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Updated: May 26, 2026

Modeling Chemotherapy Resistant Leukemia In Vitro
Published on: February 9, 2016
Cerebrospinal fluid IL-6, TNF-α and MCP-1 in children with acute lymphoblastic leukaemia during chemotherapy
P T Protas1, A Holownia, K Muszynska-Roslan
1Department of Clinical Pharmacology, Medical University of Bialystok, Poland. piotrp15@wp.pl
Insights
Chemotherapy for acute lymphoblastic leukaemia (ALL) in children may cause subclinical inflammation. Cerebrospinal fluid (CSF) cytokine levels, including interleukin-6 (IL-6) and tumour necrosis factor-α (TNF-α), increase during treatment, suggesting potential neurotoxicity.
Area of Science:
- Neuroscience
- Immunology
- Pediatric Oncology
Background:
- Acute lymphoblastic leukaemia (ALL) is a common childhood cancer.
- Chemotherapy is the standard treatment for ALL.
- Potential neurotoxic effects of chemotherapy are a concern in pediatric patients.
Purpose of the Study:
- To investigate changes in cerebrospinal fluid (CSF) cytokine levels during chemotherapy for ALL in children.
- To assess the relationship between CSF cytokine profiles and potential subclinical inflammation or neurotoxicity.
Main Methods:
- Analysis of CSF samples from 12 pediatric ALL patients.
- Measurement of cytokine levels including interleukin-6 (IL-6), monocyte chemotactic protein-1 (MCP-1), and tumour necrosis factor-α (TNF-α) at diagnosis, after induction, during consolidation, and post-therapy.
- Comparison of cytokine levels across different treatment phases.
Main Results:
- Significant increases in IL-6 and MCP-1 were observed after induction treatment.
- Elevated levels of IL-6, TNF-α, and MCP-1 were found during the consolidation phase compared to diagnosis.
- No significant differences in CSF cytokine levels were noted after completion of therapy.
Conclusions:
- Standard ALL chemotherapy may induce subclinical inflammation in the central nervous system.
- Elevated CSF cytokines suggest a potential for chemotherapy-induced neurotoxicity in pediatric ALL patients.
- Further research is needed to elucidate the long-term neurological consequences.
Abstract:
The aim of the study was to investigate the levels of cerebrospinal fluid (CSF) cytokines during chemotherapy of acute lymphoblastic leukaemia (ALL). Examination of 12 ALL child (6 boys and 6 girls) patients evidenced significant increases in interleukin-6 (IL-6) and monocyte chemotactic protein-1 (MCP-1) after induction treatment and significant increases in IL-6, tumour necrosis factor-α (TNF-α) and MCP-1 levels during the consolidation phase, as compared to their values at the time of diagnosis. There were no significant differences in CSF IL-6, TNF-α and MCP-1 concentrations after therapy. Our data suggest that standard ALL treatment may cause a subclinical inflammation and neurotoxicity.
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