CD20+和CD204+在胸膜上皮瘤中表现出明显的预后关联
Qinyang Chen1, Jian Zhang1, Jianwei Feng2
1The Academy of Chinese Health Risks, West China Hospital, Sichuan University, Chengdu, China.
Frontiers in oncology
|December 4, 2025
概括
瘤透免疫细胞 (TIIC) 影响胸膜上皮瘤 (TETs) 的存活率. 高CD20+ TIIC改善了结果,而CD204+ TIIC表明预后较差,这表明M2巨细胞向更好的TETs治疗.
科学领域:
- 在瘤学瘤学.
- 免疫学 免疫学 免疫学
- 病理学 病理学 病理学
背景情况:
- 甲状腺上皮瘤 (TETs) 是甲状腺的罕见癌症.
- 瘤微环境 (TME) 和其免疫细胞对癌症进展至关重要.
- 在TET中了解瘤透免疫细胞 (TIIC) 可以揭示预后标志物.
研究的目的:
- 在TET中描述TIIC.
- 评估TIIC在TETs的TME中的预后意义.
- 在TETs中识别与无病生存率 (DFS) 和总生存率 (OS) 相关的免疫标志物.
主要方法:
- 125个手术切除的TET (2009-2021) 的回顾性分析.
- 免疫组织化学染色以评估TIIC分布.
- 考克斯回归分析用于评估免疫标记物与生存结果之间的关联.
主要成果:
- CD20,CD204,CD206和CD47是DFS的潜在预测因素.
- CD20和CD204显示出对OS的预后相关性.
- 较高的 stromal CD20+ TIIC 密度与延长的 DFS 和 OS 相关联.
- 增加的CD204+TIIC透与减少的DFS和OS有关.
结论:
- 特定的TIIC子集,包括CD20+和CD204+细胞,在TET中具有显著的预后价值.
- CD20+ TIIC与更好的生存率有关,而CD204+ TIIC表明预后更差.
- 针对M2巨驱动的免疫抑制可能是TETs的一个有希望的治疗策略.
更多相关视频
07:32Author Spotlight: Investigating Immune Cell Dynamics in the Tumor Microenvironment — Challenges and Innovations in Cancer Prognosis
Published on: April 12, 2024
1.9K
09:32Multiplexed Immunofluorescence Analysis and Quantification of Intratumoral PD-1+ Tim-3+ CD8+ T Cells
Published on: February 8, 2018
15.3K
相关概念视频
T Cell Activation and Clonal Selection
14.6K
T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
Naive T cells that have not yet encountered an antigen express two primary CD...
Naive T cells that have not yet encountered an antigen express two primary CD...
14.6K
T Cell Types and Functions
2.1K
When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
2.1K
