Department of Pathology and Microbiology, Division of Oncologic Pathology, Nihon University School of Medicine.
Planning, Molecular Diagnostics.
Appl Immunohistochem Mol Morphol. 2021 Feb 1;29(2):118-126. doi: 10.1097/PAI.0000000000000859.
The conversion of immunohistochemical (IHC) results from 3-dimensional tissue to a 2-dimensional visual image without considering tissue thickness poses a considerable risk of misleading IHC intensities. The present study aimed to clarify whether tissue thickness interferes with the estimation of IHC staining intensity and to introduce a control system to manage it.
We prepared cell lines that are used as controls for human epidermal growth factor receptor 2 (HER2) IHC (MDA-MB-231, MDA-MB-175VII, MDA-MV-453, and SK-BR-3), a polyclonal antibody for HER2, an interferometry to measure the tissue thickness of formalin-fixed paraffin-embedded sections, a microscope with a Halogen or an LED light source, a complementary metal-oxide semiconductor camera in which the output signal can be corrected to γ=1, and a program to estimate color elements (hue, saturation, and luminance). It was examined whether tissue thickness interferes with the experimental scoring systems and practical classification of the routine HER2 scoring system.
A noncellular control was shown to be better than a cellular control for managing tissue thickness. The IHC intensity for HER2 was correlated with tissue thickness (R2=0.8094), even under the less-standardized condition, but this correlation was better under the improved standardized condition using corrected γ=1 (R2=0.9282). Discrepancies in practical HER2 scores were increased in sections with thicknesses <2 and >5 μm. A control system to manage tissue thickness was introduced.
Tissue thickness interferes with the estimation of the IHC intensity of HER2 in both experimental and practical scoring systems. A control system for managing tissue thickness is essential to increase the benefits of IHC as a standardized assay for clinical applications.
将 3 维组织的免疫组化(IHC)结果转换为 2 维可视化图像,而不考虑组织厚度,会极大地增加对 IHC 强度的错误判断风险。本研究旨在明确组织厚度是否会干扰 IHC 染色强度的评估,并引入一个控制系统来进行管理。
我们制备了人表皮生长因子受体 2(HER2)IHC 的细胞系作为对照(MDA-MB-231、MDA-MB-175VII、MDA-MV-453 和 SK-BR-3)、HER2 的多克隆抗体、干涉仪来测量福尔马林固定石蜡包埋切片的组织厚度、带有卤素或 LED 光源的显微镜、γ=1 可进行输出信号校正的互补金属氧化物半导体相机,以及一个用于估计颜色元素(色调、饱和度和亮度)的程序。我们检查了组织厚度是否会干扰实验评分系统和常规 HER2 评分系统的实际分类。
与细胞对照相比,非细胞对照更适合用于管理组织厚度。HER2 的 IHC 强度与组织厚度相关(R2=0.8094),即使在标准化程度较低的情况下,但是在使用校正γ=1 的改良标准化条件下,这种相关性更好(R2=0.9282)。厚度<2 μm 和>5 μm 的切片中,实际 HER2 评分的差异增加。引入了一个用于管理组织厚度的控制系统。
组织厚度会干扰实验和实际评分系统中 HER2 的 IHC 强度评估。管理组织厚度的控制系统对于增加 IHC 作为临床应用的标准化检测方法的益处至关重要。