AI Article Synopsis

  • Progressive Multifocal Leukoencephalopathy (PML) is a serious brain disease caused by the JC virus, primarily affecting individuals with weakened immune systems, such as those with AIDS or on strong immunosuppressive drugs like natalizumab for multiple sclerosis.
  • A new blood test called the IFN-γ release assay (IGRA) was developed to detect specific immune responses to the JC virus, showing high sensitivity (84%) in active PML patients and very low false positives (3% in healthy individuals).
  • The test's results indicate a potential for identifying patients at increased risk of PML, as its positivity rate rises with longer treatment durations on immunosuppressive therapies like natal

Article Abstract

Introduction: Progressive Multifocal Leukoencephalopathy (PML) is a rare and deadly demyelinating disease caused by JC virus (JCV) replication in the central nervous system. PML occurs exclusively in patients with severe underlying immune deficiencies, including AIDS and hematological malignancies. PML has also emerged as a significant threat to patients on potent new immunosuppressive biologics, including natalizumab in multiple sclerosis.

Methods: Here, we developed an IFN-γ release assay (IGRA) that mainly detects JCV-specific effector memory T cells and effectors T cells in the blood.

Results: This assay was frequently positive in patients with active PML (with a positive JCV PCR in CSF) of various underlying immunosuppression causes (84% sensitivity). Only 3% of healthy donors had a positive response (97% specificity). The frequency of positivity also increased in multiple sclerosis patients according to the time on natalizumab (up to 36% in patients treated for more than 48 months, who are considered at a higher risk of PML).

Discussion: The results show this assay's frequent or increased positivity in patients with PML or an increased risk of PML, respectively. The assay may help to stratify the risk of PML.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11289500PMC
http://dx.doi.org/10.3389/fimmu.2024.1416074DOI Listing

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