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dc.contributor.authorKoup, Richard A.
dc.contributor.authorSullivan, John L.
dc.contributor.authorLevine, Peter H.
dc.contributor.authorBrewster, Frank E.
dc.contributor.authorMahr, Anna
dc.contributor.authorMazzara, Gail
dc.contributor.authorMcKenzie, Sara
dc.contributor.authorPanicali, Dennis
dc.date2022-08-11T08:09:34.000
dc.date.accessioned2022-08-23T16:36:12Z
dc.date.available2022-08-23T16:36:12Z
dc.date.issued1989-02-01
dc.date.submitted2009-03-26
dc.identifier.citationJ Virol. 1989 Feb;63(2):584-90.
dc.identifier.issn0022-538X (Print)
dc.identifier.pmid2536094
dc.identifier.urihttp://hdl.handle.net/20.500.14038/38734
dc.description.abstractAntibody-dependent cell-mediated cytotoxicity (ADCC) specific for human immunodeficiency virus (HIV) has been described for HIV-infected individuals. To determine the antigenic specificity of this immune response and to define its relationship to the disease state, an ADCC assay was developed using Epstein-Barr virus-transformed lymphoblastoid cell line targets infected with vaccinia virus vectors expressing HIV proteins. The vaccinia virus vectors induced appropriate HIV proteins (envelope glycoproteins gp160, gp120, and gp41 or gag proteins p55, p40, p24, and p17) in infected lymphoblastoid cell lines as demonstrated by radioimmunoprecipitation and syncytia formation with c8166 cells. Killer cell-mediated, HIV-specific ADCC was found in sera from HIV-seropositive but not HIV-seronegative hemophiliacs. This HIV-specific response was directed against envelope glycoprotein but was completely absent against target cells expressing the HIV gag proteins. The ADCC directed against gp160 was present at serum dilutions up to 1/316,000. There was no correlation between serum ADCC titer and the stage of HIV-related illness as determined by T-helper-cell numbers. These experiments clearly implicated gp160 as the target antigen of HIV-specific ADCC activity following natural infection. Vaccines which stimulate antibodies directed against gp160, which are capable of mediating ADCC against infected cells, could be important for protection against infection by cell-associated virus.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=2536094&dopt=Abstract">Link to Article in PubMed</a>
dc.subject*Antibody-Dependent Cell Cytotoxicity
dc.subjectHIV
dc.subjectHIV Antibodies
dc.subjectHIV Antigens
dc.subjectHIV Envelope Protein gp120
dc.subjectHIV Envelope Protein gp41
dc.subjectHIV Seropositivity
dc.subjectHemophilia A
dc.subjectHumans
dc.subjectKiller Cells, Natural
dc.subjectRetroviridae Proteins
dc.subjectViral Envelope Proteins
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleAntigenic specificity of antibody-dependent cell-mediated cytotoxicity directed against human immunodeficiency virus in antibody-positive sera
dc.typeJournal Article
dc.source.journaltitleJournal of virology
dc.source.volume63
dc.source.issue2
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2584&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/1585
dc.identifier.contextkey798563
refterms.dateFOA2022-08-23T16:36:12Z
html.description.abstract<p>Antibody-dependent cell-mediated cytotoxicity (ADCC) specific for human immunodeficiency virus (HIV) has been described for HIV-infected individuals. To determine the antigenic specificity of this immune response and to define its relationship to the disease state, an ADCC assay was developed using Epstein-Barr virus-transformed lymphoblastoid cell line targets infected with vaccinia virus vectors expressing HIV proteins. The vaccinia virus vectors induced appropriate HIV proteins (envelope glycoproteins gp160, gp120, and gp41 or gag proteins p55, p40, p24, and p17) in infected lymphoblastoid cell lines as demonstrated by radioimmunoprecipitation and syncytia formation with c8166 cells. Killer cell-mediated, HIV-specific ADCC was found in sera from HIV-seropositive but not HIV-seronegative hemophiliacs. This HIV-specific response was directed against envelope glycoprotein but was completely absent against target cells expressing the HIV gag proteins. The ADCC directed against gp160 was present at serum dilutions up to 1/316,000. There was no correlation between serum ADCC titer and the stage of HIV-related illness as determined by T-helper-cell numbers. These experiments clearly implicated gp160 as the target antigen of HIV-specific ADCC activity following natural infection. Vaccines which stimulate antibodies directed against gp160, which are capable of mediating ADCC against infected cells, could be important for protection against infection by cell-associated virus.</p>
dc.identifier.submissionpathoapubs/1585
dc.contributor.departmentDepartment of Medicine
dc.contributor.departmentDepartment of Pediatrics
dc.source.pages584-90


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