Immune reconstitution inflammatory syndrome in natalizumab-associated PML
- PMID: 21832229
- PMCID: PMC3174071
- DOI: 10.1212/WNL.0b013e31822e55e7
Immune reconstitution inflammatory syndrome in natalizumab-associated PML
Abstract
Objective: To study the outcome of patients with multiple sclerosis (MS) and with natalizumab-associated progressive multifocal leukoencephalopathy (PML) and immune reconstitution inflammatory syndrome (IRIS).
Methods: MedWatch reports from Biogen-Idec (manufacturer of natalizumab, Tysabri(®)) were reviewed which comprised all 42 cases of natalizumab-related PML cases since its reintroduction until March 2010.
Results: All except 2 patients with natalizumab-related PML were managed by discontinuation of natalizumab and plasmapheresis/immunoadsorption (PLEX/IA). Seventeen patients had contrast enhancement of PML lesions on neuroimaging at the time of diagnosis before withdrawal/removal of natalizumab (early-PML-IRIS) and 23 patients developed contrast enhancement only after withdrawal/removal of natalizumab (late-PML-IRIS). All patients developed IRIS. IRIS was defined as worsening of neurologic deficits during the immune reconstitution following discontinuation of natalizumab, corroborated by inflammatory changes on neuroimaging. Following PLEX/IA, JC viral load in CSF increased by >10 fold in those with early-PML-IRIS but <2 fold in late-PML-IRIS. IRIS developed earlier and was more severe in early-PML-IRIS (p < 0.05). At the last follow-up, all patients had worse EDSS scores but this was higher in patients with early-PML-IRIS compared to those with late-PML-IRIS (p > 0.05). Mortality was comparable between the 2 groups, 29.4 ± 11% vs 21.7 ± 8.8%. Corticosteroid therapy during IRIS was associated with better Expanded Disability Status Scale outcome, p < 0.05.
Conclusion: Early immunologic rebound in natalizumab-associated PML has worse survival and neurologic outcome. PLEX/IA may accelerate IRIS and its impact on the final outcome is unclear. Corticosteroid therapy provides a modest benefit and needs to be systemically studied in a controlled manner in the management of natalizumab-associated PML-IRIS.
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Comment in
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Too much of a good thing? IRIS with natalizumab-associated PML.Neurology. 2011 Sep 13;77(11):1033-4. doi: 10.1212/WNL.0b013e31822e14b7. Epub 2011 Aug 10. Neurology. 2011. PMID: 21832217 No abstract available.
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Immune reconstitution inflammatory syndrome in natalizumab-associated PML.Neurology. 2012 Jan 3;78(1):73; author response 73. doi: 10.1212/01.wnl.0000410335.08123.dc. Neurology. 2012. PMID: 22201114 No abstract available.
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Immune reconstitution inflammatory syndrome in natalizumab-associated PML.Neurology. 2012 Jan 31;78(5):371; author reply 371. doi: 10.1212/01.wnl.0000411451.56205.c3. Neurology. 2012. PMID: 22291067 No abstract available.
References
-
- Koralnik IJ. New insights into progressive multifocal leukoencephalopathy. Curr Opin Neurol 2004; 17: 365– 370 - PubMed
-
- Stüve O, Marra CM, Jerome KR, et al. Immune surveillance in multiple sclerosis patients treated with natalizumab. Ann Neurol 2006; 59: 743– 747 - PubMed
-
- Carson KR, Focosi D, Major EO, et al. Monoclonal antibody-associated progressive multifocal leukoencephalopathy in patients treated with rituximab, natalizumab, and efalizumab: a review from the Research on Adverse Drug Events and Reports (RADAR) Project. Lancet Oncol 2009; 10: 816– 824 - PubMed
-
- Bellizi A, Barucca V, Fioriti D, et al. Early years of biological agents therapy in Crohn's disease and risk of the human polyomavirus JC reactivation. J Cell Physiol Epub 2010 Apr 16 - PubMed
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