4.4 Article

Presence of JC virus-specific CTL in the cerebrospinal fluid of PML patients: rationale for immune-based therapeutic strategies

期刊

AIDS
卷 19, 期 18, 页码 2069-2076

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/01.aids.0000194804.97164.86

关键词

JC virus; progressive multifocal leukoencephalopathy; immunotherapy; cerebrospinal fluid; cytotoxic T lymphocytes; HIV; AIDS

资金

  1. NIAID NIH HHS [P30-AI28691] Funding Source: Medline
  2. NINDS NIH HHS [NS 047029, R01 NS/AI 041198] Funding Source: Medline

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Objectives: There is urgent need of a treatment for progressive multifocal leukoence-phalopathy (PML), caused by the polyornavirus JC (JCV). To evaluate the rationale for immunotherapy of PML, we explored whether JCV-specific cytotoxic T lymphocytes (CTL) can penetrate the central nervous system (CNS). In addition, we studied the breadth of their T-cell receptor (TCR) repertoire, and sought to establish a reliable method to expand these cells in vitro. Design and methods: We enrolled 18 patients in this study, including 16 with proven or possible PML (15 HIV-positive and one HIV-negative), and two HIV-positive patients with other neurological diseases. Detection of JCV-specific CTL in the blood and the cerebrospinal fluid was performed by Cr release and tetramer staining assays in 15 patients. Results: Of 11 PML patients with analyzable cerebrospinal fluid (CSF), two had no detectable JCV-specific CTL in the blood and CSF and died 3.7 and 7.2 months later. The nine remaining patients had an inactive course of PML and detectable JCV-specific CTL in the blood. In addition, four of them (44%) also had detectable JCV-specific CTL in the CSF. Both HIV-positive patients with OND had detectable JCV-specific CTL in the blood and one in the CSF. Using tetramer technology, we obtained highly enriched JCV-specific CTL lines that were able to kill target cells presenting JCV peptides. The breadth of the TCR repertoire was CTL epitope dependent. Conclusions: These results indicate that JCV-specific CTL are present in the CNS of PML patients and pave the way for an immune-based therapeutic approach. (c) 2005 Lippincott Williams & Wilkins.

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