Evidence map›Paper›PMID 34054856›Full record

ArticleFrontiers in immunology2021

Maternal-Fetal HLA Compatibility in Uncomplicated and Preeclamptic Naturally Conceived Pregnancies.

Liseanne J van 't Hof, Naomi Schotvanger, Geert W Haasnoot, Carin van der Keur, Dave L Roelen, Lisa E E L O Lashley, Frans H J Claas, Michael Eikmans, Marie-Louise P van der Hoorn

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Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

13 citing papers in PubMed, 15 citations in OpenAlex.

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  11. Single cell RNA sequencing research in maternal fetal interface.Frontiers in cell and developmental biology · 2022
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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 1 institution in 1 country.

Liseanne J van 't HofDepartment of Obstetrics and Gynaecology, Leiden University Medical Center, Leiden, Netherlands.
Naomi SchotvangerDepartment of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Geert W HaasnootDepartment of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Carin van der KeurDepartment of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Dave L RoelenDepartment of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Lisa E E L O LashleyDepartment of Obstetrics and Gynaecology, Leiden University Medical Center, Leiden, Netherlands.
Frans H J ClaasDepartment of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Michael EikmansDepartment of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Marie-Louise P van der HoornDepartment of Obstetrics and Gynaecology, Leiden University Medical Center, Leiden, Netherlands.
Leiden University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: In pregnancy, the mother and fetus differ in HLA antigens, and yet the maternal immune system generally tolerates the fetus. KIR receptors expressed by maternal uterine NK cells at the maternal-fetal interface directly interact with HLA-C on extravillous trophoblast cells for optimal placental development. In this study, we aimed to determine whether there is a preferential selection for HLA compatibility and specific KIR/HLA-C combinations in uncomplicated and preeclamptic naturally conceived pregnancies compared to what would be expected by chance. Methods: Genotyping for maternal and fetal HLA-A, -B, -C, -DR, and -DQ, and maternal KIR was performed for 451 uncomplicated pregnancies and 77 pregnancies complicated with preeclampsia. The number of HLA antigen (mis)matches between mother and fetus was calculated and compared to expected values obtained by randomization of the HLA haplotype, inherited from the father, over the existing maternal haplotype of the fetuses. A similar methodology was executed for analysis of the KIR/HLA-C data (n=309). Results: In uncomplicated pregnancies, the degree of maternal-fetal HLA matching was not different than expected-by-chance values. In preeclamptic pregnancies, the degree of maternal-fetal HLA matching was different in observed compared to expected-by-chance values (p=0.012). More specifically, the degree of maternal-fetal matching of HLA-C was higher in the actual preeclamptic pregnancies than was expected-by-chance (p=0.007). Preeclamptic pregnancies showed an overall tendency towards higher maternal-fetal HLA compatibility, for total HLA matches (p=0.021), HLA class I (p=0.038) and HLA-C (p=0.025) compared to uncomplicated pregnancies. Conclusion: The data suggest that there is no preferential selection of maternal-fetal HLA compatibility in uncomplicated pregnancies. In contrast, increased total HLA, HLA class I and, especially, HLA-C compatibility is associated with preeclampsia, suggestive for a role of HLA mismatches in immune regulation leading to uncomplicated pregnancy.

Indexed as

AdultFemaleHistocompatibility, Maternal-FetalHLA AntigensHumansImmune PrivilegePre-EclampsiaPregnancyReceptors, KIRHLA AntigensReceptors, KIRHLA compatibilityhuman leukocyte antigenkiller-cell Immunoglobin-like receptorpreeclampsiapregnancyreproductive immunology

Identifiers

PMID34054856
PMCPMC8155594
OpenAlexW3160460446

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Registered trials

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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.