Evidence map›Paper›PMID 41782473›Full record

ArticleAmerican journal of reproductive immunology (New York, N.Y. : 1989)2026

T-bet Fate Mapping Reveals Gestational Stage-Specific Transcriptional Adaptation of Decidual NK Cells.

Mona A Mohamed, Yan Li, Andrea K Wegrzynowicz, Payton N Lindner, Jessica Vazquez, Gladys E Lopez, Aleksandar K Stanic

Abstract read
In one paragraph

Article in American journal of reproductive immunology (New York, N.Y. : 1989), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

7 authors.

Mona A MohamedDivision of Reproductive Sciences, Department of Obstetrics and Gynecology, University of Wisconsin-Madison, Madison, Wisconsin, USA.ORCID 0009-0006-4014-887X
Yan LiDivision of Reproductive Sciences, Department of Obstetrics and Gynecology, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Andrea K WegrzynowiczDivision of Reproductive Sciences, Department of Obstetrics and Gynecology, University of Wisconsin-Madison, Madison, Wisconsin, USA.ORCID 0000-0002-1493-4563
Payton N LindnerDivision of Reproductive Sciences, Department of Obstetrics and Gynecology, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Jessica VazquezDivision of Reproductive Sciences, Department of Obstetrics and Gynecology, University of Wisconsin-Madison, Madison, Wisconsin, USA.ORCID 0000-0002-8052-3850
Gladys E LopezDivision of Reproductive Sciences, Department of Obstetrics and Gynecology, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Aleksandar K StanicDivision of Reproductive Sciences, Department of Obstetrics and Gynecology, University of Wisconsin-Madison, Madison, Wisconsin, USA.ORCID 0000-0003-1946-6436

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Justine Yang Bruce · 1985 to 2026
$142.6M
Integrated Program in Endocrinology Translational Postdoctoral Training ProgramT32HD101384 · NICHD · UNIVERSITY OF WISCONSIN-MADISON · PI IAN M. BIRD, Jon E Levine · 2021 to 2026
$2.0M
Sterile Inflammation at the Maternal-Fetal Interface and Fetal Immune Programming in a Non-Human Primate ModelK01AI182448 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI Jessica Vazquez · 2024 to 2026
$658k
Gestationally driven trafficking of decidual lymphocytes assessed by serial intravascular stainingR21AI175753 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI STANIC-KOSTIC, ALEKSANDAR · 2023 to 2024
$428k
Burroughs Welcome Fund 1019835March of Dimes Basil O'Connor Scholar Award 5-FY18-541NIAID NIH HHS K01 AI182448NIAID NIH HHS R21AI175753NICHD NIH HHS L70 HD119811NICHD NIH HHS T32 HD101384NIH HHS 1S100OD018202-01NIH HHS 1S10RR025483-01NIH HHS K12HD000849-28NIH HHS P30 CA014520NIH HHS T32HD101384
6 · The paper itself

Abstract

problemNatural killer (NK) cells are critical regulators of immune balance at the maternal-fetal interface. T-bet (Tbx21) is a key transcription factor shaping NK cell effector functions, yet its role in decidual NK (dNK) cell adaptation across gestation remains unclear. METHOD OF STUDY: We used a T-bet fate-mapping mouse model (Rosa26

resultsWe found that NK cells with a history of T-bet expression (RFP+) progressively downregulate T-bet in a tissue and gestation-specific manner, particularly within decidual and placental compartments. Despite this loss, RFP+ cells retained core NK cell markers and altered their lineage identity towards ILC2 or ILC3 fate. Bulk transcriptomic analysis revealed that T-bet downregulation is associated with dampened IFN-γ, and cytotoxic pathways and increased expression of tissue-residency associated transcriptional regulators. Single-cell RNAseq revealed a gestational transition in dNK subset composition, with a decline in cytotoxic tissue-resident NK cells and expansion of regulatory and conventional NK subsets by late gestation.

conclusionsThese findings identify a novel transcriptional program that shapes NK cell plasticity in response to T-bet downregulation across gestation. Rather than undergoing lineage diversion, dNK cells adapt to the decidual environment via transcriptional compensation and subset redistribution during pregnancy. This work sheds light on the temporal coordination of innate immune function relevant to pregnancy success.

Indexed as

DeciduaKiller Cells, NaturalT-Box Domain ProteinsAnimalsCell LineageFemaleMicePlacentaPregnancyT-bet Transcription FactorTranscription, GeneticT-bet Transcription FactorT-Box Domain ProteinsdNKfate mappingpregnancyT‐bet

Identifiers

PMID41782473
PMCPMC12961421

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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.