Kubota Ryuji, Soldan Samantha S, Martin Roland, Jacobson Steven
Neuroimmunology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892, USA.
J Neurovirol. 2002 Feb;8(1):53-7. doi: 10.1080/135502802317247811.
Human T lymphotropic virus type I (HTLV-I)-associated myelopathy/tropical spastic paraparesis (HAM/TSP) is a chronic inflammatory disease of the spinal cord in which HTLV-I Tax-specific cytotoxic T lymphocytes (CTL) have been suggested to be immunopathogenic. However, it is unknown whether the HTLV-I-specific CTL in the central nervous system differ from those in the periphery. We investigated functional T-cell receptor diversity in HTLV-I Tax11-19-specific CTL clones derived from peripheral blood and cerebrospinal fluid (CSF) of a HAM/TSP patient using analogue peptides of the viral antigen. CTL responses to the analogue peptides varied between T-cell clones, however, CTL clones from CSF showed limited recognition of the peptides when compared to those from peripheral blood. This suggests that CTL with highly focused specificity for HTLV-I Tax accumulate in the CSF and may contribute to the pathogenesis of HAM/TSP. Furthermore, this study provides a rationale for analogue peptide-based immunotherapeutic strategies focusing on the immunopathogenic T-cells in HTLV-I-associated neurologic disease.
人类嗜T淋巴细胞病毒I型(HTLV-I)相关脊髓病/热带痉挛性截瘫(HAM/TSP)是一种脊髓慢性炎症性疾病,其中HTLV-I Tax特异性细胞毒性T淋巴细胞(CTL)被认为具有免疫致病性。然而,尚不清楚中枢神经系统中HTLV-I特异性CTL是否与外周的CTL不同。我们使用病毒抗原的模拟肽研究了从一名HAM/TSP患者的外周血和脑脊液(CSF)中获得的HTLV-I Tax11-19特异性CTL克隆的功能性T细胞受体多样性。T细胞克隆对模拟肽的CTL反应各不相同,然而,与外周血来源的CTL克隆相比,脑脊液来源的CTL克隆对这些肽的识别有限。这表明对HTLV-I Tax具有高度聚焦特异性的CTL在脑脊液中积聚,并可能导致HAM/TSP的发病机制。此外,本研究为基于模拟肽的免疫治疗策略提供了理论依据,该策略聚焦于HTLV-I相关神经疾病中的免疫致病性T细胞。