Maraviroc in PML-IRIS

Progressive multifocal leukoencephalpathy (PML) is a severe, often fatal, opportunistic infection of the CNS. First reported in 1958 as a white matter disorder in 3 patients with lymphoproliferative disorders, subsequent studies revealed a polyomavirus, named John Cunningham (JC) virus from the initials of the patient from whose brain it was initially isolated, as the causative agent. Despite previous reports, there is no evidence that PML is caused by either SV40 or BK virus. The pathogen is a ubiquitous DNA virus that infects only humans. Subclinical infection often takes place within the first decade of life. Both the mechanism of infection and clinical expression of primary infection remain undefined. Initially, predominantly associated with lymphoproliferative disorders, with the AIDS pandemic, PML became strikingly prevalent, observed in 4%–5% of all patients with HIV prior to the availability of highly active antiretroviral therapy (HAART). The era of monoclonal antibodies for immune-mediated conditions such as natalizumab (Tysabri) for MS and Crohn disease and efalizumab (Raptiva) for psoriasis heralded another context for PML. As of November 30, 2016, there have been 698 reported cases of PML under natalizumab. While HAART has a significant beneficial impact on the prognosis of PML in patients with HIV, it remains one of the 4 most common CNS opportunistic infections affecting patients with AIDS. The institution of screening patients with MS for seropositivity for JC virus has decreased the prevalence of PML in natalizumab-treated patients with MS. The termination of this therapy and using plasma exchange to remove the monoclonal antibody from the circulation when PML is diagnosed has a beneficial effect on prognosis. However, the introduction of HAART and the discontinuation of natalizumab led to the recognition of the immune reconstitution inflammatory syndrome (IRIS), an entity that is not unique to PML and has been observed also with mycobacterial diseases, leprosy, fungal infections, and herpes viruses. IRIS is the consequence of rapid entry of immune cells into the brain at the time of immune restoration. As many as 23% of patients with AIDS with PML who recently started HAART will develop PMLIRIS. IRIS has occurred in the majority of patients with natalizumab-associated PML following withdrawal of natalizumab and plasma exchange. The diagnosis of CNS-IRIS in patients with MS with natalizumab-associated PML can be challenging because the deterioration might be attributed to PML, MS, or some other opportunistic infection. Thus, diagnosis of PML in an immunecompromised patient is associated with a 2-edge challenge and risk: clearing the JC virus from the brain, which requires normalization of the immune state, and reconstitution of immune surveillance while minimizing infiltration of the brain with activated T cells that attempt to control an underlying CNS opportunistic infection. Treatment of CNS-IRIS is mainly empirical; as of today, there are no randomized controlled trials to support antiviral or immune-modulating therapy in this condition. The suggestion to treat CNS-IRIS with steroids remains at present a hypothesis. In 2009, a case report on the use of maraviroc, a CCR5 antagonist that has been approved for the treatment of HIV infection to inhibit CCR5dependent viral docking in AIDS suggested that this agent might be effective against CNS-IRIS. The observation was not confirmed in a large study. Maraviroc is also associated with blocking of CCR5-mediated inflammation and was reported to be beneficial in graft-vs-host disease in patients undergoing allogenic bone marrow transplantation. It also decreases the amount of CD8 cells in the CNS of patients. This led to an effort to extrapolate the use of maraviroc to PML under monoclonal antibodies therapy for MS. This was associated with reduced trafficking of CCR5-expressing cells into