Abstract | BACKGROUND: MATERIALS AND METHODS: RESULTS: Tumor-infiltrating lymphocyte (TIL) infiltration could be observed in the majority of the investigated specimens (CD3+: 66/74 (89.2%); CD8+: 47/74 (63.5%); CD45RO+: 29/73 (39.2%); FOXP3+ 19/74 (25.7%); PD1+: 3/74 (4.1%). No difference in TIL infiltration was observed between SFT/HPC and meningioma cases. Higher density of FOXP3+ TILs was observed with increasing WHO grade in meningioma specimens (p = 0.005). Membranous programmed cell death ligand 1 (PD-L1) expression was observed in 4/74 (5.4%) specimens, with 3/74 (4.1%) presenting with 1% and 1/74 (1.4%) with 3% PD-L1 expressing tumor cells. Lymphatic vessels as identified by podoplanin immunohistochemistry were observed in 10/74 (13.5%) specimens and were significantly associated with presence of membranous PD-L1 expression on tumor cells (p = 0.003). CONCLUSION: Infiltration by various TIL subtypes can be observed in the majority of meningeal neoplasms, with enrichment of FOXP3-positive regulatory T-cells in higher-grade meningioma. PD-L1 expression on tumor cells was only infrequently found. A better understanding of the pathobiological role of the immune system in meningeal neoplasms may facilitate development of immunomodulatory treatment approaches in meningeal tumors.
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Authors | Anna Sophie Berghoff, Philip Kresl, Orsolya Rajky, Georg Widhalm, Gerda Ricken, Johannes A Hainfellner, Christine Marosi, Peter Birner, Matthias Preusser |
Journal | Clinical neuropathology
(Clin Neuropathol)
2020 Nov/Dec
Vol. 39
Issue 6
Pg. 256-262
ISSN: 0722-5091 [Print] Germany |
PMID | 32831157
(Publication Type: Journal Article)
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Chemical References |
- B7-H1 Antigen
- Biomarkers, Tumor
- FOXP3 protein, human
- Forkhead Transcription Factors
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Topics |
- Adult
- Aged
- B7-H1 Antigen
(metabolism)
- Biomarkers, Tumor
(analysis)
- Forkhead Transcription Factors
(metabolism)
- Hemangiopericytoma
(immunology, pathology)
- Humans
- Lymphocytes, Tumor-Infiltrating
(immunology, metabolism, pathology)
- Male
- Meningeal Neoplasms
(immunology, pathology)
- Meningioma
(immunology, pathology)
- Middle Aged
- Solitary Fibrous Tumors
(pathology)
- Tumor Microenvironment
(immunology)
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