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Updated: Dec 22, 2025

Multiplexed Immunofluorescence Analysis and Quantification of Intratumoral PD-1+ Tim-3+ CD8+ T Cells
Published on: February 8, 2018
Plasmablastic Lymphomas: Characterization of Tumor Microenvironment Using CD163 and PD-1 Immunohistochemistry.
Janice S Ahn1, Ali Al-Habib2, Jeffrey A Vos1
1Department of Pathology, Anatomy and Laboratory Medicine, West Virginia University, Morgantown, WV, USA.
Plasmablastic lymphoma (PBL) often features abundant tumor-associated macrophages (TAMs) and few tumor-infiltrating lymphocytes (TILs). This TAM-high/TIL-low microenvironment warrants further investigation for PD-1/PD-L1 pathway roles.
Area of Science:
- Oncology
- Immunology
- Pathology
Background:
- Plasmablastic lymphoma (PBL) is an aggressive B-cell neoplasm.
- The tumor microenvironment (TME) significantly influences cancer progression.
- Tumor-associated macrophages (TAMs) and tumor-infiltrating lymphocytes (TILs) are key immune components in the TME.
Purpose of the Study:
- To characterize the TME of PBL by quantifying CD163(+) TAMs and PD1(+) TILs.
- To review the role of the PD-1/PD-L1 pathway in hematopoietic neoplasms.
- To explore potential mechanisms and future research directions.
Main Methods:
- Immunohistochemical analysis of CD163 and PD1 in 11 PBL cases.
- Quantification of positive TAMs and TILs percentages.
- Classification of cases into high/low TAMs and TILs based on established cutoffs (≥30% and >5%, respectively).
Main Results:
- A majority of PBL cases (73%) exhibited high TAMs.
- A minority of cases (27%) showed high TILs.
- A trend towards negative correlation between TAMs and TILs (p=0.08) was observed, with a predominant TAM-high/TIL-low pattern (63%).
Conclusions:
- PBL TME typically shows high TAMs and low TILs.
- Further studies are needed to clarify the clinical significance of TILs and the impact of EBV/HIV.
- Investigating PD-L1 expression in PBL is warranted due to its association with TAMs in other malignancies.
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