Abstract

This study deals with 3D laser investigation on the border between the human lymph node T-zone and germinal centre. Only a few T-cells specific for antigen selected B-cells are allowed to enter germinal centres. This selection process is guided by sinus structures, chemokine gradients and inherent motility of the lymphoid cells. We measured gaps and wall-like structures manually, using IMARIS, a 3D image software for analysis and interpretation of microscopy datasets. In this paper, we describe alpha-actin positive and semipermeable walls and wall-like structures that may hinder T-cells and other cell types from entering germinal centres. Some clearly defined holes or gaps probably regulate lymphoid traffic between T- and B-cell areas. In lymphadenitis, the morphology of this border structure is clearly defined. However, in case of malignant lymphoma, the wall-like structure is disrupted. This has been demonstrated exemplarily in case of angioimmunoblastic T-cell lymphoma. We revealed significant differences of lengths of the wall-like structures in angioimmunoblastic T-cell lymphoma in comparison with wall-like structures in reactive tissue slices. The alterations of morphological structures lead to abnormal and less controlled T- and B-cell distributions probably preventing the immune defence against tumour cells and infectious agents by dysregulating immune homeostasis.

Highlights

  • The human immune system is decentralised and includes about 300 to 700 lymph nodes

  • We found alpha-actin expressing fibroblastic reticular cells (FRC) walls (Fig 1) providing a defined compartmentalisation of the B-/T-zone

  • Tissue staining for BCL6 and IgD displays that the FRC walls compartmentalise germinal centre (GC) including the follicular mantle

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Summary

Introduction

Each lymph node drains a special peripheral area and is divided into compartments, such as a T-, as well as a B-zone. Both compartments feature different specialized networks of reticular cells, which guide the lymphocyte movement. The B-cell compartments show a network of follicular dendritic reticulum cells (FDC) enabling the germinal centre’s (GC) cell reactions [1, 2]. This investigation focuses on the T-cell compartments consisting of fibroblastic reticular cells (FRC), forming sinus structures.

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