Evidence map›Paper›PMID 29201022›Full record

ArticleFrontiers in microbiology2017

Lays G S Bomfim, Lucas S Magalhães, Marcello A A Santos-Filho, Nalu T A Peres, Cristiane B Corrêa, Diego M Tanajura, Angela M Silva, Michael W Lipscomb, Valéria M Borges, Amélia R Jesus and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2017. 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
0.7field-weighted citation impact, top 32% 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, 18 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

12 authors at 3 institutions in 2 countries.

Lays G S BomfimLaboratório de Biologia Molecular-Hospital Universitário, Universidade Federal de Sergipe-Aracaju, Sergipe, Brazil.
Lucas S MagalhãesLaboratório de Biologia Molecular-Hospital Universitário, Universidade Federal de Sergipe-Aracaju, Sergipe, Brazil.
Marcello A A Santos-FilhoLaboratório de Biologia Molecular-Hospital Universitário, Universidade Federal de Sergipe-Aracaju, Sergipe, Brazil.
Nalu T A PeresLaboratório de Biologia Molecular-Hospital Universitário, Universidade Federal de Sergipe-Aracaju, Sergipe, Brazil.
Cristiane B CorrêaLaboratório de Biologia Molecular-Hospital Universitário, Universidade Federal de Sergipe-Aracaju, Sergipe, Brazil.
Diego M TanajuraLaboratório de Biologia Molecular-Hospital Universitário, Universidade Federal de Sergipe-Aracaju, Sergipe, Brazil.
Angela M SilvaLaboratório de Biologia Molecular-Hospital Universitário, Universidade Federal de Sergipe-Aracaju, Sergipe, Brazil.
Michael W LipscombDepartment of Biology, Howard University, Washington, DC, United States.
Valéria M BorgesInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Amélia R JesusLaboratório de Biologia Molecular-Hospital Universitário, Universidade Federal de Sergipe-Aracaju, Sergipe, Brazil.
Roque P AlmeidaLaboratório de Biologia Molecular-Hospital Universitário, Universidade Federal de Sergipe-Aracaju, Sergipe, Brazil.
Tatiana R de MouraLaboratório de Biologia Molecular-Hospital Universitário, Universidade Federal de Sergipe-Aracaju, Sergipe, Brazil.
Universidade Federal de Sergipe · BRFundação Oswaldo Cruz · BRHoward University · US

Funding

Crosstalk and the cytoskeleton in dendritic cell antigen presentationSC2GM103741 · NIGMS · HOWARD UNIVERSITY · PI LIPSCOMB, MICHAEL W · 2015 to 2017
$441k
NIGMS NIH HHS SC2 GM103741
6 · The paper itself

Abstract

Visceral leishmaniasis (VL) is a systemic transmissible disease that remains to be a major global health problem. The inflammatory response during VL is characterized by the release of several cytokines and other pro-inflammatory mediators. Triggering Receptor Expressed on Myeloid Cells (TREM) are a group of evolutionarily conserved membrane-bound surface receptors expressed on neutrophils and monocytes. Engagement of TREM-1 directs intracellular signaling events that drive cytokine production, degranulation, and phagocytosis. In certain inflammatory-associated diseases, TREM-1 can also be found as a soluble form (sTREM-1), which can negatively regulate TREM-1 receptor signaling. In these studies, we now find that high levels of circulating sTREM-1 correlate directly with VL disease severity. In particular, high levels of sTREM-1 were observed in non-survivor VL patients. Furthermore, these levels of sTREM-1 positively correlated with liver size and negatively correlated with leukocyte counts and hemoglobin concentration. Moreover, we found that neutrophils exposure

Indexed as

Leishmania infantumneutrophilssTREM-1TREM-1visceral leishmaniasis

Identifiers

PMID29201022
PMCPMC5696592
OpenAlexW2770834030

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.