# Revealing the immune landscape of menstrual blood: unlocking insights into activation, exhaustion, and mitochondrial mass for reproductive health

**Authors:** Oliver Richards, Megan Cotterell, Catherine A Thornton, April Rees

PMC · DOI: 10.1093/immhor/vlag013 · 2026-03-25

## TL;DR

This study uses menstrual blood to explore immune cell profiles and metabolism in reproductive health, revealing distinct immune patterns in conditions like endometriosis and PCOS.

## Contribution

The study introduces a high-dimensional flow cytometry method to analyze immune cell activation, exhaustion, and mitochondrial mass in menstrual blood.

## Key findings

- Menstrual blood has a unique immune profile with tissue-resident cells and distinct mitochondrial mass compared to peripheral blood.
- Endometriosis and PCOS show disease-specific immune trends, though not always statistically significant due to small sample size.
- Menstrual blood is proposed as a non-invasive sample for studying immune-related reproductive disorders and discovering biomarkers.

## Abstract

Reproductive disorders such as endometriosis and polycystic ovary syndrome (PCOS) are increasingly recognized as immune-mediated conditions, yet their immunopathology remains poorly understood. Menstrual blood, a noninvasive and biologically relevant sample, offers a unique window into reproductive tract immunity but has been underutilized in this context. We optimized Cytek’s® 25-color high-dimensional flow cytometry panel by incorporating a mitochondrial dye to investigate immune cell profiles in menstrual mononuclear cells (MMCs) from healthy individuals, and those with endometriosis or PCOS, in comparison with matched peripheral blood mononuclear cells (PBMCs). This enabled detailed assessment of 40 immune cell subsets and 546 immunological parameters, including markers of activation, exhaustion, migration, and mitochondrial content. MMCs displayed a distinct immune landscape compared to PBMCs, enriched with tissue-resident NK cells, macrophages, and dendritic cells, alongside changes in mitochondrial mass for various cell subsets and other markers such as PD-1. These findings support a metabolically active, tissue-adapted immune environment within menstrual fluid, representative of the reproductive tract. Exploratory analyses of MMCs from individuals with endometriosis or PCOS revealed disease-specific trends: for example, mitochondrial mass differed across Tregs, CD4 central memory cells, plasmablasts, and cDC1s, with endometriosis and PCOS exhibiting distinct patterns rather than a uniform “reproductive disorder” phenotype. Although these disease-associated findings did not consistently reach statistical significance due to the small cohort size, they demonstrate the potential of menstrual blood immunoprofiling to uncover biologically meaningful differences across diverse immune cell populations. Together, this study establishes menstrual fluid as a valuable, non-invasive sample for immunological assessment and a promising avenue for future biomarker discovery in reproductive disorders.

## Linked entities

- **Proteins:** PDCD1 (programmed cell death 1)
- **Diseases:** endometriosis (MONDO:0005133), polycystic ovary syndrome (MONDO:0008487), PCOS (MONDO:0008487)

## Full-text entities

- **Genes:** CD14 [NCBI Gene 100620530], IL2RA (interleukin 2 receptor subunit alpha) [NCBI Gene 396814] {aka CD25, IL-2RA}, CD28 [NCBI Gene 100738615], CD27 (CD27 molecule) [NCBI Gene 100520023], CD38 (CD38 molecule) [NCBI Gene 100511702], IL7R (interleukin 7 receptor) [NCBI Gene 100271930] {aka CD127}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, Ptprc (protein tyrosine phosphatase receptor type C) [NCBI Gene 19264] {aka B220, CD45R, Cd45, L-CA, Ly-5, Lyt-4}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, CD4 (CD4 molecule) [NCBI Gene 404704], CCR7 (C-C motif chemokine receptor 7) [NCBI Gene 396663]
- **Diseases:** EM (MESH:C000722498), disorders (MESH:D009358), PCOS (MESH:D011085), immune dysregulation (OMIM:614878), Reproductive disorders (MESH:D060737), Mitochondrial (MESH:D028361), endometriosis (MESH:D004715), infertility (MESH:D007246), Inflammation (MESH:D007249)
- **Chemicals:** BioRender (-), sodium azide (MESH:D019810), CO2 (MESH:D002245), DTT (MESH:D004229), PBS (MESH:D007854)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13019135/full.md

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Source: https://tomesphere.com/paper/PMC13019135