Direct visualization of antigen-specific T cells: HTLV-1 Tax11–19- specific CD8+ T cells are activated in peripheral blood and accumulate in cerebrospinal fluid from HAM/TSP patients

  1. Tim F. Greten*,,
  2. Jill E. Slansky*,
  3. Ryuji Kubota,
  4. Samantha S. Soldan,
  5. Elizabeth M. Jaffee*,
  6. Thomas P. Leist,
  7. Drew M. Pardoll*,
  8. Steven Jacobson, and
  9. Jonathan P. Schneck*
  1. *Department of Oncology and Pathology, Johns Hopkins University School of Medicine, 720 Rutland Avenue, Ross 364, Baltimore, MD 21205; and Viral Neuroimmunology Section, National Institute of Neurologic Disorders and Stroke, Building 10, Room 5B-16, 9000 Rockville Pike, Bethesda, MD 20892
  1. Communicated by John W. Kappler, National Jewish Medical and Research Center, Denver, CO (received for review March 3, 1998)

Abstract

Human T lymphotropic virus type 1 (HTLV-1) -associated myelopathy/tropic spastic paraparesis is a demyelinating inflammatory neurologic disease associated with HTLV-1 infection. HTLV-1 Tax11–19-specific cytotoxic T cells have been isolated from HLA-A2-positive patients. We have used a peptide-loaded soluble HLA-A2–Ig complex to directly visualize HTLV-1 Tax11–19-specific T cells from peripheral blood and cerebrospinal fluid without in vitro stimulation. Five of six HTLV-1-associated myelopathy/tropic spastic paraparesis patients carried a significant number (up to 13.87%) of CD8+ lymphocytes specific for the HTLV-1 Tax11–19 peptide in their peripheral blood, which were not found in healthy controls. Simultaneous comparison of peripheral blood and cerebrospinal fluid from one patient revealed 2.5-fold more Tax11–19-specific T cells in the cerebrospinal fluid (23.7% vs. 9.4% in peripheral blood lymphocyte). Tax11–19-specific T cells were seen consistently over a 9-yr time course in one patient as far as 19 yrs after the onset of clinical symptoms. Further analysis of HTLV-1 Tax11–19-specific CD8+ T lymphocytes in HAM/TSP patients showed different expression patterns of activation markers, intracellular TNF-α and γ-interferon depending on the severity of the disease. Thus, visualization of antigen-specific T cells demonstrates that HTLV-1 Tax11–19-specific CD8+ T cells are activated, persist during the chronic phase of the disease, and accumulate in cerebrospinal fluid, showing their pivotal role in the pathogenesis of this neurologic disease.

Footnotes

  • To whom reprint requests should be addressed. e-mail: tgreten{at}welchlink.welch.jhu.edu.

  • ABBREVIATIONS:
    HTLV-1,
    human T lymphotropic virus 1;
    HAM/TSP,
    HTLV-1-associated myelopathy/tropic spastic paraparesis;
    PBL,
    peripheral blood lymphocyte;
    CTL,
    cytotoxic T lymphocyte;
    CSF cerebrospinal fluid,
    IL, interleukin;
    IFN-γ,
    γ-interferon;
    TNF-α,
    tumor necrosis factor α;
    FITC,
    fluorescein isothiocyanate;
    PE,
    phycoerythrin;
    LDA,
    limiting dilution analysis;
    MHC,
    major histocompatibility complex
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