · PI KNIGHT, KATHERINE L. · 2015 to 2019
$1.9M
Protection from enteric pathogens by beneficial microbesR21AI098187 · NIAID · LOYOLA UNIVERSITY CHICAGO · PI KNIGHT, KATHERINE L. · 2012 to 2013
$401k
Prevention of GVHD by a probiotic exopolysaccharide.R41AI155281 · NIAID · HASENTECH, INC. · PI KNIGHT, KATHERINE L., OSBORNE, BARBARA A · 2020 to 2020
$300k
NIAID NIH HHS R01 AI110586NIAID NIH HHS R21 AI098187NIAID NIH HHS R41 AI155281
6 · The paper itself

Abstract

Graft-versus-host disease (GVHD) is a primary and often lethal complication of allogenic hematopoietic stem cell transplantation (HSCT). Prophylactic regimens for GVHD are given as standard pretransplantation therapy; however, up to 50% of these patients develop acute GVHD (aGVHD) and require additional immunosuppressive intervention. Using a mouse GVHD model, we previously showed that injecting mice with exopolysaccharide (EPS) from Bacillus subtilis prior to GVHD induction significantly increased 80-day survival after transplantation of complete allogeneic major histocompatibility complex-mismatched cells. To ask whether EPS might also inhibit GVHD in humans, we used humanized NSG-HLA-A2 mice and induced GVHD by i.v. injection of A2

Indexed as

Graft vs Host DiseaseHLA-A2 AntigenAnimalsDendritic CellsDisease Models, AnimalHumansLeukocytes, MononuclearTransplantation, HomologousHLA-A2 AntigenDendritic cellsExopolysaccharideGVHDHumanized mouse

Identifiers

PMID37924979
PMCPMC12306621
OpenAlexW4388248427

What OpenQuestion holds

Textmetadata
LicenceTDM
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.