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Increased thymic hormone responsive suppressor T lymphocyte function in chronic active hepatitis

dc.contributor.authorMutchnick, Milton G.en_US
dc.contributor.authorSchaffner, John A.en_US
dc.contributor.authorPrieto, Jorge A.en_US
dc.contributor.authorWeller, Frederick E.en_US
dc.contributor.authorGoldstein, Allan L.en_US
dc.date.accessioned2006-09-11T14:44:14Z
dc.date.available2006-09-11T14:44:14Z
dc.date.issued1983-04en_US
dc.identifier.citationMutchnick, Milton G.; Schaffner, John A.; Prieto, Jorge A.; Weller, Frederick E.; Goldstein, Allan L.; (1983). "Increased thymic hormone responsive suppressor T lymphocyte function in chronic active hepatitis." Digestive Diseases and Sciences 28(4): 328-334. <http://hdl.handle.net/2027.42/44394>en_US
dc.identifier.issn0163-2116en_US
dc.identifier.issn1573-2568en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/44394
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=6219866&dopt=citationen_US
dc.description.abstractMitogen-induced suppressor T lymphocyte function was evaluated in patients with chronic active hepatitis (CAH). The in vitro effect of the biological response modifier, thymosin fraction 5, on the suppressive activity of peripheral blood mononuclear cells (PBM) was also assessed. Suppressor cell activity was significantly decreased in patients with CAH when compared to controls ( P <0.001). In the absence of the inducing mitogen, thymosin-treated PBM from both patients and controls promoted enhancement of tritiated thymidine uptake by cocultured allogeneic lymphocytes. When thymosin-treated mononuclear cells were mitogen-activated; patients, but not the controls, showed a marked increase in suppressor activity ( P <0.001). These results indicate that the polypeptides contained in thymosin fraction 5 can promote a helper effect in patients and controls. Furthermore, PBM from patients with CAH contain a subset of lymphocytes that can express a suppressive function following thymosin treatment. We conclude that thymosin fraction 5 can promote an in vitro restoration of suppressor T cell function in patients with CAH.en_US
dc.format.extent686173 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers-Plenum Publishers; Digestive Disease Systems, Inc. ; Springer Science+Business Mediaen_US
dc.subject.otherHepatologyen_US
dc.subject.otherMedicine & Public Healthen_US
dc.subject.otherGastroenterologyen_US
dc.subject.otherOncologyen_US
dc.subject.otherTransplant Surgeryen_US
dc.subject.otherBiochemistry, Generalen_US
dc.titleIncreased thymic hormone responsive suppressor T lymphocyte function in chronic active hepatitisen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Medicine, University of Michigan Medical Center, Ann Arbor, Michigan; Department of Medicine, Ann Arbor V.A. Medical Center, 2215 Fuller Road, 48105, Ann Arbor, Michigan; Department of Biochemistry, The George Washington University School of Medicine and Health Sciences, Washington, DCen_US
dc.contributor.affiliationumDepartment of Medicine, University of Michigan Medical Center, Ann Arbor, Michigan; Department of Medicine, Ann Arbor V.A. Medical Center, 2215 Fuller Road, 48105, Ann Arbor, Michigan; Department of Biochemistry, The George Washington University School of Medicine and Health Sciences, Washington, DCen_US
dc.contributor.affiliationumDepartment of Medicine, University of Michigan Medical Center, Ann Arbor, Michigan; Department of Medicine, Ann Arbor V.A. Medical Center, 2215 Fuller Road, 48105, Ann Arbor, Michigan; Department of Biochemistry, The George Washington University School of Medicine and Health Sciences, Washington, DCen_US
dc.contributor.affiliationumDepartment of Medicine, University of Michigan Medical Center, Ann Arbor, Michigan; Department of Medicine, Ann Arbor V.A. Medical Center, 2215 Fuller Road, 48105, Ann Arbor, Michigan; Department of Biochemistry, The George Washington University School of Medicine and Health Sciences, Washington, DCen_US
dc.contributor.affiliationumDepartment of Medicine, University of Michigan Medical Center, Ann Arbor, Michigan; Department of Medicine, Ann Arbor V.A. Medical Center, 2215 Fuller Road, 48105, Ann Arbor, Michigan; Department of Biochemistry, The George Washington University School of Medicine and Health Sciences, Washington, DCen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid6219866en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/44394/1/10620_2005_Article_BF01324949.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF01324949en_US
dc.identifier.sourceDigestive Diseases and Sciencesen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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