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基质 CD4 (+) T 细胞亚群介导人结直肠癌中的抗肿瘤细胞毒性免疫应答

英文原题:Stromal CD4 (+) T Cell Subsets Mediate Antitumor Cytotoxic Immune Responses in Human Colorectal Carcinoma.

查看英文原题

Stromal CD4 (+) T Cell Subsets Mediate Antitumor Cytotoxic Immune Responses in Human Colorectal Carcinoma.

PubMed 2024/09/01(内容时间) Anticancer Res Q4 · IF 1.8(JCR 2025)

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研究概要

间质 CD4 (+) TIL 亚群需要达到足够的浸润程度,瘤内 CD45RO (+) TIL 才能对癌细胞发挥毒性作用。

中文摘要

使用手术切除的结直肠癌标本进行多重荧光标记,研究具有细胞毒性的CD45RO阳性TIL及依据特征性转录因子表达识别的CD4阳性TIL亚群的浸润。

在整个观察视野或基质区内,CD45RO阳性TIL浸润程度与预后无关。然而,肿瘤巢(肿瘤内区域)中浸润程度较高与良好预后显著相关。CD4阳性TIL及其亚群与预后无关。但分层分析显示,基质CD4阳性TIL及其Th1、Th2、Th17和调节性T细胞亚群浸润程度较高,是肿瘤内CD45RO阳性TIL浸润较高与良好预后相关的必要条件。

基质区CD4阳性TIL亚群需充分浸润,肿瘤内CD45RO阳性TIL才能发挥杀伤癌细胞的作用。这凸显了基质免疫反应对于实现肿瘤内有效细胞毒免疫反应的重要性,也表明TIL空间分布模式对其发挥功能至关重要。

展开英文摘要原文

Multiplex fluorescent labeling was performed using surgically resected colorectal cancer specimens to investigate the infiltration of CD45RO (+) TILs, which exhibit cytotoxicity, and subsets of CD4 (+) TILs, identified by their characteristic transcription factor expression.

The degree of CD45RO (+) TIL infiltration in the entire observation field or stromal area was not associated with prognosis. However, a high degree of infiltration in the tumor nest (intratumoral area) was significantly associated with a favorable prognosis. CD4 (+) TILs and their subsets were not associated with prognosis. However, stratified analyses revealed that a high degree of infiltration of stromal CD4 (+) TILs and the subsets T helper (Th)1, Th2, Th17, and regulatory T cells is necessary for the association between high intratumoral CD45RO (+) TIL infiltration and favorable prognosis.

A sufficient degree of infiltration of stromal CD4 (+) TIL subsets is required for intratumoral CD45RO (+) TILs to exert toxicity against cancer cells. This highlights the significance of stromal immune reactions in achieving effective cytotoxic immune responses in the intratumoral area and demonstrates the critical role of the spatial distribution pattern of TILs in exerting their functions.

论文信息

作者
Fukushima G、Sato E、Udo R、Tago T、Kasahara K、Mazaki J、Iwasaki K、Enomoto M
第一作者单位
Department of Gastrointestinal and Pediatric Surgery, Tokyo Medical University, Tokyo, Japan.Japan
通讯作者单位
Department of Pathology, Institute of Medical Science, Tokyo Medical University, Tokyo, Japan sato-e@tokyo-med.ac.jp.Japan
期刊
Anticancer research2024 Sep
原文标识
PubMed 39197911 · DOI 10.21873/anticanres.17217