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pubmed-article:8892897pubmed:abstractTextThe enzymatic activity of the human immunodeficiency type 1 (HIV-1) protease (PR) is crucial to render HIV-1 virions mature and infectious. Hence, genetic intervention strategies based on trans-dominant (td) variants of the HIV-1 PR might be an alternative to current pharmacological and gene therapy regimens for AIDS. CD4-positive human CEM-SS T-cell lines were generated which constitutively expressed HIV-1 td PR variants. HIV-1 infection experiments demonstrated severely reduced HIV-1 replication in these td PR CEM-SS cell lines compared with control T cells expressing wild-type PR. Furthermore, replication of an HIV-1 isolate bearing a PR inhibitor-resistant PR was blocked, showing that genetic intervention strategies based on td PRs can be effective against HIV-1 isolates containing PR inhibitor-resistant mutants.lld:pubmed
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pubmed-article:8892897pubmed:dateRevised2009-11-18lld:pubmed
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pubmed-article:8892897pubmed:articleTitleIntracellular expression of human immunodeficiency virus type 1 (HIV-1) protease variants inhibits replication of wild-type and protease inhibitor-resistant HIV-1 strains in human T-cell lines.lld:pubmed
pubmed-article:8892897pubmed:affiliationProgenesys Program at Systemix, Palo Alto, California 94304, USA.lld:pubmed
pubmed-article:8892897pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8892897pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:8892897pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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