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Automated Vibratome Sectioning of Agarose-Embedded Lung Tissue for Multiplex Fluorescence Imaging
Published on: October 6, 2023
Site- and size-dependent differences in pulmonary lymphocyte aggregates: an immunohistochemical and morphometric
Masaya Aoki1, Zhe-Wu Jin2, Go Kamimura1
1Department of General Thoracic Surgery, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.
Anatomy & Cell Biology
|August 12, 2026
Summary
Pulmonary lymphoid aggregates show distinct T- and B-lymphocyte compositions based on location and size. Small aggregates near arterioles are T-lymphocyte-rich, potentially developing into larger, B-cell-containing structures.
Area of Science:
- Pulmonary immunology
- Cellular immunology
- Respiratory pathology
Background:
- Pulmonary lymphoid aggregates are key in chronic lung diseases.
- The predominant lymphocyte type (T or B) in non-tumorous peripheral lung aggregates is unclear.
- Understanding aggregate composition is crucial for local immune response insights.
Purpose of the Study:
- To determine site- and size-dependent patterns of lymphocyte composition in pulmonary aggregates.
- To investigate the ratio of T-lymphocytes to B-lymphocytes in different aggregate types.
- To explore the developmental stages of pulmonary lymphoid aggregates.
Main Methods:
- Immunohistochemical analysis of 138 lymphocyte aggregates from 20 peripheral lung tissue samples.
- Quantification of CD4-positive T-lymphocytes and CD20-positive B-lymphocytes.
- Comparison of lymphocyte ratios (T/B ratio) with aggregate size and location (arteriole-associated, subpleural, bronchiole-associated).
Main Results:
- Arteriole-associated aggregates were small and T-lymphocyte-rich (T/B ratio 3.0-129.2).
- Subpleural and bronchiole-associated aggregates were larger and had lower T/B ratios (0.3-19.8 and 0.2-32.1, respectively).
- Aggregate size weakly correlated with T/B ratio in small arteriole-associated aggregates.
- Podoplanin-positive stromal cells were common; dendritic cells were rare.
Conclusions:
- Pulmonary lymphoid aggregates exhibit site-specific lymphocyte compositions.
- Small, T-lymphocyte-rich aggregates may represent an early stage of development.
- Larger aggregates can evolve into nodular structures with B-cell clusters, suggesting a developmental pathway.

