Evidence map›Paper›PMID 26063968›Full record

ArticleMediators of inflammation2015

Increased Migratory and Activation Cell Markers of Peripheral Blood Lymphocytes in an Experimental Model of Nephrotic Syndrome.

Wagner de Fátima Pereira, Gustavo Eustáquio Alvim Brito-Melo, Cláudia Martins Carneiro, Dirceu de Sousa Melo, Karine Beatriz Costa, Fábio Lourenço Tadeu Guimarães, Etel Rocha-Vieira, Érica Leandro Marciano Vieira, Ana Cristina Simões e Silva

Open access · goldAbstract read
In one paragraph

Article in Mediators of inflammation, 2015. 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
1.0field-weighted citation impact, top 25% 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, 9 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

9 authors at 3 institutions in 1 country.

Wagner de Fátima PereiraImmunology Laboratory, Integrated Health Research Center, Universidade Federal dos Vales do Jequitinhonha e Mucuri (UFVJM), 38610-000 Diamantina, MG, Brazil.
Gustavo Eustáquio Alvim Brito-MeloImmunology Laboratory, Integrated Health Research Center, Universidade Federal dos Vales do Jequitinhonha e Mucuri (UFVJM), 38610-000 Diamantina, MG, Brazil.
Cláudia Martins CarneiroImmunopathology Laboratory, Center for Research in Biological Sciences (LIMP/NUPEB), Universidade Federal de Ouro Preto (UFOP), 30140-081 Ouro Preto, MG, Brazil.
Dirceu de Sousa MeloImmunology Laboratory, Integrated Health Research Center, Universidade Federal dos Vales do Jequitinhonha e Mucuri (UFVJM), 38610-000 Diamantina, MG, Brazil.
Karine Beatriz CostaImmunology Laboratory, Integrated Health Research Center, Universidade Federal dos Vales do Jequitinhonha e Mucuri (UFVJM), 38610-000 Diamantina, MG, Brazil.
Fábio Lourenço Tadeu GuimarãesImmunology Laboratory, Integrated Health Research Center, Universidade Federal dos Vales do Jequitinhonha e Mucuri (UFVJM), 38610-000 Diamantina, MG, Brazil.
Etel Rocha-VieiraImmunology Laboratory, Integrated Health Research Center, Universidade Federal dos Vales do Jequitinhonha e Mucuri (UFVJM), 38610-000 Diamantina, MG, Brazil.
Érica Leandro Marciano VieiraInterdisciplinary Laboratory of Medical Investigation, Pediatric Nephrology Unit, Universidade Federal de Minas Gerais (UFMG), 30130-100 Belo Horizonte, MG, Brazil.
Ana Cristina Simões e SilvaInterdisciplinary Laboratory of Medical Investigation, Pediatric Nephrology Unit, Universidade Federal de Minas Gerais (UFMG), 30130-100 Belo Horizonte, MG, Brazil.
Universidade Federal dos Vales do Jequitinhonha e Mucuri · BRUniversidade Federal de Minas Gerais · BRUniversidade Federal de Ouro Preto · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study aimed to evaluate the expression of CD80 and CD18 in subpopulations of peripheral blood leukocytes and oxidative kidney damage in rats with nephrotic syndrome (NS) induced by doxorubicin (Dox) in comparison to control animals at different time points. Male adult Wistar rats were submitted to 24-hour urine and blood collection for biochemical and immunological analysis at 7, 14, 21, and 28 days after Dox injection. After euthanasia, the kidneys were removed for histological analysis and the evaluation of oxidative stress. The phenotypic characterization of leukocytes was performed using flow cytometry. Dox-injected animals exhibited increased CD18 expression in cytotoxic T lymphocytes, NK cells, and monocytes and high CD80 expression in monocytes. Kidney oxidative damage was positively correlated with CD80 expression in monocytes and serum levels of creatinine. These results suggest that phagocytic and cytotoxic cells are preferentially recruited to the tissue injury site, which may contribute to kidney dysfunction in this animal model of NS. The blockade of integrin and costimulatory molecules may provide new therapeutic opportunities for NS.

Indexed as

AnimalsB7-1 AntigenDoxorubicinFlow CytometryKidneyKiller Cells, NaturalLeukocytesMaleMonocytesNephrotic SyndromeOxidation-ReductionRatsRats, WistarT-Lymphocytes, CytotoxicB7-1 AntigenDoxorubicin

Identifiers

PMID26063968
PMCPMC4439504
OpenAlexW1577886803

What OpenQuestion holds

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LicenceCC BY
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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.