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Toxoplasmic encephalitis during mycophenolate mofetil immunotherapy of neuromuscular disease
Danilo R Bernardo1, Nizar Chahin1
1Department of Neurology, University of North Carolina School of Medicine, Chapel Hill.
Objective:
To show that immunotherapy with medications such mycophenolate mofetil (MMF) can cause serious complications in patients with neuromuscular disorders.
Methods:
Two patients with neuromuscular disorders on immunotherapy with long-term MMF who developed toxoplasmic encephalitis (TE) were included in this case series.
Results:
One patient with myasthenia gravis and one patient with inflammatory myopathy on immunotherapy with long-term MMF developed severe TE. Diagnosis was based on clinical presentation, MRI brain imaging characteristics, and CSF PCR positivity for Toxoplasma gondii. Both patients were treated with pyrimethamine, sulfadiazine, and leucovorin for 2 months without clinical improvement, and both died.
Conclusions:
Immunotherapy with medications such as MMF can cause devastating TE in non-HIV patients with neuromuscular disorders. Early consideration and recognition of this complication is important to possibly prevent unfavorable outcomes. The utility of screening and prophylaxis against toxoplasmosis in individuals with neuroimmunologic disorders and other autoimmune disorders who receive immunosuppressive therapy requires future study.
Insights
Immunotherapy with mycophenolate mofetil (MMF) can lead to severe toxoplasmic encephalitis (TE) in patients with neuromuscular disorders. This serious complication, even in non-HIV individuals, necessitates early recognition and further study for prevention.
Area of Science:
- Neurology
- Immunology
- Infectious Diseases
Background:
- Immunosuppressive therapies, including mycophenolate mofetil (MMF), are used in managing various autoimmune and neuromuscular disorders.
- Opportunistic infections like toxoplasmic encephalitis (TE) are known risks in immunosuppressed populations.
Purpose of the Study:
- To highlight the potential for severe complications, specifically TE, in patients with neuromuscular disorders undergoing long-term immunotherapy with MMF.
- To underscore the importance of recognizing TE as a potential adverse effect of MMF in this patient group.
Main Methods:
- A case series approach was employed, focusing on two patients with neuromuscular disorders receiving long-term MMF therapy.
- Diagnosis of TE was confirmed through clinical presentation, characteristic MRI findings, and positive cerebrospinal fluid (CSF) PCR for *Toxoplasma gondii*.
Main Results:
- Two patients, one with myasthenia gravis and another with inflammatory myopathy, developed severe TE while on MMF.
- Despite standard treatment with pyrimethamine, sulfadiazine, and leucovorin for two months, both patients experienced no clinical improvement and ultimately died.
Conclusions:
- Long-term immunotherapy with MMF can precipitate devastating toxoplasmic encephalitis in non-HIV patients with neuromuscular disorders.
- Early recognition and consideration of TE are crucial for potentially improving outcomes in patients on MMF.
- Further research is needed to evaluate the efficacy of screening and prophylaxis for toxoplasmosis in individuals with neuroimmunologic and autoimmune disorders receiving immunosuppressive therapy.
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