The differences in the distribution characteristics and prognostic value of tumor-infiltrating T lymphocyte subsets between lung adenocarcinoma and lung squamous cell carcinoma.

IF 2.1 4区 医学 Q3 ONCOLOGY
Zhen Zhang, Shaoyan Zhang, Yalai Xu, Xiaoning Liu, Wenjie Dong
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引用次数: 0

Abstract

Background: The characteristics of tumor immune microenvironment are important factors affecting the efficacy of immunotherapy, and there are differences in the distribution of tumor-infiltrating lymphocyte (TIL) subsets in different types of tumors. This study aims to compare the distributions of cluster of differentiation (CD) 4+ and CD4+ T cell subsets of TILs and their clinical significance between lung adenocarcinoma (LUAD) and lung squamous cell carcinoma (LUSC).

Methods: The tumor tissues of 78 LUAD and 56 LUSC patients who underwent surgery at The Second Affiliated Hospital of Zhengzhou University between October 2020 and October 2022 were collected, TIL level were detected by pathological observation, and the proportions of CD4+, CD4+ T cell subsets and CD4+/CD4+ ratio in TILs were detected by flow cytometry. These indicators were compared between LUAD and LUSC, and their correlations with clinicopathological characteristics and patient survival were analyzed.

Results: There was no significant difference in the TILs level between LUAD and LUSC (P>0.05). The CD4+/CD4+ ratio in LUSC was lower, and proportion of CD4+ T cells was higher than those in LUAD (all P<0.05). In LUAD, the proportions of CD4+, CD4+ T cells and CD4+/CD4+ were correlated with tumor size or tumor-node-metastasis (TNM) stage, while in LUSC, only the proportions of CD4+ and CD4+ T cells were correlated with tumor size, degree of differentiation or TNM stage. In LUAD patients, higher proportions of CD4+, CD4+ T cells and lower CD4+/CD4+ predicted longer survival, and high CD4+/CD4+ (>1.04) was an independent risk factor for PFS and OS (P<0.05); In LUSC patients, there was no correlation between the proportions of CD4+ T cells, CD4+ T cells and CD4+/CD4+ ratio, and patient prognosis (P>0.05).

Conclusions: There were differences in the distribution and balance of CD4+ and CD4+ TIL subsets between LUAD and LUSC, among which CD4/CD4+ ratio closely affected the prognosis of LUAD patients but had relatively weak prognostic value in LUSC patients due to the restriction of CD4+ T cells.

肺腺癌与肺鳞状细胞癌浸润性T淋巴细胞亚群分布特征及预后价值的差异
背景:肿瘤免疫微环境的特征是影响免疫疗法疗效的重要因素:肿瘤免疫微环境的特征是影响免疫疗法疗效的重要因素,而肿瘤浸润淋巴细胞(TIL)亚群在不同类型肿瘤中的分布存在差异。本研究旨在比较肺腺癌(LUAD)和肺鳞癌(LUSC)中TIL的分化簇(CD)4+和CD4+ T细胞亚群的分布及其临床意义:收集2020年10月至2022年10月期间在郑州大学第二附属医院接受手术治疗的78例LUAD和56例LUSC患者的肿瘤组织,通过病理观察检测TIL水平,采用流式细胞术检测TIL中CD4+、CD4+T细胞亚群的比例及CD4+/CD4+比值。比较了LUAD和LUSC的这些指标,并分析了它们与临床病理特征和患者生存期的相关性:结果:LUAD和LUSC的TILs水平无明显差异(P>0.05)。LUSC的CD4+/CD4+比值低于LUAD,CD4+T细胞比例高于LUAD(均为P1.04),是PFS和OS的独立危险因素(P0.05):结论:CD4+和CD4+ TIL亚群的分布和平衡在LUAD和LUSC之间存在差异,其中CD4/CD4+比值对LUAD患者的预后影响很大,但由于CD4+ T细胞的限制,对LUSC患者的预后价值相对较弱。
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来源期刊
CiteScore
3.90
自引率
0.00%
发文量
0
期刊介绍: The Chinese Clinical Oncology (Print ISSN 2304-3865; Online ISSN 2304-3873; Chin Clin Oncol; CCO) publishes articles that describe new findings in the field of oncology, and provides current and practical information on diagnosis, prevention and clinical investigations of cancer. Specific areas of interest include, but are not limited to: multimodality therapy, biomarkers, imaging, tumor biology, pathology, chemoprevention, and technical advances related to cancer. The aim of the Journal is to provide a forum for the dissemination of original research articles as well as review articles in all areas related to cancer. It is an international, peer-reviewed journal with a focus on cutting-edge findings in this rapidly changing field. To that end, Chin Clin Oncol is dedicated to translating the latest research developments into best multimodality practice. The journal features a distinguished editorial board, which brings together a team of highly experienced specialists in cancer treatment and research. The diverse experience of the board members allows our editorial panel to lend their expertise to a broad spectrum of cancer subjects.
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