Evidence map›Paper›PMID 31250049›Full record

ArticleImmunogenetics2019

The microstructure in the placenta is influenced by the functional diversity of HLA-G allelic variants.

F Stieglitz, A A Celik, C von Kaisenberg, M A Camps, R Blasczyk, Christina Bade-Döding

Open access · hybridAbstract read
In one paragraph

Article in Immunogenetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

8 citing papers in PubMed, 14 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

6 authors at 1 institution in 1 country.

F StieglitzHannover Medical School, Institute for Transfusion Medicine, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
A A CelikHannover Medical School, Institute for Transfusion Medicine, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
C von KaisenbergDepartment of Obstetrics and Gynecology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
M A CampsImusyn GmbH & Co. KG, Feodor-Lynen-Str. 5, 30625, Hannover, Germany.
R BlasczykHannover Medical School, Institute for Transfusion Medicine, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
Christina Bade-DödingHannover Medical School, Institute for Transfusion Medicine, Carl-Neuberg-Str. 1, 30625, Hannover, Germany. bade-doeding.christina@mh-hannover.de.
Medizinische Hochschule Hannover · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The main expression sites of HLA-G are human extravillous trophoblast cells. The interaction of HLA-G with uterine NK cells promotes their maturation and differentiation into decidual NK (dNK) cells. dNK cells secrete chemokines, cytokines, and proangiogenic factors in favor of a vascular remodeling and an immune suppressive microenvironment of the decidua. HLA-G is the most polymorphic member of the oligomorphic non-classical HLA molecule family; yet, the impact of polymorphic differences is not comprehensively understood. sHLA-G levels in embryo culture medium correlate with successful pregnancy; however, it remains questionable if HLA-G allelic diversity impacts on the outcome of dNK cell development. We utilized synthetic sHLA-G*01:01, 01:03, and 01:04 molecules and transduced K652/mHLA-G*01:01, 01:03, and 01:04 cells to study the biological interaction between HLA-G alleles and primary NK cells of human term placenta. Despite its low frequency, HLA-G*01:04 and not the most prevalent allele HLA-G*01:01 appear to be strong catalysts of dNK cell proliferation. Concluding, this study illustrates novel insights into the impact and binding efficiency of the three most common variants of HLA-G on primary placental NK cells.

Indexed as

CD56 AntigenCell ProliferationDeciduaFemaleHLA-G AntigensHumansK562 CellsKiller Cells, NaturalPlacentaPregnancyCD56 AntigenHLA-G AntigensNCAM1 protein, humanDeciduaDevelopmentdNK cellsHLA-GPlacentaPregnancy

Identifiers

PMID31250049
PMCPMC6647172
OpenAlexW2956122211

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.