# A Paired Flow Cytometry–Pathology Assessment for Immune Cell Detection in Intestinal Biopsies: Proof of Principle

**Authors:** Alexandros Skamnelos, Georgios S. Markopoulos, Lefkothea Dova, Ioulia Tragani, Meropi Katsipaneli, Dimitrios Christodoulou, Konstantinos Katsanos, Evangeli Lampri

PMC · DOI: 10.3390/mps8050122 · Methods and Protocols · 2025-10-16

## TL;DR

This study shows how combining flow cytometry and pathology can accurately count immune cells in intestinal biopsies.

## Contribution

A new integrated workflow combining flow cytometry and pathology for immune cell quantification in limited biopsy samples is proposed.

## Key findings

- A pilot analysis of 10 samples showed high concordance between flow cytometry and pathology results.
- The combined approach allows cross-validation between methods, improving diagnostic accuracy.
- The workflow is feasible for immune cell assessment in intestinal biopsies with limited material.

## Abstract

Accurate quantification of immune cell subpopulations is essential for understanding immune responses in research and clinical settings. Flow cytometry (FC) is widely used for immune cell phenotyping, providing rapid and quantitative single-cell resolution. However, tissue-based pathological assessment offers additional spatial and morphological context that is often necessary for a comprehensive understanding of immune cell distribution. Traditionally, these methods are applied separately to different specimens, limiting direct comparative analysis. Here, we describe a simple combined approach to immune cell quantification that integrates both FC and pathology analysis within the same tissue specimen of colon biopsies. Tissue samples were divided into two portions: one processed into a single-cell suspension for FC-based characterization of CD45+, CD3+, CD4+, and CD8+ T cells and another formalin-fixed, paraffin-embedded (FFPE), and analyzed with hematoxylin and eosin (H&E) for eosinophils and immunohistochemistry (IHC) for CD4 and CD8. A pilot analysis of 10 samples shows high concordance of the results taken from the two methods, allowing for cross-validation between methodologies and improved diagnostic accuracy. This proof-of-principle study demonstrates the feasibility of an integrated workflow that combines FC and pathology for immune cell quantification, which provides assessment of immune cell populations from the limited material of intestinal biopsies with potential for improved diagnostic accuracy.

## Linked entities

- **Proteins:** PTPRC (protein tyrosine phosphatase receptor type C), cd.3 (Cd.3 conserved hypothetical protein), CD4 (CD4 molecule), CD8A (CD8 subunit alpha)

## Full-text entities

- **Genes:** CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, PTPRC (protein tyrosine phosphatase receptor type C) [NCBI Gene 5788] {aka B220, CD45, CD45R, GP180, IMD105, L-CA}
- **Chemicals:** paraffin (MESH:D010232)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12566358/full.md

## References

24 references — full list in the complete paper: https://tomesphere.com/paper/PMC12566358/full.md

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Source: https://tomesphere.com/paper/PMC12566358