Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
|
pubmed:dateCreated |
1995-3-23
|
pubmed:abstractText |
Recently, we have shown that in acutely infected T cells interferons (IFNs) effectively inhibit the human immunodeficiency type 1 (HIV-1) proviral DNA synthesis during a single replication cycle. In the present study, we have evaluated the relative effectiveness of IFNs in restricting HIV-1 expression at post-transcriptional level. Treatment of HeLa cells with IFNs A* and B (up to 1,000 U/ml) did not result in a reduction in HIV-1 RNA and protein synthesis encoded by the transfected HIV-1 proviral clone. Interestingly, IFN treatment reduced significantly the HIV-1 mRNA levels encoded by the transfected tat-defective HIV-1 provirus, and this inhibition could be overcome by transfection with Tat- and Rev-expressing plasmids. These results suggest that HIV-1-encoded Tat and Rev can overcome the inhibitory effects of IFNs on HIV-1 replication.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
0197-8357
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
14
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
259-63
|
pubmed:dateRevised |
2007-11-15
|
pubmed:meshHeading |
pubmed-meshheading:7532202-Gene Products, tat,
pubmed-meshheading:7532202-HIV-1,
pubmed-meshheading:7532202-HeLa Cells,
pubmed-meshheading:7532202-Humans,
pubmed-meshheading:7532202-Interferons,
pubmed-meshheading:7532202-RNA Processing, Post-Transcriptional,
pubmed-meshheading:7532202-Virus Replication,
pubmed-meshheading:7532202-tat Gene Products, Human Immunodeficiency Virus
|
pubmed:year |
1994
|
pubmed:articleTitle |
Modulation of interferon-mediated inhibition of human immunodeficiency virus type 1 by Tat.
|
pubmed:affiliation |
Oncology Center, Johns Hopkins University School of Medicine, Baltimore, MD 21231.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|