Abstract
Most immunosuppressed individuals who develop progressive multifocal leukoencephalopathy (PML) have a rapid fatal outcome, whereas some become long-term survivors. We explored the impact of the cellular immune response against JC virus (JCV) on the clinical outcome of 7 HIV + and 3 HIV - individuals with PML. Of the 4 HIV +/PML survivors, all had detectable cytotoxic T lymphocytes (CTL) specific for JCV T or VP 1 proteins compared to none of the 3 HIV +/PML progressors tested. Of the 3 HIV -/PML patients, 1 was recently diagnosed with PML and showed evidence of neurologic improvement without any treatment. This patient had CTL specific for the VP1 protein of JCV. The other 2 HIV -/PML survivors were stable 3-8 years after the diagnosis of PML. They did not have any detectable CTL against JCV. These findings suggest that JCV-specific immune response is associated with favorable outcome in HIV + individuals with PML. The lack of detectable JCV-specific CTL in 2 HIV -/PML survivors might indicate a burnt-out disease without sufficient antigenic stimulation to maintain the cellular immune response. The detection of JCV-specific CTL in an HIV - patient recently diagnosed with PML, who was showing evidence of neurological improvement without any treatment, indicates that this finding may be used as a favorable prognostic marker of disease evolution in the clinical management of patients with PML. As the quest for an effective treatment of PML continues, JCV-specific cellular immune response deserves further attention because it appears to play a crucial role in the prevention of disease progression.
Original language | English (US) |
---|---|
Pages (from-to) | 318-322 |
Number of pages | 5 |
Journal | Journal of neurovirology |
Volume | 7 |
Issue number | 4 |
DOIs | |
State | Published - 2001 |
Keywords
- Acquired immune deficiency syndrome (AIDS)
- Cytotoxic T lymphocytes
- Human immunodeficiency virus (HIV)
- Progressive multifocal leukoencephalopathy (PML)
ASJC Scopus subject areas
- Neurology
- Clinical Neurology
- Cellular and Molecular Neuroscience
- Virology