← 返回

使用图像分析软件的 CD8 和 PD-1 阳性 T 细胞自动测量方法开发

英文原题:Development of an Automatic Measurement Method for CD8 and PD-1 Positive T Cells Using Image Analysis Software.

查看英文原题

Development of an Automatic Measurement Method for CD8 and PD-1 Positive T Cells Using Image Analysis Software.

PubMed 2022/01/01(内容时间) Anticancer Res Q4 · IF 1.8(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

研究概要

基于影像软件的自动测量可能是一种简单且有用的工具,用于从 TIL 状态方面评估癌症免疫疗法的治疗效果。

研究思路结论见上方概要

随着使用免疫检查点阻断(ICB)疗法的癌症免疫治疗的进展,需要使用成像分析软件对TIL(肿瘤浸润淋巴细胞)状态进行组织学观察,以评估ICB的抗肿瘤效果。

从结直肠癌和胃癌患者中获取的福尔马林固定石蜡包埋切片,这些患者具有超过500个单核苷酸变异,用抗CD8和抗PD-1抗体进行染色。基于我们自己的算法和成像分析软件,建立了一种自动TIL测量方法,并与人工计数方法进行了比较。

在CD8+ T细胞计数中,手动和自动计数方法之间存在良好的相关性(Pearson检验r=0.738)。然而,在PD-1+T细胞测量中,两组的TIL数量存在较大差异。调整参数设置后,PD-1+T细胞测量中手动和自动方法之间的相关性有所改善(Pearson检验r=0.668)。

展开英文摘要原文

Formalin-fixed paraffin-embedded sections obtained from colorectal cancer and gastric cancer patients with more than 500 single nucleotide variants were stained with anti-CD8 and anti-PD-1 antibodies. Based on our own algorithm and imaging analysis software, an automatic TIL measurement method was established and compared to the manual counting methods.

In the CD8 + T cell number measurement, there was a good correlation (r=0.738 by Pearson test) between the manual and automated counting methods. However, in the PD-1 + T cell measurement, there was a large difference in TIL numbers in both groups. After adjustment of the parameter settings, the correlation between the manual and automated methods in the PD-1 + T cell measurements improved (r=0.668 by Pearson test).

An imaging software-based automatic measurement could be a simple and useful tool for evaluating the therapeutic effect of cancer immunotherapies in terms of TIL status.

论文信息

作者
Miyata H、Akiyama Y、Iizuka A、Kondou R、Maeda C、Kanematsu A、Watanabe K、Ashizawa T
第一作者单位
Immunotherapy Division, Shizuoka Cancer Center Research Institute, Shizuoka, Japan.Japan
通讯作者单位
Immunotherapy Division, Shizuoka Cancer Center Research Institute, Shizuoka, Japan y.akiyama@scchr.jp.Japan
期刊
Anticancer research2022 Jan
原文标识
PubMed 34969752 · DOI 10.21873/anticanres.15500