Evidence map›Paper›PMID 21051093›Full record

ArticleJournal of neuroimmunology2011

STAT6⁻/⁻ mice exhibit decreased cells with alternatively activated macrophage phenotypes and enhanced disease severity in murine neurocysticercosis.

Bibhuti B Mishra, Uma Mahesh Gundra, Judy M Teale

Open access · greenAbstract read
In one paragraph

Article in Journal of neuroimmunology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 41 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Bibhuti B MishraDepartment of Biology, South Texas Center for Emerging Infectious Diseases, University of Texas at San Antonio, One UTSA Circle, San Antonio, TX 78249-1644, United States.
Uma Mahesh Gundra
Judy M Teale
Texas Center for Infectious Disease · US

Funding

Tularemia: Pathogenesis and Host ResponseP01AI057986 · NIAID · UNIVERSITY OF TEXAS SAN ANTONIO · PI KLOSE, KARL E · 2005 to 2009
$6.1M
NEUROIMMUNOLOGY AND PATHOLOGY OF NEUROCYSTICERCOSISR01NS035974 · NINDS · UNIVERSITY OF TEXAS SAN ANTONIO · PI TEALE, JUDY M · 1997 to 2009
$2.7M
Effect of Aging on Immunity to TularemiaR01AI059703 · NIAID · UNIVERSITY OF TEXAS SAN ANTONIO · PI TEALE, JUDY M · 2004 to 2008
$1.7M
NIAID NIH HHS AI 59703NIAID NIH HHS P01 AI057986NIAID NIH HHS R01 AI059703NINDS NIH HHS NS 35974NINDS NIH HHS R01 NS035974
6 · The paper itself

Abstract

In this study, using a murine model for neurocysticercosis, macrophage phenotypes and their functions were examined. Mesocestoides corti infection in the central nervous system (CNS) induced expression of markers associated with alternatively activated macrophages (AAMs) and a scarcity of iNOS, a classically activated macrophage marker. The infection in STAT6(-/-) mice resulted in significantly reduced accumulation of AAMs as well as enhanced susceptibility to infection coinciding with increased parasite burden and greater neuropathology. These results demonstrate that macrophages in the helminth infected CNS are largely of AAM phenotypes, particularly as the infection progresses, and that STAT6 dependent responses, possibly involving AAMs, are essential for controlling neurocysticercosis.

Indexed as

AnimalsBrain DiseasesDisease Models, AnimalFemaleFluorescent Antibody TechniqueMacrophage ActivationMacrophagesMiceMice, Inbred C57BLMice, KnockoutNeurocysticercosisPhenotypeReverse Transcriptase Polymerase Chain ReactionSTAT6 Transcription FactorStat6 protein, mouseSTAT6 Transcription Factor

Identifiers

PMID21051093
PMCPMC3073530
OpenAlexW1980887274

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.