Differential circulating CD8+ memory T-cell activation profiles in nulliparous and multiparous women undergoing induction of labor

Abstract Multiparous women typically give birth faster than nulliparous women, but the exact mechanisms underlying this differential speed remain unclear. As multiparous women have elevated inflammatory mediators in gestational tissues and circulation compared to nulliparous women, immunological memory acquired from prior childbirth may contribute to these differences. We conducted a prospective longitudinal study involving 34 nulliparous and 30 multiparous women undergoing induction of labor (IOL). Maternal peripheral blood samples were collected at three time points: before IOL, during the latent phase, and during the active phase of labor. Circulating CD8⁺ memory T-cell subsets—including central memory (T CM ), stem cell memory (T SCM ), effector memory (T EM ), terminally differentiated effector memory (T EMRA ), and CXCR5⁺ memory T-cells (T CXCR5⁺ )—as well as their activated populations (indicated by CD69⁺ expression), were analyzed using multicolor flow cytometry. Comparisons between parity groups and across sampling time points were analyzed using linear mixed-effects models. Longitudinal analysis showed that multiparous women exhibited elevated percentages of activated TEM cells and activated TEM cells after IOL, which were higher than those observed in nulliparous women, whereas nulliparous women showed reduced total TCM percentages after IOL ( P < 0.05). These findings suggest parity-associated differences in circulating CD8⁺ memory T-cell activation profiles during IOL.

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Publication Details

Journal
Scientific Reports
Published
2026-08-25
DOI
https://doi.org/10.1038/s41598-026-67715-3
Primary Topic
Reproductive System and Pregnancy
Type
article
Field-Weighted Citation Impact
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article

Differential circulating CD8+ memory T-cell activation profiles in nulliparous and multiparous women undergoing induction of labor

Xiaoyi Bai, Tak Yeung Leung, Chi Chiu Wang, Wenjing Ding et al.
Scientific Reports
Reproductive System and Pregnancy
article

Differential circulating CD8+ memory T-cell activation profiles in nulliparous and multiparous women undergoing induction of labor

Xiaoyi Bai, Tak Yeung Leung, Chi Chiu Wang, Wenjing Ding, Olena Getsko, Tao Zhang, Yue Wang
article en

Abstract

Abstract Multiparous women typically give birth faster than nulliparous women, but the exact mechanisms underlying this differential speed remain unclear. As multiparous women have elevated inflammatory mediators in gestational tissues and circulation compared to nulliparous women, immunological memory acquired from prior childbirth may contribute to these differences. We conducted a prospective longitudinal study involving 34 nulliparous and 30 multiparous women undergoing induction of labor (IOL). Maternal peripheral blood samples were collected at three time points: before IOL, during the latent phase, and during the active phase of labor. Circulating CD8⁺ memory T-cell subsets—including central memory (T CM ), stem cell memory (T SCM ), effector memory (T EM ), terminally differentiated effector memory (T EMRA ), and CXCR5⁺ memory T-cells (T CXCR5⁺ )—as well as their activated populations (indicated by CD69⁺ expression), were analyzed using multicolor flow cytometry. Comparisons between parity groups and across sampling time points were analyzed using linear mixed-effects models. Longitudinal analysis showed that multiparous women exhibited elevated percentages of activated TEM cells and activated TEM cells after IOL, which were higher than those observed in nulliparous women, whereas nulliparous women showed reduced total TCM percentages after IOL ( P < 0.05). These findings suggest parity-associated differences in circulating CD8⁺ memory T-cell activation profiles during IOL.

Scientific Reports
Uppsala University (SE), Odessa National Medical University (UA), Chinese University of Hong Kong (HK)
Research Grants Council, University Grants Committee
Gender equality
Openalex Percentile: Top 16%
Reproductive System and Pregnancy
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