Evidence map›Paper›PMID 42893527›Full record

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

BeWo-Derived Extracellular Vesicles Downregulate IL-6Rα Expression via miRNAs on CD4+ T Lymphocytes.

Gábor Seregélyes, Bence Nagy, Árpád Ferenc Kovács, Nóra Fekete, Edit I Buzás, Éva Pállinger

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. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Gábor SeregélyesInstitute of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.ORCID https://orcid.org/0009-0007-6558-638X
Bence NagyInstitute of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.
Árpád Ferenc KovácsHeart and Vascular Center, Semmelweis University, Budapest, Hungary.ORCID https://orcid.org/0000-0002-7742-160X
Nóra FeketeInstitute of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.ORCID https://orcid.org/0000-0001-9721-765X
Edit I BuzásInstitute of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.ORCID https://orcid.org/0000-0002-3744-206X
Éva PállingerInstitute of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.ORCID https://orcid.org/0000-0002-5789-0951

Funding

STIA_2024 19279/PMKP/2025
6 · The paper itself

Abstract

problemA balanced Th1/Th2/Th17/Treg status is necessary for a successful pregnancy. T cell polarization depends on the local cytokine environment and the responsiveness of T lymphocytes to cytokines. Trophoblast-derived extracellular vesicles (EVs) influence the function of maternal T lymphocytes, contributing to their polarization into the Treg phenotype. We examined whether BeWo-derived EVs affect T cell IL-6 responsiveness using the BeWo cell line as an experimental model and characterized the molecular cargo of BeWo -EVs that may contribute to this process.

methodsCirculating lymphocytes from non-pregnant women were treated with BeWo-EVs or co-cultured with BeWo cells. We detected IL-6Rα expression by flow cytometry and IL6R signaling pathways by RT-PCR. The microRNA (miRNA) content of BeWo EVs was identified by sequencing. Finally, we compared IL-6Rα expression levels in circulating T lymphocytes from healthy pregnant and non-pregnant women.

resultsBeWo-EVs reduced IL-6Rα expression on CD4+ T cells. This modifies the IL-6 pathway by downregulating the transcription factors STAT3, NFKB1, and PIAS3 while upregulating STAT1. This may be due to the presence of specific microRNAs (miRNAs), such as hsa-mir-92a-3p, hsa-mir-520f-3p, and hsa-mir-25-3p, in BeWo-EVs that target the IL-6 pathway. Treatment with BeWo-EVs also induced phenotypic and functional changes in T cells and enhanced the ratio of CD4+/CD25+ T cells that produce IL-10. Pregnancy-associated IL-6Rα downregulation has been demonstrated in clinical samples. Significantly lower levels of IL-6Rα were detected on circulating CD4+CD25+ T cells in healthy pregnant women compared to healthy non-pregnant individuals.

conclusionsOur studies suggest that the microRNA content of trophoblast-derived EVs significantly influences the local polarization of maternal T lymphocytes by modifying the IL-6Rα signaling pathway.

Indexed as

CD4-Positive T-LymphocytesExtracellular VesiclesMicroRNAsReceptors, Interleukin-6TrophoblastsAdultCell Line, TumorDown-RegulationFemaleHumansInterleukin-6PregnancySignal TransductionSTAT3 Transcription FactorIL6R protein, humanInterleukin-6MicroRNAsReceptors, Interleukin-6STAT3 protein, humanSTAT3 Transcription FactorCD4+ T cellsextracellular vesicleshuman pregnancyIL‐6 pathwayIL‐6Rαimmune toleranceinterleukin‐6miRNAregulatory T cells

Identifiers

PMID42893527
PMCPMC13677083

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