Evidence map›Paper›PMID 33013937›Full record

ArticleFrontiers in immunology2020

NK and T Cell Differentiation at the Maternal-Fetal Interface in Sows During Late Gestation.

Melissa R Stas, Michaela Koch, Maria Stadler, Spencer Sawyer, Elena L Sassu, Kerstin H Mair, Armin Saalmüller, Wilhelm Gerner, Andrea Ladinig

Abstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Immunological uterine response to pig embryos before and during implantation.Reproduction in domestic animals = Zuchthygiene · 2022
    Review
  8. Review
  9. Review
  10. Article
  11. 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

9 authors.

Melissa R StasUniversity Clinic for Swine, Department for Farm Animals and Veterinary Public Health, University of Veterinary Medicine Vienna, Vienna, Austria.
Michaela KochUniversity Clinic for Swine, Department for Farm Animals and Veterinary Public Health, University of Veterinary Medicine Vienna, Vienna, Austria.
Maria StadlerInstitute of Immunology, Department of Pathobiology, University of Veterinary Medicine Vienna, Vienna, Austria.
Spencer SawyerUniversity Clinic for Swine, Department for Farm Animals and Veterinary Public Health, University of Veterinary Medicine Vienna, Vienna, Austria.
Elena L SassuUniversity Clinic for Swine, Department for Farm Animals and Veterinary Public Health, University of Veterinary Medicine Vienna, Vienna, Austria.
Kerstin H MairInstitute of Immunology, Department of Pathobiology, University of Veterinary Medicine Vienna, Vienna, Austria.
Armin SaalmüllerInstitute of Immunology, Department of Pathobiology, University of Veterinary Medicine Vienna, Vienna, Austria.
Wilhelm GernerInstitute of Immunology, Department of Pathobiology, University of Veterinary Medicine Vienna, Vienna, Austria.
Andrea LadinigUniversity Clinic for Swine, Department for Farm Animals and Veterinary Public Health, University of Veterinary Medicine Vienna, Vienna, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The phenotype and function of immune cells that reside at the maternal-fetal interface in humans and mice have been, and still are, extensively studied with the aim to fully comprehend the complex immunology of pregnancy. In pigs, information regarding immune cell phenotypes is limited and mainly focused on early gestation whereas late gestation has not yet been investigated. We designed a unique methodology tailored to the porcine epitheliochorial placenta, which allowed us to address immune phenotypes separately in the maternal endometrium (ME) and fetal placenta (FP) by flow cytometry. In-depth phenotyping of NK cells, non-conventional and conventional T cells within maternal blood (mBld), ME, FP, and fetal spleen (fSpln) revealed major differences between these anatomic sites. In both maternal compartments, all NK cells were perforin

Indexed as

AnimalsCell DifferentiationCells, CulturedFemaleImmunologic MemoryKiller Cells, NaturalLeukocytes, MononuclearLymphocyte ActivationMaternal-Fetal RelationsPerforinPlacentaPregnancyReceptors, Antigen, T-Cell, gamma-deltaSwineT-LymphocytesPerforinReceptors, Antigen, T-Cell, gamma-deltaCD4 T cellsCD8 T cellsflow cytometrylate gestationnatural killer cellsporcine placenta

Identifiers

PMID33013937
PMCPMC7516083

What OpenQuestion holds

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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.