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pubmed-article:10235111pubmed:abstractTextHuman T-cell leukemia virus type I (HTLV-I) infection is emerging as an important complication in HIV infection and AIDS in injecting drug users. HIV-1 and HTLV-I share a common host in CD4+ T lymphocytes. However, the result of HIV-1 infection is the decimation of this cell population, whereas a hallmark of HTLV-I infection is the inappropriate proliferation of infected cells. Combined epidemiologic data suggest that HTLV-I infection is enhanced during concurrent HIV-1/HTLV-I infection; however, there are currently no in vitro studies focusing on the effects of drugs of abuse on retrovirus coinfection. We have found that in an in vitro coinfection system (HIV-1 + HTLV-I), morphine treatment further enhanced the levels of HTLV-I p19. In addition, indicators of in vitro infection by cell-free HIV-1 were reduced by morphine treatment in both single and dual in vitro infection experiments. Interleukin 2 levels in the affected cultures were found to increase with combined HTLV-I infection and morphine treatment. These in vitro results indicate the need to further explore the activity of HTLV-I within opiate-treated cells, as this oncoretrovirus appears to be especially sensitive to morphine-induced alterations to its host cell environment.lld:pubmed
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pubmed-article:10235111pubmed:authorpubmed-author:UgenK EKElld:pubmed
pubmed-article:10235111pubmed:authorpubmed-author:NylandS BSBlld:pubmed
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pubmed-article:10235111pubmed:volume18lld:pubmed
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pubmed-article:10235111pubmed:pagination285-91lld:pubmed
pubmed-article:10235111pubmed:dateRevised2007-11-15lld:pubmed
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pubmed-article:10235111pubmed:articleTitleMorphine effects on HTLV-I infection in the presence or absence of concurrent HIV-1 infection.lld:pubmed
pubmed-article:10235111pubmed:affiliationDepartment of Medical Microbiology and Immunology, University of South Florida College of Medicine, Tampa 33612, USA.lld:pubmed
pubmed-article:10235111pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:10235111pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed