The Chinese herb-derived Sparstolonin B suppresses HIV-1 transcription
被引:18
作者:
Deng, Xin
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机构:
Guangxi Univ Chinese Med, Ruikang Hosp, Dept Infect Dis, Nanning 530011, Peoples R ChinaGuangxi Univ Chinese Med, Ruikang Hosp, Dept Infect Dis, Nanning 530011, Peoples R China
Deng, Xin
[1
]
Zhang, Yaping
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Guangxi Univ Chinese Med, Ruikang Hosp, Dept Infect Dis, Nanning 530011, Peoples R ChinaGuangxi Univ Chinese Med, Ruikang Hosp, Dept Infect Dis, Nanning 530011, Peoples R China
Zhang, Yaping
[1
]
Jiang, Feng
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Guangxi Univ Chinese Med, Ruikang Hosp, Dept Infect Dis, Nanning 530011, Peoples R ChinaGuangxi Univ Chinese Med, Ruikang Hosp, Dept Infect Dis, Nanning 530011, Peoples R China
Jiang, Feng
[1
]
Chen, Ran
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Guangxi Univ Chinese Med, Ruikang Hosp, Dept Infect Dis, Nanning 530011, Peoples R ChinaGuangxi Univ Chinese Med, Ruikang Hosp, Dept Infect Dis, Nanning 530011, Peoples R China
Chen, Ran
[1
]
Peng, Peichun
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Guangxi Univ Chinese Med, Ruikang Hosp, Dept Infect Dis, Nanning 530011, Peoples R ChinaGuangxi Univ Chinese Med, Ruikang Hosp, Dept Infect Dis, Nanning 530011, Peoples R China
Peng, Peichun
[1
]
Wen, Bin
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Guangxi Univ Chinese Med, Ruikang Hosp, Dept Infect Dis, Nanning 530011, Peoples R ChinaGuangxi Univ Chinese Med, Ruikang Hosp, Dept Infect Dis, Nanning 530011, Peoples R China
Wen, Bin
[1
]
Liang, Jian
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Guangxi Univ Chinese Med, Ruikang Hosp, Dept Infect Dis, Nanning 530011, Peoples R ChinaGuangxi Univ Chinese Med, Ruikang Hosp, Dept Infect Dis, Nanning 530011, Peoples R China
Liang, Jian
[1
]
机构:
[1] Guangxi Univ Chinese Med, Ruikang Hosp, Dept Infect Dis, Nanning 530011, Peoples R China
来源:
VIROLOGY JOURNAL
|
2015年
/
12卷
基金:
中国国家自然科学基金;
关键词:
Sparstolonin B;
HIV transcription;
TAR region;
IMMUNODEFICIENCY-VIRUS TYPE-1;
TAR RNA;
LYMPHOCYTES;
REPLICATION;
ACTIVATION;
UPSTREAM;
SYNERGY;
INVITRO;
BINDING;
D O I:
10.1186/s12985-015-0339-8
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Background: The Chines herb derived Sparstolonin B, (SsnB), is a recently identified natural compound that selectively blocks TLR2- and TLR4-mediated inflammatory signaling. But it is unknown whether this compound has any effect on HIV infection. Findings: We found that SsnB treatment blocked HIV-1 transcription via a novel mechanism that requires the TAR region. Treatment of human T cell lines or peripheral blood mononuclear cells with SsnB at 1 mu M significantly inhibited HIV production. Lastly, SsnB was able to inhibit HIV in synergy with AZT. Conclusions: These data suggest that SsnB is a novel natural compound that inhibits HIV-1 transcription and may be a new drug in the treatment of HIV infection.
机构:
Mem Sloan Kettering Canc Ctr, Mol Pharmacol & Chem Program, Preclin Pharmacol Core Lab, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Mol Pharmacol & Chem Program, Preclin Pharmacol Core Lab, New York, NY 10021 USA
机构:
Mem Sloan Kettering Canc Ctr, Mol Pharmacol & Chem Program, Preclin Pharmacol Core Lab, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Mol Pharmacol & Chem Program, Preclin Pharmacol Core Lab, New York, NY 10021 USA