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Comparative analyses of immune cells and alpha-smooth muscle actin-positive cells under the immunological microenvironment between with and without dense fibrosis in primary central nervous system lymphoma.

Authors :
Takei J
Maeda M
Fukasawa N
Kawashima M
Miyake M
Tomoto K
Nawate S
Teshigawara A
Suzuki T
Yamamoto Y
Nagashima H
Mori R
Fukushima R
Matsushima S
Kino H
Muroi A
Tsurubuchi T
Sakamoto N
Nishiwaki K
Yano S
Hasegawa Y
Murayama Y
Akasaki Y
Shimoda M
Ishikawa E
Tanaka T
Source :
Brain tumor pathology [Brain Tumor Pathol] 2024 Oct; Vol. 41 (3-4), pp. 97-108. Date of Electronic Publication: 2024 Aug 26.
Publication Year :
2024

Abstract

Histopathologic examinations of primary central nervous system lymphoma (PCNSL) reveal concentric accumulation of lymphocytes in the perivascular area with fibrosis. However, the nature of this fibrosis in "stiff" PCNSL remains unclear. We have encountered some PCNSLs with hard masses as surgical findings. This study investigated the dense fibrous status and tumor microenvironment of PCNSLs with or without stiffness. We evaluated by silver-impregnation nine PCNSLs with stiffness and 26 PCNSLs without stiffness. Six of the nine stiff PCNSLs showed pathological features of prominent fibrosis characterized by aggregation of reticulin fibers, and collagen accumulations. Alpha-smooth muscle actin (αSMA)-positive spindle cells as a cancer-associated fibroblast, the populations of T lymphocytes, and macrophages were compared between fibrous and control PCNSLs. Fibrous PCNSLs included abundant αSMA-positive cells in both intra- and extra-tumor environments (5/6, 87% and 3/6, 50%, respectively). Conversely, only one out of the seven control PCNSL contained αSMA-positive cells in the intra-tumoral area. Furthermore, the presence of extra-tumoral αSMA-positive cells was associated with infiltration of T lymphocytes and macrophages. In conclusion, recognizing the presence of dense fibrosis in PCNSL can provide insights into the tumor microenvironment. These results may help stratify patients with PCNSL and improve immunotherapies for these patients.<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
1861-387X
Volume :
41
Issue :
3-4
Database :
MEDLINE
Journal :
Brain tumor pathology
Publication Type :
Academic Journal
Accession number :
39186169
Full Text :
https://doi.org/10.1007/s10014-024-00488-7