Flow cytometry evaluation of the T-cell receptor Vβ repertoire among human T-cell lymphotropic virus type-1 (HTLV-1) infected individuals:: Effect of interferon alpha therapy in HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP)

被引:2
作者
Saito, Mineki
Nose, Hirohisa
Usuku, Koichiro
Sabouri, Amir H.
Matsuzaki, Toshio
Izumo, Shuji
Arimura, Kimiyoshi
Osame, Mitsuhiro
机构
[1] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Neurol & Geriat, Kagoshima 8908520, Japan
[2] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Med Informat Sci, Kagoshima 8908520, Japan
[3] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Mol Pathol, Ctr Chron Viral Dis, Kagoshima 8908520, Japan
关键词
interferon-alpha; T cell receptor V beta repertoire; HTLV-1; HAM/TSP;
D O I
10.1016/j.jns.2006.02.004
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Human T-cell lymphotropic virus type-1 (HTLV-1)-associated myelopathy/tropical spastic paraparesis (HAM/TSP) is chronic inflammatory disease of the spinal cord characterized by perivascular lymphocytic cuffing and parenchymal lymphocytic infiltration. In this study using flow cytometry, we have investigated the T-cell receptor (TCR) V beta repertoire of peripheral blood T lymphocytes in 8 HAM/ TSP patients, 10 HTLV-1 infected healthy carriers, and 11 uninfected healthy controls to determine if there is a biased usage of TCR V beta. We found that TCR V beta 7.2 was under-utilized and V beta 12 was over-utilized in CD4(+) T cells of HTLV-1 infected individuals compared with healthy uninfected controls, whereas there were no such differences in CD8(+) T cells. Comparison of V beta repertoire changes before and after interferon-alpha (IFN-alpha) treatment for HAM/TSP revealed that one out of five patients showed dramatic decrease of specific V in CD8(+) T cells. Our results suggest that dominant V beta subpopulations in CD4(+) T cells evolved associated with chronic HTLV-1 infection, and IFN-alpha treatment for HAM/TSP does not induce a specific pattern of TCR V changes. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:37 / 43
页数:7
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