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Determining Immune System Suppression versus CNS Protection for Pharmacological Interventions in Autoimmune Demyelination
Published on: September 12, 2016
Disease-modifying therapies and infectious risks in multiple sclerosis
Alexander Winkelmann1, Micha Loebermann2, Emil C Reisinger2
1Department of Neurology, University of Rostock, Gehlsheimer Strasse 20, 18147 Rostock, Germany.
Abstract:
Immunomodulatory and immunosuppressive treatments for multiple sclerosis (MS) are associated with an increased risk of infection, which makes treatment of this condition challenging in daily clinical practice. Use of the expanding range of available drugs to treat MS requires extensive knowledge of treatment-associated infections, risk-minimizing strategies and approaches to monitoring and treatment of such adverse events. An interdisciplinary approach to evaluate the infectious events associated with available MS treatments has become increasingly relevant. In addition, individual stratification of treatment-related infectious risks is necessary when choosing therapies for patients with MS, as well as during and after therapy. Determination of the individual risk of infection following serial administration of different immunotherapies is also crucial. Here, we review the modes of action of the available MS drugs, and relate this information to the current knowledge of drug-specific infectious risks and risk-minimizing strategies.
Insights
Multiple sclerosis (MS) treatments increase infection risk. This review details drug actions, infection risks, and strategies to manage infections in MS patients.
Area of Science:
- Neuroimmunology
- Infectious Disease Management in Autoimmune Disorders
Background:
- Immunomodulatory and immunosuppressive therapies for multiple sclerosis (MS) are linked to a higher incidence of infections.
- Managing these treatment-associated infections presents a significant challenge in routine clinical practice for MS patients.
- The growing array of available MS drugs necessitates comprehensive understanding of their infection risks and management protocols.
Purpose of the Study:
- To review the mechanisms of action for current multiple sclerosis drugs.
- To correlate drug mechanisms with known infection risks associated with each therapy.
- To outline strategies for minimizing and managing treatment-related infections in MS patients.
Main Methods:
- Literature review of immunomodulatory and immunosuppressive treatments for multiple sclerosis.
- Analysis of drug mechanisms of action in relation to infectious complications.
- Synthesis of current knowledge on drug-specific infection risks and risk-mitigation strategies.
Main Results:
- Different MS therapies possess distinct mechanisms that influence susceptibility to specific infections.
- Understanding these drug-specific risks is crucial for proactive management.
- Individualized risk stratification is essential for selecting and monitoring MS therapies.
Conclusions:
- An interdisciplinary approach is vital for evaluating and managing infectious events in patients undergoing MS treatment.
- Personalized assessment of infection risk is necessary before, during, and after immunotherapy for multiple sclerosis.
- Knowledge of drug actions and associated infectious risks informs safer and more effective MS treatment strategies.
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