Evidence map›Paper›PMID 26733206›Full record

ArticleScientific reports2016

VIP treatment prevents embryo resorption by modulating efferocytosis and activation profile of maternal macrophages in the CBAxDBA resorption prone model.

Lucila Gallino, Guillermina Calo, Vanesa Hauk, Laura Fraccaroli, Esteban Grasso, Mónica Vermeulen, Claudia Pérez Leirós, Rosanna Ramhorst

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
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

8 authors at 4 institutions in 2 countries.

Lucila GallinoImmunopharmacology Laboratory, School of Sciences, University of Buenos Aires. IQUIBICEN-CONICET.
Guillermina CaloImmunopharmacology Laboratory, School of Sciences, University of Buenos Aires. IQUIBICEN-CONICET.
Vanesa HaukImmunopharmacology Laboratory, School of Sciences, University of Buenos Aires. IQUIBICEN-CONICET.
Laura FraccaroliImmunopharmacology Laboratory, School of Sciences, University of Buenos Aires. IQUIBICEN-CONICET.
Esteban GrassoImmunopharmacology Laboratory, School of Sciences, University of Buenos Aires. IQUIBICEN-CONICET.
Mónica VermeulenInstitute of Experimental Medicine IMEX-CONICET, National Academy of Sciences, Buenos Aires.
Claudia Pérez LeirósImmunopharmacology Laboratory, School of Sciences, University of Buenos Aires. IQUIBICEN-CONICET.
Rosanna RamhorstImmunopharmacology Laboratory, School of Sciences, University of Buenos Aires. IQUIBICEN-CONICET.
Instituto de Química y Fisicoquímica Biológicas · ARConsejo Nacional de Investigaciones Científicas y Técnicas · ARCzech Academy of Sciences, Institute of Experimental Medicine · CZUniversity of Buenos Aires · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Successful embryo implantation occurs followed by a local pro-inflammatory response subsequently shifted toward a tolerogenic one. VIP (vasoactive intestinal peptide) has embryotrofic, anti-inflammatory and tolerogenic effects. In this sense, we investigated whether the in vivo treatment with VIP contributes to an immunosuppressant local microenvironment associated with an improved pregnancy outcome in the CBA/J × DBA/2 resorption prone model. Pregnancy induced the expression of VIP, VPAC1 and VPAC2 in the uterus from CBA/J × DBA/2 mating females on day 8.5 of gestation compared with non-pregnant mice. VIP treatment (2 nmol/mouse i.p.) on day 6.5 significantly increased the number of viable implantation sites and improved the asymmetric distribution of implanted embryos. This effect was accompanied by a decrease in RORγt and an increase in TGF-β and PPARγ expression at the implantation sites. Moreover, VIP modulated the maternal peritoneal macrophages efferocytosis ability, tested using latex beads-FITC or apoptotic thymocytes, displaying an increased frequency of IL-10-producer F4/80 cells while did not modulate TNF-α and IL-12 secretion. The present data suggest that VIP treatment increases the number of viable embryos associated with an increase in the efferocytic ability of maternal macrophages which is related to an immunosuppressant microenvironment.

Indexed as

AnimalsCellular MicroenvironmentCytokinesEmbryo ImplantationFemaleMacrophagesMaleMiceMice, Inbred CBAMice, Inbred DBANuclear Receptor Subfamily 1, Group F, Member 3PhagocytosisReceptors, Vasoactive Intestinal PeptideVasoactive Intestinal PeptideCytokinesNuclear Receptor Subfamily 1, Group F, Member 3Receptors, Vasoactive Intestinal PeptideVasoactive Intestinal Peptide

Identifiers

PMID26733206
PMCPMC4702085
OpenAlexW2229443118

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.