Evidence map›Paper›PMID 32250356›Full record

ArticleJournal of visualized experiments : JoVE2020

Bone Marrow Transplantation Platform to Investigate the Role of Dendritic Cells in Graft-versus-Host Disease.

Hung D Nguyen, Phung Thanh Huong, Krystal Hossack, Sanjeev Gurshaney, Kevin Ezhakunnel, Thien-Huong Huynh, Anamaria Morales Alvarez, Nhat-Tu Le, Hung N Luu

Open access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2020. 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
–field-weighted citation impact, top 97% 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, 1 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 2 countries.

Hung D Nguyen *Cancer Division, Burnett School of Biomedical Sciences, University of Central Florida; hung.nguyen@ucf.edu.
Phung Thanh Huong *Department of Biochemistry, Hanoi University of Pharmacy.
Krystal HossackCancer Division, Burnett School of Biomedical Sciences, University of Central Florida.
Sanjeev GurshaneyCancer Division, Burnett School of Biomedical Sciences, University of Central Florida.
Kevin EzhakunnelCancer Division, Burnett School of Biomedical Sciences, University of Central Florida.
Thien-Huong HuynhCancer Division, Burnett School of Biomedical Sciences, University of Central Florida.
Anamaria Morales AlvarezCancer Division, Burnett School of Biomedical Sciences, University of Central Florida.
Nhat-Tu LeCenter for Cardiovascular Regeneration, Department of Cardiovascular Sciences, Houston Methodist Research Institute.
Hung N LuuDepartment of Epidemiology, University of Pittsburgh Graduate School of Public Health; Division of Cancer Control and Population Sciences, University of Pittsburgh Medical Center, Hillman Cancer Center.
University of Central Florida · USHanoi University of Pharmacy · VNHouston Methodist · USUPMC Hillman Cancer Center · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JOHN C. BYRD · 1988 to 2026
$158.0M
Regional Center of Research Excellence in Cancer and Other Non-Communicable Disease Epidemiology and Prevention in VietnamP20CA210300 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SHU, XIAO-OU · 2016 to 2017
$549k
NCI NIH HHS P20 CA210300NCI NIH HHS P30 CA047904
6 · The paper itself

Abstract

Allogeneic bone marrow transplantation (BMT) is an effective therapy for hematological malignancies due to the graft-versus-leukemia (GVL) effect to eradicate tumors. However, its application is limited by the development of graft-versus-host disease (GVHD), a major complication of BMT. GVHD is evoked when T-cells in the donor grafts recognizealloantigen expressed by recipient cells and mount unwanted immunological attacks against recipient healthy tissues. Thus, traditional therapies are designed to suppress donor T-cell alloreactivity. However, these approaches substantially impair the GVL effect so that the recipient's survival is not improved. Understanding the effects of therapeutic approaches on BMT, GVL, and GVHD, is thus essential. Due to the antigen-presenting and cytokine-secreting capacities to stimulate donor T-cells, recipient dendritic cells (DCs) play a significant role in the induction of GVHD. Therefore, targeting recipient DCs becomes a potential approach for controlling GVHD. This work provides a description of a novel BMT platform to investigate how host DCs regulate GVH and GVL responses after transplantation. Also presented is an effective BMT model to study the biology of GVHD and GVL after transplantation.

Indexed as

Bone Marrow TransplantationAnimalsDendritic CellsGraft vs Host DiseaseHumansT-Lymphocytes

Identifiers

PMID32250356
PMCPMC11537245
OpenAlexW3011560761

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.