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Updated: May 10, 2026

Isolation and Flow Cytometric Analysis of Glioma-infiltrating Peripheral Blood Mononuclear Cells
Published on: November 28, 2015
Circulating microparticles of glial origin and tissue factor bearing in high-grade glioma: a potential prothrombotic
Maria Teresa Sartori1, Alessandro Della Puppa, Andrea Ballin
1Department of Cardiologic, Thoracic and Vascular Sciences, via Giustiniani 2, Padua, Italy. mtsart@unipd.it
Abstract:
Venous thromboembolism (VTE) may complicate the clinical course of glioblastoma multiforme (GBM). Circulating microparticles (MPs) have been associated with cancer-related VTE. Sixty-one consecutive patients with GBM undergoing gross-total (41) or subtotal (20) surgical resection followed by radio-chemotherapy were prospectively evaluated. MPs numbers according to cellular origin and the procoagulant activity of annexin V positive (AV+) MPs (MP-activity) were measured before surgery and then 1 week and 1, 4, and 7 months after surgery. Glial (GFAP+) and endothelial (CD62E+) derived MPs, AV+ and tissue factor-bearing (TF+) MPs were measured using flow cytometry. Baseline levels of GFAP+/TF-, TF+/GFAP-, and GFAP+/TF+ MPs were significantly higher in GBM patients than in healthy controls, and significantly increased at each time point after surgery; at 7 months, a further significant increase over the level found a week after surgery was only seen in the subtotally resected patients. The number AV+/CD62E- MPs increased in GBM patients and correlated with MP activity. TF+/GFAP- MPs numbers were significantly higher in 11 GBM patients who developed VTE than in those who did not (p 0.04). TF+/GFAP- MPs levels above the 90th percentile (calculated in GBM patients without VTE) were associated with a higher risk of VTE (RR 4.17, 95% CI 1.57-11.03). In conclusion, the numbers of glial-derived and/or TF-bearing MPs were high in GBM patients both before and even more after the neoplasm was treated, especially in patients with subtotal resection likely according to disease progression. A contribution of TF+/GFAP- MPs to the risk of VTE is suggested.
Insights
Circulating microparticles (MPs), particularly glial-derived and tissue factor-bearing MPs, are elevated in glioblastoma multiforme (GBM) patients and may predict venous thromboembolism (VTE) risk after treatment.
Area of Science:
- Neuro-oncology
- Hematology
- Oncology
Background:
- Glioblastoma multiforme (GBM) patients frequently experience venous thromboembolism (VTE).
- Circulating microparticles (MPs) are implicated in cancer-associated VTE.
- Understanding MP profiles in GBM may reveal VTE risk factors.
Purpose of the Study:
- To investigate the association between circulating microparticle levels and VTE in glioblastoma patients.
- To evaluate changes in MP numbers and procoagulant activity post-surgery and treatment.
- To identify specific MP subsets that predict VTE risk in GBM.
Main Methods:
- Prospective evaluation of 61 GBM patients undergoing surgery and radio-chemotherapy.
- Measurement of microparticle numbers (glial-derived, endothelial, annexin V+, tissue factor-bearing) via flow cytometry.
- Correlation analysis of MP levels with VTE development and clinical outcomes.
Main Results:
- Baseline MP levels (GFAP+/TF-, TF+/GFAP-, GFAP+/TF+) were higher in GBM patients than controls.
- MP levels increased post-surgery, with sustained elevation in subtotally resected cases.
- Elevated TF+/GFAP- MPs were significantly associated with VTE development (p=0.04) and increased VTE risk (RR 4.17).
Conclusions:
- Glial-derived and tissue factor-bearing MPs are elevated in GBM patients, persisting and increasing post-treatment.
- Subtotal resection correlates with higher MP levels, potentially indicating disease progression.
- Tissue factor-bearing/glial-derived MPs (TF+/GFAP-) are a potential biomarker for predicting VTE risk in glioblastoma.
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