Neuropsychiatric toxicity associated with cytokine therapies
D M Lerner1, A Stoudemire, D L Rosenstein
1Experimental Therapeutics Branch, National Institute of Mental Health, Bethesda, MD 20892-1274, USA.
Abstract:
The cytokines interleukin-2 and interferon-alpha are potent biological agents used to treat malignancy, infectious diseases, and neurodegenerative disorders. While these medications show substantial therapeutic promise, the neuropsychiatric toxicity associated with these agents is often treatment-limiting. The pathophysiology of this toxicity is not well delineated, and adverse effects to the central nervous system are often misdiagnosed by clinicians. This report reviews the preclinical and clinical literature describing the morbidity associated with these agents and suggests appropriate clinical management strategies and future directions for research.
Insights
Interleukin-2 and interferon-alpha therapies, while effective for various diseases, can cause limiting neuropsychiatric side effects. Understanding and managing these central nervous system toxicities is crucial for patient care.
Area of Science:
- Immunology
- Neuroscience
- Oncology
Background:
- Interleukin-2 (IL-2) and interferon-alpha (IFN-α) are critical biologic agents for treating cancers, infections, and neurodegenerative conditions.
- A significant challenge limiting the use of IL-2 and IFN-α is their associated neuropsychiatric toxicity.
- The mechanisms underlying these central nervous system (CNS) adverse effects are not fully understood, leading to frequent misdiagnosis.
Purpose of the Study:
- To review the existing preclinical and clinical literature on the neuropsychiatric toxicities of IL-2 and IFN-α.
- To delineate the morbidity associated with these biologic agents.
- To propose clinical management strategies and identify future research directions.
Main Methods:
- Comprehensive literature search of preclinical and clinical studies.
- Analysis of reported cases and experimental data on IL-2 and IFN-α induced neurotoxicity.
- Synthesis of findings to inform clinical practice and research.
Main Results:
- Documented evidence of significant neuropsychiatric adverse events linked to IL-2 and IFN-α therapy.
- Identification of common CNS manifestations and potential pathophysiological pathways.
- Highlighting diagnostic challenges and the need for specialized clinical awareness.
Conclusions:
- Neuropsychiatric toxicity is a critical dose-limiting factor for IL-2 and IFN-α therapies.
- Improved understanding of pathophysiology is needed for accurate diagnosis and effective management.
- Further research is essential to develop targeted interventions and optimize patient outcomes.
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