Evidence map›Paper›PMID 21641401›Full record

ArticleThe American journal of pathology2011

Effect of macrophage migration inhibitory factor (MIF) in human placental explants infected with Toxoplasma gondii depends on gestational age.

Angelica de Oliveira Gomes, Deise Aparecida de Oliveira Silva, Neide Maria Silva, Bellisa de Freitas Barbosa, Priscila Silva Franco, Mariana Bodini Angeloni, Marise Lopes Fermino, Maria Cristina Roque-Barreira, Nicoletta Bechi, Luana Ricci Paulesu and 3 more

Abstract read
In one paragraph

Article in The American journal of pathology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

32 citing papers in PubMed, 79 citations in OpenAlex.

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  8. Galectin-3 plays a key role in controlling infection byFrontiers in cellular and infection microbiology · 2024
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  9. Modeling the human placental barrier to understandFrontiers in cellular and infection microbiology · 2023
    Review
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  13. Review
  14. Biogenic Silver Nanoparticles Can ControlFrontiers in microbiology · 2020
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  19. Cyclooxygenase (COX)-2 Inhibitors ReduceFrontiers in microbiology · 2019
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  20. IncreasedFrontiers in microbiology · 2019
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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

13 authors at 3 institutions in 2 countries.

Angelica de Oliveira GomesInstituto de Ciências Biomédicas, Universidade Federal de Uberlândia, Uberlândia, Minas Gerais, Brazil.
Deise Aparecida de Oliveira Silva
Neide Maria Silva
Bellisa de Freitas Barbosa
Priscila Silva Franco
Mariana Bodini Angeloni
Marise Lopes Fermino
Maria Cristina Roque-Barreira
Nicoletta Bechi
Luana Ricci Paulesu
Maria Célia Dos Santos
José Roberto Mineo
Eloisa Amália Vieira Ferro
Universidade Federal de Uberlândia · BRUniversidade de São Paulo · BRUniversity of Siena · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Because macrophage migration inhibitory factor (MIF) is a key cytokine in pregnancy and has a role in inflammatory response and pathogen defense, the objective of the present study was to investigate the effects of MIF in first- and third-trimester human placental explants infected with Toxoplasma gondii. Explants were treated with recombinant MIF, IL-12, interferon-γ, transforming growth factor-β1, or IL-10, followed by infection with T. gondii RH strain tachyzoites. Supernatants of cultured explants were assessed for MIF production. Explants were processed for morphologic analysis, immunohistochemistry, and real-time PCR analysis. Comparison of infected and stimulated explants versus noninfected control explants demonstrated a significant increase in MIF release in first-trimester but not third-trimester explants. Tissue parasitism was higher in third- than in first-trimester explants. Moreover, T. gondii DNA content was lower in first-trimester explants treated with MIF compared with untreated explants. However, in third-trimester explants, MIF stimulus decreased T. gondii DNA content only at the highest concentration of the cytokine. In addition, high expression of MIF receptor was observed in first-trimester placental explants, whereas MIF receptor expression was low in third-trimester explants. In conclusion, MIF was up-regulated and demonstrated to be important for control of T. gondii infection in first-trimester explants, whereas lack of MIF up-regulation in third-trimester placentas may be involved in higher susceptibility to infection at this gestational age.

Indexed as

Gestational AgeAntigens, Differentiation, B-LymphocyteFemaleGene Expression RegulationHistocompatibility Antigens Class IIHumansIntramolecular OxidoreductasesMacrophage Migration-Inhibitory FactorsModels, BiologicalNitritesPlacentaPregnancyPregnancy Trimester, FirstPregnancy Trimester, ThirdToxoplasmaToxoplasmosisAntigens, Differentiation, B-LymphocyteHistocompatibility Antigens Class IIIntramolecular Oxidoreductasesinvariant chainMacrophage Migration-Inhibitory FactorsMIF protein, humanNitrites

Identifiers

PMID21641401
PMCPMC3124335
OpenAlexW2019463902

What OpenQuestion 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 OpenQuestion graph.