Evidence map›Paper›PMID 31057553›Full record

ArticleFrontiers in immunology2019

The Checkpoint Regulator SLAMF3 Preferentially Prevents Expansion of Auto-Reactive B Cells Generated by Graft-vs.-Host Disease.

Ninghai Wang, Burcu Yigit, Cees E van der Poel, Marta Cuenca, Michael C Carroll, Roland W Herzog, Pablo Engel, Cox Terhorst

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. 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

8 authors at 4 institutions in 2 countries.

Ninghai WangDivision of Immunology, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA, United States.
Burcu YigitDivision of Immunology, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA, United States.
Cees E van der PoelProgram in Cellular and Molecular Medicine, Harvard Medical School, Boston Children's Hospital, Boston, MA, United States.
Marta CuencaHerman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, United States.
Michael C CarrollProgram in Cellular and Molecular Medicine, Harvard Medical School, Boston Children's Hospital, Boston, MA, United States.
Roland W HerzogHerman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, United States.
Pablo EngelImmunology Unit, Department of Cell Biology, Immunology and Neurosciences, Medical School, University of Barcelona, Barcelona, Spain.
Cox TerhorstDivision of Immunology, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA, United States.
Harvard University · USBoston Children's Hospital · USIndiana University – Purdue University Indianapolis · USUniversitat de Barcelona · ES

Funding

Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG · 1991 to 2026
$35.3M
The Slamf3, Slamf5, and Slamf6 receptor-induced pathways to murine lupusP01AI065687 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI SHARPE, ARLENE H. · 2006 to 2016
$14.7M
Enhancing immune regulation in gene therapy for hemophiliaR01HL131093 · NHLBI · UNIVERSITY OF FLORIDA · PI Ype Peter De Jong, Roland W. Herzog · 2016 to 2026
$7.2M
NHLBI NIH HHS R01 HL131093NIAID NIH HHS P01 AI065687NIDDK NIH HHS P30 DK043351
6 · The paper itself

Abstract

Absence of the mouse cell surface receptor SLAMF3 in SLAMF3-/- mice suggested that this receptor negatively regulates B cell homeostasis by modulating activation thresholds of B cell subsets. Here, we examine whether anti-SLAMF3 affects both B and T cell subsets during immune responses to haptenated ovalbumin [NP-OVA] and in the setting of chronic graft vs. host disease (cGVHD) induced by transferring B6.C-

Indexed as

Cell ProliferationAnimalsB-Lymphocyte SubsetsFemaleGerminal CenterGraft vs Host DiseaseMiceMice, KnockoutSignaling Lymphocytic Activation Molecule FamilySignal TransductionT-Lymphocytes, RegulatoryLy9 protein, mouseSignaling Lymphocytic Activation Molecule FamilyalloimmunityautoreactiveB cellscGVHDSLAMF3

Identifiers

PMID31057553
PMCPMC6482334
OpenAlexW2937211014

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.