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The effect of 6-mercaptopurine on natural killer-cell activities in Crohn's disease

dc.contributor.authorKorelitz, B.en_US
dc.contributor.authorOliver, M.en_US
dc.contributor.authorBrogan, M.en_US
dc.contributor.authorHiserodt, J. C.en_US
dc.contributor.authorStevens, R.en_US
dc.contributor.authorTargan, S.en_US
dc.date.accessioned2006-09-11T15:21:10Z
dc.date.available2006-09-11T15:21:10Z
dc.date.issued1985-05en_US
dc.identifier.citationBrogan, M.; Hiserodt, J.; Oliver, M.; Stevens, R.; Korelitz, B.; Targan, S.; (1985). "The effect of 6-mercaptopurine on natural killer-cell activities in Crohn's disease." Journal of Clinical Immunology 5(3): 204-211. <http://hdl.handle.net/2027.42/44846>en_US
dc.identifier.issn1573-2592en_US
dc.identifier.issn0271-9142en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/44846
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3874211&dopt=citationen_US
dc.description.abstractCrohn's disease patients on long-term 6-mercaptopurine therapy (more than 4 months) were evaluated for activity of peripheral blood natural killer cells. Natural killer-cell cytolytic activity against K-562 tumor-cell targets was examined, as was natural killer-cell suppression of lymphoblastoid B-cell antibody production. In addition, these patients were studied for their ability to generate antitetanus-specific IgG antibody-producing lymphoblastoid B cells following in vivo booster immunization. Crohn's disease patients on 6-mercaptopurine therapy had significant reductions in peripheral blood natural killer-cell activity against K-562 targets compared to normals, disease controls, and Crohn's disease patients not on 6-mercaptopurine. Natural killer-cell suppression of lymphoblastoid B-cell antibody production was like-wise decreased in 6-mercaptopurine-treated patients compared to normal controls. In contrast, the in vivo generated lymphoblastoid B-cell antibody responses of Crohn's disease patients on 6-mercaptopurine therapy were not decreased compared to normal, while Crohn's disease patients not on 6-mercaptopurine therapy had significantly impaired IgG antitetanus antibody responses. These findings suggest that 6-mercaptopurine therapy in Crohn's disease affects several lymphoid subpopulations, resulting in a decreased natural killer-cell cytotoxic activity against K-562 target cells and a decreased natural killer-cell ability to suppress lymphoblastoid B-cell antibody production, as well as an improved humoral immune response following tetanus toxoid booster immunization.en_US
dc.format.extent924673 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers-Plenum Publishers; Plenum Publishing Corporation ; Springer Science+Business Mediaen_US
dc.subject.otherImmunologyen_US
dc.subject.otherCrohn's Diseaseen_US
dc.subject.other6-Mercaptopurineen_US
dc.subject.otherBiomedicineen_US
dc.subject.otherMedical Microbiologyen_US
dc.subject.otherInternal Medicineen_US
dc.subject.otherInfectious Diseasesen_US
dc.subject.otherNatural Killer Cellsen_US
dc.subject.otherSuppressor Cellsen_US
dc.subject.otherAntibody-producing Cellsen_US
dc.titleThe effect of 6-mercaptopurine on natural killer-cell activities in Crohn's diseaseen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMicrobiology and Immunologyen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pathology, University of Michigan Medical Center, 48105, Ann Arbor, Michiganen_US
dc.contributor.affiliationotherDepartment of Medicine, Microbiology and Immunology, UCLA School of Medicine, V.A. Wadsworth Medical Center, 90024, Los Angeles, Californiaen_US
dc.contributor.affiliationotherDepartment of Medicine, Microbiology and Immunology, UCLA School of Medicine, V.A. Wadsworth Medical Center, 90024, Los Angeles, Californiaen_US
dc.contributor.affiliationotherDepartment of Medicine, Microbiology and Immunology, UCLA School of Medicine, V.A. Wadsworth Medical Center, 90024, Los Angeles, Californiaen_US
dc.contributor.affiliationotherDepartment of Gastroenterology, Lennox Hill Hospital, 10021, New York, New Yorken_US
dc.contributor.affiliationotherDepartment of Medicine, Microbiology and Immunology, UCLA School of Medicine, V.A. Wadsworth Medical Center, 90024, Los Angeles, California; Department of Medicine, Center for the Health Sciences, UCLA School of Medicine, 90024, Los Angeles, Californiaen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid3874211en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/44846/1/10875_2004_Article_BF00915512.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00915512en_US
dc.identifier.sourceJournal of Clinical Immunologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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