Author/Authors :
Kitazono، نويسنده , , Takako and Okazaki، نويسنده , , Takahiro and Araya، نويسنده , , Natsumi and Yamano، نويسنده , , Yoshihisa and Yamada، نويسنده , , Yasuaki and Nakamura، نويسنده , , Tatsufumi and Tanaka، نويسنده , , Yuetsu and Inoue، نويسنده , , Makoto and Ozaki، نويسنده , , Shoichi، نويسنده ,
Abstract :
Strong CTL response can be observed and associated with the control of proviral load in human T-lymphotropic virus type 1 (HTLV-1) infection. However, there are few details with regard to how HTLV-1 specific CTLs work against HTLV-1 infected cells and adult T-cell leukemia cells (ATLs). In this study, using Tax-specific CTL lines with high- and low-functional avidity developed from HLA-A2-transgenic mice, we showed that higher avidity CTLs specific for Tax expressing larger numbers of TCRs and better binding strength to the antigen-HLA-A2 complex are much more efficient at eliminating HTLV-1 infected cells and, in particular, ATL tumor cells with the ability of recognizing a latent level of Tax product detected only with a real-time PCR. These findings suggest that such higher avidity CTLs specific for Tax in HTLV-1 could be responsible for preventing the development of HTLV-1 infection by detecting trace amount of antigens.
Keywords :
ATL , avidity , Cytotoxic T-cell (CTL) , HTLV-1 , HLA-A2 transgenic mice