Evidence map›Paper›PMID 34738274›Full record

ArticleAmerican journal of reproductive immunology (New York, N.Y. : 1989)2022

Uncomplicated oocyte donation pregnancies display an elevated CD163-positive type 2 macrophage load in the decidua, which is associated with fetal-maternal HLA mismatches.

Xuezi Tian, Kaveri T S Aiyer, Johanna M Kapsenberg, Dave L Roelen, Marie-Louise van der Hoorn, Michael Eikmans

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in American journal of reproductive immunology (New York, N.Y. : 1989), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07263490 (PRIOR Study), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 45% 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.

NCT07263490 recruitingnot on this mapstarted 2024, after this paper: background citation

PRIOR Study (Pre-eclampsia Risk In Oocyte Recipients) - Investigating Matching, Biomarkers and Outcomes.

TypeobservationalSponsorCopenhagen University Hospital, HvidovreRan2024 to 2028Enrolled462ConditionsPre-eclampsia, Oocyte Donation, Pre-Eclampsia, Complicating Pregnancy
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 9 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.

Xuezi TianDepartment of Obstetrics and Gynecology, Leiden University Medical Center, Leiden, Netherlands.ORCID 0000-0003-4620-5338
Kaveri T S AiyerDepartment of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Johanna M KapsenbergDepartment of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Dave L RoelenDepartment of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Marie-Louise van der HoornDepartment of Obstetrics and Gynecology, Leiden University Medical Center, Leiden, Netherlands.
Michael EikmansDepartment of Immunology, 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

problemThe embryo of an oocyte donation (OD) pregnancy is completely allogeneic to the mother, which may challenge the maternal immune system to tolerize the fetus. Decidual macrophages are essential in maintaining a healthy pregnancy, and type 2 macrophages may exhibit immune suppressive activity. We hypothesized that the composition of decidual macrophages is different between uncomplicated OD pregnancies and non-OD in vitro fertilization (IVF) pregnancies, and is related to fetal-maternal incompatibility. METHOD OF STUDY: Women with uncomplicated pregnancy were enrolled: 25 singleton OD pregnancies and 17 non-OD IVF pregnancies. The extent of immunohistochemical staining of CD14 (pan-macrophage marker) and CD163 (type 2 macrophage marker) in both decidua basalis and parietalis was quantitated by digital image analysis. Maternal and fetal DNA was typed for human leukocyte antigen (HLA)-A, -B, C, -DRB1, and -DQB1, and fetal-maternal HLA mismatches were calculated.

resultsOD pregnancies showed a higher percentage of CD163+ staining (P = .040) and higher CD163/CD14 ratio (P = .032) in the parietalis than non-OD IVF. The OD group was separated into a semi-allogeneic group (≤5 fetal maternal HLA mismatches) and a fully allogeneic group (> 5 mismatches). The HLA-fully-allogeneic OD group, but not the HLA-semi-allogeneic OD group, showed significantly elevated CD163/CD14 ratio in the parietalis compared with the non-OD IVF group (P < .05).

conclusionsUncomplicated OD pregnancies display a higher CD163-positive cell fraction in the total decidual macrophage population compared to autologous pregnancies, which may suggest that a local type 2 macrophage-related mechanism is needed to compensate for the higher fetal-maternal HLA mismatch load.

Indexed as

Oocyte DonationAdultAntigens, CDAntigens, Differentiation, MyelomonocyticCD163 AntigenDeciduaFemaleHumansImmune ToleranceMacrophagesPregnancyReceptors, Cell SurfaceAntigens, CDAntigens, Differentiation, MyelomonocyticCD163 AntigenReceptors, Cell SurfacedeciduaHLA antigensmacrophagesoocyte donationpregnancy

Identifiers

PMID34738274
PMCPMC9286476
OpenAlexW3208678243

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Registered trials

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