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High PTX3 expression is associated with a poor prognosis in diffuse large B-cell lymphoma
Joaquim Carreras1, Yara Yukie Kikuti1, Shinichiro Hiraiwa1
1Department of Pathology, School of Medicine, Tokai University, Isehara, Japan.
Cancer Science
|October 27, 2021
Summary
High infiltration of M2c-like macrophages and low regulatory T lymphocytes (Tregs) in diffuse large B-cell lymphoma (DLBCL) indicates poor prognosis. Pentraxin 3 (PTX3) is identified as a novel prognostic biomarker for DLBCL patient outcomes.
Area of Science:
- Immunology
- Oncology
- Pathology
Background:
- Tumor-associated macrophages (TAMs) are linked to poor prognosis in diffuse large B-cell lymphoma (DLBCL).
- Macrophage heterogeneity and polarization in DLBCL require further investigation for their pathological roles.
Purpose of the Study:
- To characterize the tumor microenvironment in DLBCL, focusing on macrophage infiltration and immune cell polarization.
- To identify novel prognostic biomarkers for DLBCL, particularly related to immune cell subsets.
Main Methods:
- Immunohistochemistry was used to analyze macrophage and T cell infiltration in a training set (132 cases) and validation set (159 cases) of DLBCL.
- Gene expression profiling was performed on a subset of cases to analyze immune-related pathways.
- Statistical analyses, including multivariate analysis, were conducted to determine prognostic relevance.
Main Results:
- High infiltration of CD163 and pentraxin 3 (PTX3)-positive macrophages (M2c-like) and low infiltration of FOXP3-positive regulatory T lymphocytes (Tregs) correlated with poor DLBCL survival.
- PTX3 was identified as a significant independent prognostic variable in multivariate analysis.
- Gene expression analysis in high PTX3 cases revealed upregulation of immune response and macrophage-related pathways.
Conclusions:
- High infiltration of M2c-like macrophages and low infiltration of Tregs are associated with a poor prognosis in DLBCL.
- Pentraxin 3 (PTX3) is a novel and significant prognostic biomarker for DLBCL, reflecting immune microenvironment alterations.

