Evidence map›Paper›PMID 24695850›Full record

ArticleBlood2014

Siglec-G-CD24 axis controls the severity of graft-versus-host disease in mice.

Tomomi Toubai, Guoqing Hou, Nathan Mathewson, Chen Liu, Ying Wang, Katherine Oravecz-Wilson, Emily Cummings, Corinne Rossi, Rebecca Evers, Yaping Sun and 6 more

Registry-linked trialOpen 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. It is linked to trial NCT02663622 (A Phase II Trial of CD24Fc for Prevention of Acute Graft-versus-Host Disease Following Myeloablative Allogeneic Hematopoietic Stem Cell Transplant), which is not on this map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
3.6field-weighted citation impact, top 7% 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.

NCT02663622 phase2completednot on this mapstarted 2016, after this paper: background citation

A Phase II Trial of CD24Fc for Prevention of Acute Graft-versus-Host Disease Following Myeloablative Allogeneic Hematopoietic Stem Cell Transplant

TypeinterventionalSponsorOncoimmune, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)Ran2016 to 2021Enrolled44ConditionsGraft Versus Host Disease, Hematopoietic Stem Cell Transplantation, LeukemiaArmsEfprezimod alfa, Methotrexate, Tacrolimus, Placebo
3 · Its place in the literature

Who cites it

64 citing papers in PubMed, 93 citations in OpenAlex.

  1. Trial
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  5. Article
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  12. Siglec-G Suppresses CD8Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. The new progress in cancer immunotherapy.Clinical and experimental medicine · 2023
    Review
  18. Article
  19. Activation of immune signals during organ transplantation.Signal transduction and targeted therapy · 2023
    Review
  20. Emerging phagocytosis checkpoints in cancer immunotherapy.Signal transduction and targeted therapy · 2023
    Review

4 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 5 institutions in 1 country.

Tomomi ToubaiDepartment of Internal Medicine, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI;
Guoqing HouDepartment of Internal Medicine, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI;
Nathan MathewsonDepartment of Internal Medicine, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI;
Chen LiuDepartment of Pathology, University of Florida College of Medicine, Gainesville, FL;
Ying WangDepartment of Internal Medicine, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI;
Katherine Oravecz-WilsonDepartment of Internal Medicine, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI;
Emily CummingsDepartment of Internal Medicine, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI;
Corinne RossiDepartment of Internal Medicine, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI;
Rebecca EversDepartment of Internal Medicine, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI;
Yaping SunDepartment of Internal Medicine, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI;
Julia WuDepartment of Internal Medicine, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI;
Sung Won ChoiDepartment of Pediatrics and Communicable Diseases, University of Michigan Medical School, Ann Arbor, MI;
Dexing FangOncoImmune, Inc., Rockville, MD; and.
Pan ZhengCenter for Cancer and Immunology Research, Children's National Medical Center, Washington, DC.
Yang LiuCenter for Cancer and Immunology Research, Children's National Medical Center, Washington, DC.
Pavan ReddyDepartment of Internal Medicine, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI;
University of Michigan–Ann Arbor · USMichigan Center for Translational Pathology · USChildren's National · USOncoImmune (United States) · USUniversity of Florida · US

Funding

Targeting antigen presentation to enhance GVL responses after Bone Marrow TransplR01HL090775 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI REDDY, PAVAN · 2008 to 2016
$3.4M
Targeting Novel DAMP mediated signaling pathways to mitigate GVHDR01CA217156 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI REDDY, PAVAN · 2017 to 2022
$1.9M
Role of noncoding RNA in Regulating GVHDR01CA173878 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI REDDY, PAVAN · 2013 to 2017
$1.6M
mTOR, Inflammation and Senescence of Hematopoietic Stem CellsR01AG036690 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZHENG, PAN · 2010 to 2014
$1.6M
Development of a Novel Strategy to Prevent Experimental GVHDR01CA143379 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI REDDY, PAVAN · 2010 to 2014
$739k
NCI NIH HHS CA-0173878NCI NIH HHS CA143379NCI NIH HHS R01 CA143379NCI NIH HHS R01 CA173878NCI NIH HHS R01 CA217156NHLBI NIH HHS HL-090775NHLBI NIH HHS R01 HL090775NIA NIH HHS R01 AG036690
6 · The paper itself

Abstract

Activation of sialic-acid-binding immunoglobulin-like lectin-G (Siglec-G) by noninfectious damage-associated molecular patterns controls innate immune responses. However, whether it also regulates T-cell-mediated adaptive immune responses is not known. Graft-versus-host reaction is a robust adaptive immune response caused by allogeneic hematopoietic cell transplantation that have been activated by antigen-presenting cells (APCs) in the context of damaged host tissues following allogeneic hematopoietic cell transplantation. The role of infectious and noninfectious pattern recognition receptor-mediated activation in the induction and aggravation of graft-versus-host disease (GVHD) is being increasingly appreciated. But the role of pathways that control innate immune responses to noninfectious stimuli in modulating GVHD has heretofore not been recognized. We report that Siglec-G expression on host APCs, specifically on hematopoietic cells, negatively regulates GVHD in multiple clinically relevant murine models. Mechanistic studies with various relevant Siglec-G and CD24 knockout mice and chimeric animals, along with rescue experiments with novel CD24 fusion protein demonstrate that enhancing the interaction between Siglec-G on host APCs with CD24 on donor T cells attenuates GVHD. Taken together, our data demonstrate that Siglec-G-CD24 axis, controls the severity of GVHD and suggest that enhancing this interaction may represent a novel strategy for mitigating GVHD.

Indexed as

AnimalsAntigen-Presenting CellsBone Marrow TransplantationCD24 AntigenDendritic CellsDisease Models, AnimalGene ExpressionGraft vs Host DiseaseInflammationLectinsMiceMice, KnockoutProtein BindingRadiationReceptors, Antigen, B-CellSeverity of Illness IndexCD24 AntigenLectinsReceptors, Antigen, B-CellSialic Acid Binding Immunoglobulin-like LectinsSiglecg protein, mouse

Identifiers

PMID24695850
PMCPMC4041170
OpenAlexW1967773389

What OpenQuestion holds

Textmetadata
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.