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  4. Abstract 5257: Functional profiling of γδ T cell subsets in malignant pleural effusion and their prognostic value in advanced lung cancer
 
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Abstract 5257: Functional profiling of γδ T cell subsets in malignant pleural effusion and their prognostic value in advanced lung cancer

Journal
Cancer Research
Journal Volume
85
Journal Issue
8_Supplement_1
Start Page
5257-5257
ISSN
0008-5472
1538-7445
Date Issued
2025-04-21
Author(s)
Shih, Tsai-Tsen
Wu, Yi-Chieh
HSING-CHEN TSAI  
DOI
10.1158/1538-7445.am2025-5257
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/740022
Abstract
The tumor immune microenvironment reflects a patient's immune reserve and offers valuable insights for clinical decision-making. It has the potential to stratify late-stage cancer patients, identifying those likely to benefit from aggressive therapies and those better suited for palliative care. However, obtaining detailed immune profiling from tumor tissues often requires invasive biopsies and poses additional risks. Malignant pleural effusion (MPE), a common complication in advanced lung cancer, provides a minimally invasive alternative for evaluating microenvironmental immune dynamics via thoracentesis. In this study, we analyzed the immune cell composition of malignant pleural effusions (MPE) from 73 patients with late-stage lung adenocarcinoma using high-dimensional spectral flow cytometry and a comprehensive panel of immunophenotypic and functional markers. Our analysis focused on cytotoxic immune cell populations, including NK cells, NKT cells, CD8+ T cells, and γδ T cells. Notably, γδ T cells constituted approximately 1.4% of viable cells, with the Vδ1 and Vδ2 subpopulations representing 32.3% and 46.6% of the γδ T cell compartment, respectively. Higher γδ T cell abundance was associated with shorter overall survival, while no correlation was observed for other immune cell populations. Further analysis revealed that a higher Vδ2/Vδ1 ratio correlated with poorer clinical outcomes. Conversely, elevated expression of the activating receptor DNAM-1 (CD226) on Vδ1 cells was observed in long-term survivors (>2 years) compared to short-term survivors (<6 months), independent of mutation type or treatment modality. These findings were validated using the TCGA lung cancer datasets, confirming a strong link between high DNAM-1 expression and extended survival. In conclusion, γδ T cell subpopulations in MPE, particularly the Vδ1 and Vδ2 subsets, are promising biomarkers for immune fitness and prognosis in advanced lung adenocarcinoma. These results highlight the potential of γδ T cells to identify late-stage patients likely to benefit from aggressive therapies and emphasize the need for larger-scale studies to confirm these findings.
Publisher
American Association for Cancer Research (AACR)
Type
Meeting Abstract

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