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   DIR Return to: TYSABRI (natalizumab)
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       #Post#: 1846--------------------------------------------------
       (Abst.) Pathologic findings of chronic PML-IRIS in patient
       w/prolonged PML survival after Tysabri
   DIR By: agate
       Date: October 11, 2017, 11:59 am
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       Those who develop PML-IRIS in connection with taking Tysabri are
       usually stabilized in about 6 months but these researchers
       suggest that a patient who developed IRIS 3.5 years after
       developing Tysabri-related PML (and died) indicate that
       "prolonged low-grade inflammation may persist in some patients."
       From PubMed, October 11, 2017:
       --- Quote ---
       > J Investig Med High Impact Case Rep. 2017 Sep
       27;5(3):2324709617734248.
       >
       > Pathologic Findings of Chronic PML-IRIS in a Patient with
       Prolonged PML Survival Following Natalizumab Treatment
       >
       > Himedan M1, Camelo-Piragua S1, Mills EA1, Gupta A1, Aburashed
       R2, Mao-Draayer Y1.
       >
       > Author information
       >
       > 1
       > University of Michigan, Ann Arbor, MI, USA.
       > 2
       > Michigan State University, East Lansing, MI, USA.
       >
       > Immune reconstitution inflammatory syndrome (IRIS) is a common
       complication during treatment for natalizumab-associated
       progressive multifocal leukoencephalopathy (PML). Although
       severe IRIS can result in acute worsening of disability and is
       associated with poor prognosis, effective immune reconstitution
       may account for the high survival rate of this cohort of PML
       patients.
       >
       > We present pathological evidence of chronic IRIS 3.5 years
       after diagnosis with natalizumab-associated PML. Our case showed
       that the IRIS initially developed after plasma exchange therapy
       and resolved clinically and radiologically following a
       combination treatment with corticosteroids, maraviroc, and
       cidofovir.
       >
       > Autopsy 3.5 years later revealed evidence of grey-white matter
       junction demyelinating lesions characteristic of PML and
       perivascular leukocyte infiltrates predominated by CD8+
       T-lymphocytes, and polymerase chain reaction analysis
       demonstrated the presence of JC viral DNA in this tissue,
       indicative of persistent PML-IRIS. While clinical symptoms of
       PML-IRIS typically stabilize within 6 months, our case report
       suggests that prolonged low-grade inflammation may persist in
       some patients. Better assays are needed to determine the
       prevalence of prolonged low-grade IRIS among PML survivors.
       --- End Quote ---
       The abstract can be seen here
  HTML https://www.ncbi.nlm.nih.gov/pubmed/28989935.
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