Evidence map›Paper›PMID 29330323›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2018

IL-10 Deficiency Reveals a Role for TLR2-Dependent Bystander Activation of T Cells in Lyme Arthritis.

Sarah K Whiteside, Jeremy P Snook, Ying Ma, F Lynn Sonderegger, Colleen Fisher, Charisse Petersen, James F Zachary, June L Round, Matthew A Williams, Janis J Weis

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

33 citing papers in PubMed, 40 citations in OpenAlex.

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  20. Immune Response toCurrent issues in molecular biology · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Sarah K WhitesideDepartment of Pathology, University of Utah, Salt Lake City, UT 84112; and.ORCID 0000-0003-4354-4713
Jeremy P SnookDepartment of Pathology, University of Utah, Salt Lake City, UT 84112; and.ORCID 0000-0002-1396-9254
Ying MaDepartment of Pathology, University of Utah, Salt Lake City, UT 84112; and.
F Lynn SondereggerDepartment of Pathology, University of Utah, Salt Lake City, UT 84112; and.
Colleen FisherDepartment of Pathology, University of Utah, Salt Lake City, UT 84112; and.ORCID 0000-0002-3688-6283
Charisse PetersenDepartment of Pathology, University of Utah, Salt Lake City, UT 84112; and.ORCID 0000-0003-4045-2610
James F ZacharyDepartment of Pathobiology, University of Illinois at Urbana-Champaign, Urbana, IL 61802.
June L RoundDepartment of Pathology, University of Utah, Salt Lake City, UT 84112; and.
Matthew A WilliamsDepartment of Pathology, University of Utah, Salt Lake City, UT 84112; and.
Janis J WeisDepartment of Pathology, University of Utah, Salt Lake City, UT 84112; and Janis.weis@path.utah.edu.ORCID 0000-0001-7214-5987
University of Utah · USUniversity of Illinois Urbana-Champaign · US

Funding

MOLECULAR GENETICS OF LYME ARTHRITIS SUSCEPTIBILITYR01AR043521 · NIAMS · UNIVERSITY OF UTAH · PI WEIS, JANIS J. · 1994 to 2024
$9.4M
BORRELIA BURGDORFERI MITOGEN IN DEVELOPMENT OF ARTHRITISR01AI032223 · NIAID · UNIVERSITY OF UTAH · PI WEIS, JANIS J. · 1993 to 2023
$7.8M
Training Program in Microbial PathogenesisT32AI055434 · NIAID · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI MULVEY, MATTHEW A, PLANELLES, VICENTE · 2004 to 2025
$6.0M
Developing therapies to target the microbiotaDP2AT008746 · NCCIH · UNIVERSITY OF UTAH · PI ROUND, JUNE LOUISE · 2014 to 2014
$2.2M
Univ of Utah Cell Sorter for Flow Cytometry CoreS10RR026802 · NCRR · UNIVERSITY OF UTAH · PI GREEN, WAYNE FRANCIS · 2010 to 2010
$500k
Exploring the function of a novel, microbiota-regulated gene in T cellsR21AI109122 · NIAID · UNIVERSITY OF UTAH · PI ROUND, JUNE LOUISE · 2014 to 2015
$410k
Role of Zfp318 in the functional development of B cellsR21AI114462 · NIAID · UNIVERSITY OF UTAH · PI WEIS, JANIS J. · 2015 to 2016
$410k
The role of T cell intrinsic TLR signaling on host-commensal interactionsR56AI107090 · NIAID · UNIVERSITY OF UTAH · PI ROUND, JUNE LOUISE · 2013 to 2013
$350k
Exploring the mechanisms of T cell intrinsic TLR2 signaling on Treg functionK22AI095375 · NIAID · UNIVERSITY OF UTAH · PI ROUND, JUNE LOUISE · 2012 to 2013
$270k
HIV VACCINE PRODUCTIONN01AI095375 · NIAID · SRI INTERNATIONAL · PI KUNG, ADA P · 1999 to 2000
$61k
NCCIH NIH HHS DP2 AT008746NCRR NIH HHS S10 RR026802NIAID NIH HHS K22 AI095375NIAID NIH HHS N01 AI095375NIAID NIH HHS R01 AI032223NIAID NIH HHS R21 AI109122NIAID NIH HHS R21 AI114462NIAID NIH HHS R56 AI107090NIAID NIH HHS T32 AI055434NIAMS NIH HHS R01 AR043521
6 · The paper itself

Abstract

T cells predominate the immune responses in the synovial fluid of patients with persistent Lyme arthritis; however, their role in Lyme disease remains poorly defined. Using a murine model of persistent Lyme arthritis, we observed that bystander activation of CD4

Indexed as

AnimalsFemaleInterleukin-10Lyme DiseaseLymphocyte ActivationMaleMiceMice, Inbred C57BLMice, TransgenicT-LymphocytesToll-Like Receptor 2IL10 protein, mouseInterleukin-10Tlr2 protein, mouseToll-Like Receptor 2

Identifiers

PMID29330323
PMCPMC5809275
OpenAlexW2783615160

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.