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Updated: Aug 17, 2025

Nerve Ultrasound Protocol to Detect Dysimmune Neuropathies
Published on: October 7, 2021
Characteristic cerebrospinal fluid findings in immune checkpoint inhibitor-related peripheral neuropathy: A case
Sho Wako1, Ryotaro Ikeguchi1, Kunio Toda1
1Department of Neurology, Tokyo Women's Medical University, Tokyo, Japan.
Insights
Immune checkpoint inhibitors (ICIs) can cause peripheral neuropathy. Cerebrospinal fluid analysis revealed elevated cytokines and soluble interleukin-2 receptor, suggesting T cell autoimmunity and potential biomarkers for diagnosis.
Area of Science:
- Neuroimmunology
- Oncology
- Biomarker Discovery
Background:
- Immune checkpoint inhibitors (ICIs) are crucial for treating unresectable tumors.
- Immune-related adverse events (irAEs), including neurological toxicities, are known side effects of ICIs.
- Peripheral neuropathy is a significant neurological irAE.
Observation:
- A case of ICI-related peripheral neuropathy (irPN) presented with specific cerebrospinal fluid (CSF) abnormalities.
- CSF analysis revealed not only pleocytosis and elevated protein levels but also increased concentrations of soluble interleukin-2 receptor (sIL-2R), IL-6, and IL-10.
- These CSF findings suggest an underlying T cell-mediated autoimmune process.
Findings:
- The study identified elevated CSF sIL-2R, IL-6, and IL-10 levels in a patient with irPN.
- These elevated cytokines and sIL-2R indicate a role for activated T cells in the pathogenesis of irPN.
- The findings highlight a potential link between specific CSF cytokine profiles and ICI-induced neuropathy.
Implications:
- CSF sIL-2R, IL-6, and IL-10 may serve as novel biomarkers for diagnosing irPN.
- Identifying these biomarkers could lead to earlier diagnosis and more targeted management of ICI-related neurological toxicities.
- This research contributes to understanding the mechanisms of neurotoxicity associated with immunotherapy.
Abstract:
Although immune checkpoint inhibitors (ICIs) are widely used to treat unresectable malignant tumors, they can cause undesirable side effects called immune-related adverse events, including neurological toxicities. Here, we describe a case of ICI-related peripheral neuropathy (irPN) with characteristic cerebrospinal fluid (CSF) findings. In addition to pleocytosis and increased protein levels, the present case showed increased levels of CSF soluble interleukin-2 receptor (sIL-2R), IL-6, and IL-10, suggesting activated T cell-related autoimmunity. We believe that CSF cytokines and sIL-2R could be novel biomarkers of irPN.
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