The Journal of Immunology · 1999 · 133 citations · 33 references
Life SciencesImmunologyPathologyCellular ImmunologyImmunopathologyNeuroimmunologyAntigen RecognitionCell-mediated ImmunityHla TypingHuman Leukocyte Antigen SystemT Cell ActivationT Cell BiologyCd8 Positive T CellsClonal ExpansionClonal Expansion Of LymphocytesHla Class I MoleculesImmune InfiltratesMhc Class I MoleculesT Cell Clonal ExpansionT-cell Immune Responses
Human T cell lymphotropic virus-I (HTLV-I)-associated myelopathy is a slowly progressive neurologic disease characterized by inflammatory infiltrates in the central nervous system accompanied by clonal expansion of HTLV-I-reactive CD8+ T-cells. In patients carrying the HLA-A2 allele, the immune response is primarily directed to the Tax11-19 peptide. The frequency, activation state, and TCR usage of HLA-A2/Tax11-19 binding T cells in patients with HTLV-I-associated myelopathy was determined using MHC class I tetramers loaded with the Tax11-19 peptide. Circulating Tax11-19-reactive T cells were found at very high frequencies, approaching 1:10 circulating CD8+ T cells. T cells binding HLA-A2/Tax11-19 consisted of heterogeneous populations expressing different chemokine receptors and the IL-2R beta-chain but not the IL-2R alpha-chain. Additionally, Tax11-19-reactive CD8+ T cells used one predominant TCR Vbeta-chain for the recognition of the HLA-A2/Tax11-19 complex. These data provide direct evidence for high frequencies of circulating Tax11-19-reactive CD8+ T cells in patients with HTLV-I-associated myelopathy.
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