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A high density of T-cell lymphocytes and Tregs subset correlate to a worse survival in major salivary gland carcinomas.

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Scientific reports 📖 저널 OA 97.3% 2021: 24/24 OA 2022: 32/32 OA 2023: 45/45 OA 2024: 140/140 OA 2025: 938/938 OA 2026: 715/767 OA 2021~2026 2026 Vol.16(1) OA
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Anconelli D, Vasuri F, Novelli L, Saragoni L, Messerini L, Saieva C

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Salivary gland carcinomas (SGC) are rare and heterogeneous tumors with limited therapeutic options in advanced stages.

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  • p-value p = 0.009
  • p-value p = 0.046

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APA Anconelli D, Vasuri F, et al. (2026). A high density of T-cell lymphocytes and Tregs subset correlate to a worse survival in major salivary gland carcinomas.. Scientific reports, 16(1). https://doi.org/10.1038/s41598-026-39357-y
MLA Anconelli D, et al.. "A high density of T-cell lymphocytes and Tregs subset correlate to a worse survival in major salivary gland carcinomas.." Scientific reports, vol. 16, no. 1, 2026.
PMID 41775752 ↗

Abstract

Salivary gland carcinomas (SGC) are rare and heterogeneous tumors with limited therapeutic options in advanced stages. Recent evidence suggests a potential role of the tumor immune microenvironment (TME) in disease progression. This study aimed to investigate the immune profile of SGCs by analyzing tumor-infiltrating lymphocytes (TILs), tumor-associated macrophages (TAMs), and PD-L1 expression, and to assess their correlation with histological grade and clinical outcome. A retrospective analysis was conducted on 103 SGC cases. Immunohistochemistry for CD3, CD4, CD8, CD20, CD56, PD-1, PD-L1, FOXP3, CD68, and CD163 was performed. Digital slide analysis was carried out in intratumoral and peritumoral regions using QuPath software. High intratumoral FOXP3 + Tregs were significantly associated with high-grade tumors and worse progression-free survival (PFS) (p = 0.009). A higher peritumoral CD3 + T cell density correlated with poor prognosis (p = 0.046). Concordance between pathologist assessments and QuPath quantification was moderate to high (Cohen's K = 0.71). In conclusion, intratumoral Tregs and peritumoural T lymphocytes may be used as negative prognostic biomarkers. Future multicentric studies and AI (Artificial Intelligence)-driven analyses could enhance immune characterization and guide immunotherapeutic strategies in SGC.

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