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Circulating T-regulatory cells in neuroblastoma: a pilot prospective study
Tvsvgk Tilak1, Surender Sherawat, Sandeep Agarwala
1Department of Medical Oncology.
Pediatric Hematology and Oncology
|April 2, 2014
Summary
Neuroblastoma patients have higher regulatory T cell (Treg) levels than healthy controls. Treg frequency decreases with neoadjuvant chemotherapy but may increase at relapse, indicating their role in neuroblastoma progression.
Area of Science:
- Immunology
- Pediatric Oncology
Background:
- Regulatory T cells (Tregs) play a crucial role in immune regulation.
- Altered Treg levels are implicated in various cancers, including neuroblastoma.
Purpose of the Study:
- To determine baseline regulatory T cell (Treg) frequencies in neuroblastoma patients.
- To correlate Treg levels with patient characteristics, therapeutic response, and disease progression.
- To assess changes in Treg frequency during neoadjuvant chemotherapy and at relapse.
Main Methods:
- Flow-cytometric analysis of Treg cells (CD4+CD25+FoxP3+) was performed.
- Samples were collected from 14 de novo neuroblastoma patients at diagnosis, post-chemotherapy, and at relapse.
- Six healthy controls were included for comparison.
Main Results:
- Neuroblastoma patients exhibited significantly higher baseline Treg frequencies compared to healthy controls (9.84% vs 3.16%, P < .001).
- Higher Treg frequency was observed in patients with tumors larger than 10 cm (P = .004).
- Neoadjuvant chemotherapy led to a significant reduction in Treg frequency (3.07% vs 9.72%, P = .007).
Conclusions:
- Elevated baseline Treg levels are characteristic of neuroblastoma patients.
- Treg frequency is associated with tumor burden and is modulated by chemotherapy.
- Tregs may represent a therapeutic target or a marker for monitoring neuroblastoma response and progression.

