Evidence map›Paper›PMID 30131391›Full record

ArticleDiabetes2018

Healthy Donor Polyclonal IgMs Diminish B-Lymphocyte Autoreactivity, Enhance Regulatory T-Cell Generation, and Reverse Type 1 Diabetes in NOD Mice.

Christopher S Wilson, Preeti Chhabra, Andrew F Marshall, Caleigh V Morr, Blair T Stocks, Emilee M Hoopes, Rachel H Bonami, Greg Poffenberger, Kenneth L Brayman, Daniel J Moore

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. NOD Mice Recapitulate the Cardiac Disturbances Observed in Type 1 Diabetes.Journal of cardiovascular translational research · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Christopher S WilsonDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN.
Preeti ChhabraDepartment of Surgery, University of Virginia, Charlottesville, VA.
Andrew F MarshallDepartment of Pediatrics, Ian Burr Division of Endocrinology and Diabetes, Vanderbilt University Medical Center, Nashville, TN.
Caleigh V MorrDepartment of Pediatrics, Ian Burr Division of Endocrinology and Diabetes, Vanderbilt University Medical Center, Nashville, TN.
Blair T StocksDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN.
Emilee M HoopesDepartment of Pediatrics, Ian Burr Division of Endocrinology and Diabetes, Vanderbilt University Medical Center, Nashville, TN.
Rachel H BonamiDepartment of Medicine, Division of Rheumatology and Immunology, Vanderbilt University Medical Center, Nashville, TN.
Greg PoffenbergerDepartment of Medicine, Division of Endocrinology, Vanderbilt University Medical Center, Nashville, TN.
Kenneth L BraymanDepartment of Surgery, University of Virginia, Charlottesville, VA.
Daniel J MooreDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN daniel.moore@vanderbilt.edu.ORCID 0000-0002-6889-9345
Vanderbilt University Medical Center · USUniversity of Virginia · US

Funding

Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DAVID H WASSERMAN · 2012 to 2026
$29.3M
Vanderbilt/Meharry Initiative for Minority Student DvptR25GM062459 · NIGMS · VANDERBILT UNIVERSITY · PI VELEZ EDWARDS, DIGNA R · 2002 to 2020
$10.4M
Building Interdisciplinary Research Careers in Women's HealthK12HD043483 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI HARTMANN, KATHERINE E, MAJOR, AMY S · 2002 to 2023
$10.3M
High Throughput Identification of Treg Activating MoleculesR21AI119224 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MOORE, DANIEL J. · 2015 to 2016
$427k
Targeting B lymphocyte Signaling to Reprogram Autoimmunity in Type 1 DiabetesF31DK107321 · NIDDK · VANDERBILT UNIVERSITY · PI WILSON, CHRISTOPHER S. · 2015 to 2017
$84k
NIAID NIH HHS R21 AI119224NICHD NIH HHS K12 HD043483NIDDK NIH HHS F31 DK107321NIDDK NIH HHS P30 DK020593NIGMS NIH HHS R25 GM062459
6 · The paper itself

Abstract

Autoimmune diseases such as type 1 diabetes (T1D) arise from unrestrained activation of effector lymphocytes that destroy target tissues. Many efforts have been made to eliminate these effector lymphocytes, but none has produced a long-term cure. An alternative to depletion therapy is to enhance endogenous immune regulation. Among these endogenous alternatives, naturally occurring Igs have been applied for inflammatory disorders but have lacked potency in antigen-specific autoimmunity. We hypothesized that naturally occurring polyclonal IgMs, which represent the majority of circulating, noninduced antibodies but are present only in low levels in therapeutic Ig preparations, possess the most potent capacity to restore immune homeostasis. Treatment of diabetes-prone NOD mice with purified IgM isolated from Swiss Webster (SW) mice (nIgM

Indexed as

AnimalsB-LymphocytesDiabetes Mellitus, Type 1Immunoglobulin MMiceMice, Inbred NODT-Lymphocytes, RegulatoryImmunoglobulin M

Identifiers

PMID30131391
PMCPMC6198348
OpenAlexW2888419086

What Socratic 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 Socratic graph.