# Single-particle analysis of small extracellular vesicles from human follicular fluid unveils immunomodulatory PD-L1+ subpopulations and potentially fertility biomarkers

**Authors:** Barbara Bortot, Roberta Di Florio, Gabriella Zito, Francesco Valle, Marco Brucale, Giuseppe Ricci, Paola Vigano, Stefania Biffi

PMC · DOI: 10.7717/peerj.20057 · PeerJ · 2025-10-28

## TL;DR

This study identifies small extracellular vesicles with PD-L1 in human follicular fluid, which may help regulate immune responses and serve as fertility biomarkers.

## Contribution

The study reveals a distinct PD-L1+ subpopulation of small extracellular vesicles in follicular fluid with potential immunomodulatory roles.

## Key findings

- Most tetraspanin-expressing extracellular vesicles in follicular fluid are smaller than 50 nm.
- PD-L1 shows preferential co-expression with CD9+ vesicles and is most consistently expressed across patients.
- PD-L1+ vesicles may act as biomarkers for immune regulation in reproductive treatments.

## Abstract

In certain cell systems, small extracellular vesicles bearing PD-L1 (PD-L1+ sEVs) have been shown to suppress T-cell immunity. We investigated whether a distinct profile of PD-L1+ sEVs exists in human follicular fluid (FF), a microenvironment where immune tolerance is crucial for proper follicular development. We characterized the expression and colocalization of CD63, CD81, CD9, and PD-L1 in sEVs derived from FF of women undergoing fertility treatments (n = 10), utilizing single-particle interferometric reflectance imaging sensing combined with single-particle antibody capture and immunofluorescence labeling. Additionally, sEV size distribution was analysed via atomic force microscopy. These integrated techniques revealed that the majority of tetraspanin-expressing EVs in human FF are smaller than 50 nm. Statistical analysis revealed a significant difference in PD-L1 co-expression across CD63, CD81, and CD9, confirming a preferential association of PD-L1 with CD9+ sEVs. Coefficients of variation across the cohort further indicated that PD-L1/CD9 co-expression was the most consistent among patients, suggesting a stable and distinct sEV subpopulation. These findings underscore the potential of PD-L1+ sEVs as biomarkers for immune regulation in reproductive treatments. The discovery of distinct PD-L1+ sEV subpopulations suggests a role in modulating immune responses within the follicular microenvironment. Further studies are warranted to investigate the functional relevance of these vesicles in predicting fertility outcome, promoting local immune tolerance, and facilitating follicular development.

## Linked entities

- **Genes:** CD274 (CD274 molecule) [NCBI Gene 29126], CD63 (CD63 molecule) [NCBI Gene 967], CD81 (CD81 molecule) [NCBI Gene 975], CD9 (CD9 molecule) [NCBI Gene 928]
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** CD81 (CD81 molecule) [NCBI Gene 975] {aka CVID6, S5.7, TAPA1, TSPAN28}, CD63 (CD63 molecule) [NCBI Gene 967] {aka AD1, HOP-26, ME491, MLA1, OMA81H, Pltgp40}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, CD9 (CD9 molecule) [NCBI Gene 928] {aka BTCC-1, DRAP-27, MIC3, MRP-1, TSPAN-29, TSPAN29}
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12577570/full.md

## References

54 references — full list in the complete paper: https://tomesphere.com/paper/PMC12577570/full.md

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Source: https://tomesphere.com/paper/PMC12577570