Martin-Leo Hansmann, Sonja Scharf, Patrick Wurzel, Sylvia Hartmann
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引用次数: 0
Abstract
The cellular compartments in the lymph node form dynamic networks, enabling coordinated innate and adaptive immunological responses. This compartmentalization of the lymph node into subcompartments, such as the T and B zones, has been proven to be beneficial. The study of lymph node microarchitecture has yielded new insights into a range of fields, including anatomy, pathology and biological processes. This review focuses on three dimensional (D) and 4D investigations of human lymph nodes, with a particular emphasis on comparisons with data obtained from mice. It will discuss the findings of 3D/4D investigations of human lymph nodes. The investigation of the immune system in 3D space and time offers numerous advantages over the analysis of thin tissue sections. It provides data that is not visible in 2D representations. A comparison of volumes, surfaces, cell speeds, cell contact numbers, contact duration times, morphologies and other variables can be made in the context of immune responses and lymphomas. The evaluation of data, the application of statistics and the use of machine learning have all been demonstrated to be valuable. In conditions of reactivity and neoplasia, T cells are the fastest-moving cells. In contrast, B cells show slower movement and higher turning angles in reactive lymphoid tissue and lymphomas. Even slower than B cells are reticulum cells, like follicular dendritic reticulum cells (FDC) of the B zones and macrophages. Fast T cells are especially found in Hodgkin lymphomas and mantle cell lymphomas. Contact times between T and B cells differ between different lymphoma types and may prove useful in defining lymphomas. 4D technologies, which evaluate living tissue slices, are suitable for use in testing checkpoint blockers (such as nivolumab) and other therapeutic drugs or cells. Following incubation with nivolumab, the duration of contacts between CD4-positive T cells and CD30-positive Hodgkin-Reed-Sternberg cells was documented. The preliminary data indicate that 3D and 4D experiments in hematopathology may facilitate new insights into diagnostics, biology, and clinical applications, including the development of new lymphoma classifications.
淋巴结中的细胞区形成动态网络,使先天性和适应性免疫反应得以协调。将淋巴结划分为 T 区和 B 区等亚区已被证明是有益的。对淋巴结微结构的研究为解剖学、病理学和生物过程等一系列领域提供了新的见解。本综述侧重于人体淋巴结的三维(D)和四维研究,特别强调与小鼠数据的比较。它将讨论人体淋巴结的三维/四维研究结果。与薄组织切片分析相比,三维空间和时间的免疫系统研究具有许多优势。它能提供二维图像无法显示的数据。在免疫反应和淋巴瘤的背景下,可以对体积、表面、细胞速度、细胞接触数量、接触持续时间、形态和其他变量进行比较。数据评估、统计应用和机器学习的使用都被证明是非常有价值的。在反应和肿瘤发生的情况下,T 细胞是移动最快的细胞。相反,在反应性淋巴组织和淋巴瘤中,B 细胞的移动速度较慢,转角较大。比 B 细胞更慢的是网状细胞,如 B 区的滤泡树突状网状细胞(FDC)和巨噬细胞。快速 T 细胞尤其见于霍奇金淋巴瘤和套细胞淋巴瘤。不同类型淋巴瘤的 T 细胞和 B 细胞之间的接触时间不同,这可能有助于确定淋巴瘤。4D 技术可对活体组织切片进行评估,适合用于检测检查点阻断剂(如 nivolumab)和其他治疗药物或细胞。在使用 nivolumab 培养后,CD4 阳性 T 细胞和 CD30 阳性霍奇金-瑞德-斯登堡细胞之间的接触持续时间被记录下来。初步数据表明,血液病理学中的三维和四维实验可促进对诊断学、生物学和临床应用的新认识,包括开发新的淋巴瘤分类。
期刊介绍:
Human Pathology is designed to bring information of clinicopathologic significance to human disease to the laboratory and clinical physician. It presents information drawn from morphologic and clinical laboratory studies with direct relevance to the understanding of human diseases. Papers published concern morphologic and clinicopathologic observations, reviews of diseases, analyses of problems in pathology, significant collections of case material and advances in concepts or techniques of value in the analysis and diagnosis of disease. Theoretical and experimental pathology and molecular biology pertinent to human disease are included. This critical journal is well illustrated with exceptional reproductions of photomicrographs and microscopic anatomy.