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pubmed-article:1279206pubmed:abstractTextLevels of human immunodeficiency virus (HIV) DNA, RNA, or p24 antigen and reverse transcriptase activity in T-cell cultures treated with 500 IU of recombinant alpha interferon (rIFN alpha) per ml were comparable to those in control cultures. Radioimmunoprecipitation analysis of proteins in lysates of IFN-treated T cells documented a marked accumulation of HIV proteins. Localization of gp120 by immunofluorescence showed a diffuse pattern in IFN-treated cells quite distinct from the ring pattern in untreated control cells. That large quantities of gp120 in aberrant cell compartments might affect HIV morphogenesis was confirmed in infectivity studies: virions from IFN-treated cells were 100- to 1,000-fold less infectious than an equal number of virions from control cells. Direct examination of IFN-treated and control HIV-infected cells by transmission electron microscopy showed little difference in the number or distribution of viral particles. However, quantitation of gp120 by immunogold particle analysis revealed a marked depletion of envelope glycoprotein in virions released from IFN-treated cells. This defect in gp120 assembly onto mature viral particles provides a molecular basis for this loss of infectivity.lld:pubmed
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pubmed-article:1279206pubmed:articleTitleLoss of infectivity by progeny virus from alpha interferon-treated human immunodeficiency virus type 1-infected T cells is associated with defective assembly of envelope gp120.lld:pubmed
pubmed-article:1279206pubmed:affiliationDepartment of Cellular Immunology, Walter Reed Army Institute of Research, Washington, D.C. 20307-5100.lld:pubmed
pubmed-article:1279206pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1279206pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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