Inhibition of human T-cell leukemia virus type 1 replication by antisense env oligodeoxynucleotide

被引:6
作者
Maeda, N
Kawamura, T
Hoshino, H
Yamada, N
Blackard, J
Kushida, S
Miyano-Kurosaki, N
Yamamoto, N
Makino, K
Yokota, T
Uchida, K
Miwa, M [1 ]
机构
[1] Univ Tsukuba, Inst Basic Med Sci, Dept Biochem & Mol Oncol, Tsukuba, Ibaraki 305, Japan
[2] Univ Tsukuba, Ctr Tsukuba Adv Res Alliance, Tsukuba, Ibaraki 305, Japan
[3] Gunma Univ, Sch Med, Dept Hyg & Virol, Maebashi, Gumma 371, Japan
[4] Tokyo Med & Dent Univ, Sch Med, Dept Mol Virol & Microbiol, Bunkyo Ku, Tokyo 113, Japan
[5] Kyoto Inst Technol, Fac Text Sci, Dept Polymer Sci & Engn, Sakyo Ku, Kyoto 606, Japan
[6] Rat Drug Design Labs, Fukushima, Japan
关键词
D O I
10.1006/bbrc.1997.8039
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human T-cell leukemia virus type 1 (HTLV-1) infection is associated with adult T-cell leukemia and HTLV-associated myelopathy/tropical spastic paraparesis. inhibition of HTLV-1 transmission is important to prevent the above HTLV-1-associated diseases. We used the antisense oligodeoxynucleotides (oligos) complementary to the first splice junction, rex responsive site, gag, enu, tax, rex, and p21 and evaluated the effects on the syncytium formation between HTLV-1 producing human T-cell line, C91/PL cells, and HTLV-1-uninfected human glioma cell Line, U251-MG cells. The syncytium formation was significantly inhibited the virion production assayed by antisense oligos to env, tax, gag, p21, and rex, with antisense oligo to env being the most inhibitory. Antisense oligos to env and tax also inhibited reverse transcriptase activity. Antisense oligo to env may have a potential as a preventive measure of HTLV-1 replication and transmission in vivo. (C) 1998 Academic Press.
引用
收藏
页码:109 / 112
页数:4
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