Evidence map›Paper›PMID 25079358›Full record

ArticleBlood2014

Absence of STAT1 in donor-derived plasmacytoid dendritic cells results in increased STAT3 and attenuates murine GVHD.

Christian M Capitini, Nicole M Nasholm, Christopher D Chien, Shannon M Larabee, Haiying Qin, Young K Song, Peter J Klover, Lothar Hennighausen, Javed Khan, Terry J Fry

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Plasmacytoid dendritic cells in the eye.Progress in retinal and eye research · 2021
    Review
  4. Janus Kinase Inhibitors and Cell Therapy.Frontiers in immunology · 2021
    Review
  5. Combining Immunocytokine andFrontiers in immunology · 2021
    Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. STAT3 Expression in Host Myeloid Cells Controls Graft-versus-Host Disease Severity.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2017
    Article
  11. Article
  12. Article
  13. Review
  14. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

Christian M CapitiniDepartment of Pediatrics and Carbone Cancer Center, University of Wisconsin School of Medicine and Public Health, Madison, WI;ORCID http://orcid.org/0000-0002-2276-6731
Nicole M NasholmPediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, and.
Christopher D ChienPediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, and.
Shannon M LarabeePediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, and.
Haiying QinPediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, and.
Young K SongPediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, and.
Peter J KloverLaboratory of Genetics and Physiology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD.
Lothar HennighausenLaboratory of Genetics and Physiology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD.
Javed KhanPediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, and.
Terry J FryPediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, and.
Cancer Institute (WIA) · INNational Institutes of Health · USUniversity of Wisconsin Carbone Cancer Center · US

Funding

Genetic Approaches To Understanding Organ Development and FunctionZIADK061000 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI HENNIGHAUSEN, LOTHAR · 2009 to 2025
$24.7M
Optimizing the graft versus leukemia effect for pediatric ALLZIABC011295 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI FRY, TERRY · 2010 to 2018
$4.8M
Inhibiting STAT1 as a novel graft-versus-host/graft-versus-leukemia therapyK08CA174750 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI CAPITINI, CHRISTIAN · 2014 to 2017
$715k
Intramural NIH HHSNCI NIH HHS K08 CA174750
6 · The paper itself

Abstract

Selective targeting of non-T cells, including antigen-presenting cells (APCs), is a potential strategy to prevent graft-versus-host-disease (GVHD) but to maintain graft-versus-tumor (GVT) effects. Because type I and II interferons signal through signal transducer and activator of transcription-1 (STAT1), and contribute to activation of APCs after allogeneic bone marrow transplant (alloBMT), we examined whether the absence of STAT1 in donor APCs could prevent GVHD while preserving immune competence. Transplantation of STAT1(-/-) bone marrow (BM) prevented GVHD induced by STAT1(+/+) T cells, leading to expansion of B220(+) cells and regulatory T cells. STAT1(-/-) BM also preserved GVT activity and enhanced overall survival of tumor-challenged mice in the setting of GVHD. Furthermore, recipients of allogeneic STAT1(-/-) BM demonstrated increased CD9(-)Siglec H(hi) plasmacytoid dendritic cells (pDCs), and depletion of pDCs after STAT1(-/-) BM transplantation prevented GVHD resistance. STAT1(-/-) pDCs were found to produce decreased free radicals, IFNα, and interleukin (IL)-12, and increased IL-10. Additionally, STAT1(-/-) pDCs that were isolated after alloBMT showed increased gene expression of S100A8 and S100A9, and transplantation of S100A9(-/-) BM reduced GVHD-free survival. Finally, elevated STAT3 was found in STAT1(-/-) pDCs isolated after alloBMT. We conclude that interfering with interferon signaling in APCs such as pDCs provides a novel approach to regulate the GVHD/GVT axis.

Indexed as

AllograftsAnimalsBone Marrow TransplantationCalgranulin ACalgranulin BDendritic CellsFemaleGene ExpressionGraft vs Host DiseaseMaleMiceMice, 129 StrainMice, Inbred C3HMice, Inbred C57BLMice, KnockoutMice, TransgenicCalgranulin ACalgranulin BS100a8 protein, mouseS100A9 protein, mouseStat1 protein, mouseSTAT1 Transcription FactorStat3 protein, mouseSTAT3 Transcription Factor

Identifiers

PMID25079358
PMCPMC4168352
OpenAlexW2038706799

What OpenQuestion holds

Textmetadata
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.