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Fingolimod-related cryptococcal meningoencephalitis and immune reconstitution inflammatory syndrome in a patient with
Fernando X Cuascut1, Samir Alkabie1, George J Hutton1
1Maxine Mesinger Multiple Sclerosis Comprehensive Care Center, Department of Neurology, Baylor College of Medicine, Houston, Texas, United States.
Abstract:
Fingolimod is an oral medication for multiple sclerosis that sequesters certain subsets of lymphocytes in lymph nodes, reducing egress into blood and their subsequent CNS migration. The initial multi-site randomized Phase III controlled trials found rates of infection similar to those in control groups. However, post-marketing surveillance has revealed an association with several opportunistic infections, including cryptococcosis. We report a case of fingolimod-related cryptococcal meningoencephalitis and IRIS after drug discontinuation and suggest a surveillance and risk mitigation strategy.
Insights
Fingolimod, an oral multiple sclerosis drug, can lead to serious opportunistic infections like cryptococcosis. This case highlights the need for careful monitoring and risk management strategies, especially after discontinuing the medication.
Area of Science:
- Neuroimmunology
- Infectious Diseases
- Pharmacology
Background:
- Fingolimod is an oral disease-modifying therapy for multiple sclerosis (MS) that reduces lymphocyte trafficking to the central nervous system (CNS).
- Initial Phase III trials reported infection rates comparable to placebo groups.
- Post-marketing data have indicated an increased risk of opportunistic infections with fingolimod use.
Observation:
- A case of cryptococcal meningoencephalitis and immune reconstitution inflammatory syndrome (IRIS) is presented in a patient treated with fingolimod.
- The infection and IRIS occurred after the discontinuation of fingolimod therapy.
Findings:
- Fingolimod-associated cryptococcosis can manifest even after drug cessation.
- IRIS can complicate the course of opportunistic infections in patients previously treated with immunomodulatory drugs like fingolimod.
Implications:
- Enhanced surveillance for opportunistic infections, particularly cryptococcosis, is crucial in patients treated with fingolimod.
- Risk mitigation strategies should be developed to manage potential infections and IRIS following fingolimod discontinuation.
- This case underscores the importance of considering delayed adverse effects of immunosuppressive therapies in MS management.
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