# Expression of immunophenotypic markers in blood mononuclear cells of patients with advanced head and neck squamous cells carcinoma

**Authors:** Adriana Torres da Silva, Érica Leandro Marciano Vieira, Ana Cristina Simões e Silva, Andy Petroianu

PMC · DOI: 10.1590/acb405425 · Acta Cirúrgica Brasileira · 2025-08-08

## TL;DR

This study compares immune cell markers in cancer patients and healthy individuals, finding changes in T and B cells that could serve as biomarkers.

## Contribution

The study identifies specific immunophenotypic changes in PBMCs of HNSCC patients that may act as potential biomarkers.

## Key findings

- HNSCC patients had increased CD3+CD4+ T lymphocytes and NK cells compared to healthy volunteers.
- CD8 T cells were decreased in HNSCC patients.
- CD69 activation marker was elevated on T and B cells in cancer patients.

## Abstract

To evaluate peripheral blood mononuclear cells (PBMCs) from patients with advanced head and neck squamous cell carcinoma (HNSCC) in comparison with healthy volunteers, as they can be potential biomarkers.

Immunophenotyping was performed using flow cytometry of blood mononuclear cells from two groups of adult men: group 1 (n = 14), diagnosed with HNSCC (mouth, larynx, and hypopharynx); and group 2 (n = 14), volunteers, healthy, and without the use of drugs. The cell groups studied were T lymphocytes (CD3, CD4, CD8, CD56 and CD69), B lymphocytes (CD19, CD69), neutrophils (CD11a, CD16, CD66b, HLA-DR), and monocytes (CD14, CD86).

In group 1, there were an increase in CD3+CD4+ T lymphocytes (p < 0.001) and NK 56+ cells (p = 0.009) and a decrease in CD3+CD8+ T lymphocytes (p = 0.02) in comparison with group 2. In patients with HNSCC, an increase was found in the expression of the CD69 marker in CD3+CD4+ T lymphocytes (p = 0.03) and CD19+ B lymphocytes (p = 0.01) when compared to healthy volunteers.

HNSCC triggers a systemic inflammatory response with a decrease in CD8 T cells and an increase in CD4 T and CD56 natural killer cells. CD69 early activation marker was expressed by T and B cells.

## Linked entities

- **Proteins:** cd.3 (Cd.3 conserved hypothetical protein), CD4 (CD4 molecule), CD8A (CD8 subunit alpha), NCAM1 (neural cell adhesion molecule 1), CD69 (CD69 molecule), CD19 (CD19 molecule), ITGAL (integrin subunit alpha L), FCGR3B (Fc gamma receptor IIIb), CEACAM8 (CEA cell adhesion molecule 8), CD14 (CD14 molecule), CD86 (CD86 molecule)
- **Diseases:** head and neck squamous cell carcinoma (MONDO:0010150), HNSCC (MONDO:0010150)

## Full-text entities

- **Genes:** FCGR3A (Fc gamma receptor IIIa) [NCBI Gene 2214] {aka CD16-II, CD16A, FCG3, FCGR3, FCRIIIA, FcGRIIIA}, ITGAL (integrin subunit alpha L) [NCBI Gene 3683] {aka CD11A, EV6, HNA-5, LFA-1, LFA1A}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, CEACAM8 (CEA cell adhesion molecule 8) [NCBI Gene 1088] {aka CD66b, CD67, CGM6, NCA-95}, CD19 (CD19 molecule) [NCBI Gene 930] {aka B4, CVID3}, CD86 (CD86 molecule) [NCBI Gene 942] {aka B7-2, B7.2, B70, BU63, CD28LG2, CD86 v6}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CD14 (CD14 molecule) [NCBI Gene 929], CD69 (CD69 molecule) [NCBI Gene 969] {aka AIM, BL-AC/P26, CLEC2C, EA1, GP32/28, MLR-3}, NCAM1 (neural cell adhesion molecule 1) [NCBI Gene 4684] {aka CD56, MSK39, NCAM}
- **Diseases:** HNSCC (MESH:D000077195), inflammatory (MESH:D007249)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12333569/full.md

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Source: https://tomesphere.com/paper/PMC12333569