Kannagi M, Matsushita S, Shida H, Harada S
Department of Biodefence and Medical Virology, Kumamoto University School of Medicine, Japan.
Leukemia. 1994 Apr;8 Suppl 1:S54-9.
The cytotoxic T cell response of peripheral blood mononuclear cells (PBMC) to in vitro stimulation with human T cell leukemia virus type I (HTLV-I) was compared among HTLV-I-infected individuals with various clinical conditions. Induction of HTLV-I-specific cytotoxic T lymphocytes (CTL) was observed in 57% of asymptomatic HTLV-I carriers, 86% of patients with HTLV-I associated myelopathy/tropical spastic paraparesis (HAM/TSP) or other HTLV-I-related inflammatory diseases, and 18% of adult T cell leukemia (ATL) patients. HTLV-I p40tax, one of the major CTL target antigens, has an epitope strongly associated with HLA-A2. HTLV-I p40tax-specific CTL were frequently induced from HLA-A2-positive donors with HTLV-I-related inflammatory diseases regardless of neurological symptoms, but not from all the HLA-A2-positive HTLV-I-infected individuals tested. Leukemic cells of an ATL patient with HLA-A2, whose PBMC did not show an HTLV-I-specific CTL response, could be lyzed by p40tax-specific CTL derived from an HAM/TSP patient. This indicates that i) the presence of a certain HLA presenting CTL epitopes is not the sole determinant of the individual CTL response to HTLV-I, ii) HTLV-I-specific CTL act as potential effectors of anti-tumor surveillance in vivo. The role of HTLV-I-specific CTL, however, may be limited by another in vivo mechanism suppressing the expression of HTLV-I antigens. This suppression, presumably mediated by a plasma factor and commonly observed in HTLV-I-infected individuals, could be one reason for the persistence of HTLV-I-infection.
在患有各种临床病症的人类嗜T淋巴细胞病毒I型(HTLV-I)感染个体中,比较了外周血单个核细胞(PBMC)对HTLV-I体外刺激的细胞毒性T细胞反应。在57%的无症状HTLV-I携带者、86%的HTLV-I相关脊髓病/热带痉挛性截瘫(HAM/TSP)或其他HTLV-I相关炎症性疾病患者以及18%的成人T细胞白血病(ATL)患者中观察到了HTLV-I特异性细胞毒性T淋巴细胞(CTL)的诱导。HTLV-I p40tax是主要的CTL靶抗原之一,具有与HLA-A2强烈相关的表位。无论有无神经症状,HTLV-I p40tax特异性CTL经常从患有HTLV-I相关炎症性疾病的HLA-A2阳性供体中诱导产生,但并非来自所有检测的HLA-A2阳性HTLV-I感染个体。一名具有HLA-A2的ATL患者的白血病细胞,其PBMC未显示HTLV-I特异性CTL反应,可被来自HAM/TSP患者的p40tax特异性CTL裂解。这表明:i)存在某些呈递CTL表位的HLA不是个体对HTLV-I的CTL反应的唯一决定因素;ii)HTLV-I特异性CTL在体内作为抗肿瘤监视的潜在效应器。然而,HTLV-I特异性CTL的作用可能受到另一种抑制HTLV-I抗原表达的体内机制的限制。这种抑制可能由一种血浆因子介导,在HTLV-I感染个体中普遍观察到,可能是HTLV-I感染持续存在的一个原因。