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Immunoelectron microscopic localization of HLA-DR antigen in control small intestine and colon and in inflammatory bowel disease

dc.contributor.authorHirata, Ichiroen_US
dc.contributor.authorAustin, Linda Leeen_US
dc.contributor.authorBlackwell, Walter H.en_US
dc.contributor.authorWeber, John R.en_US
dc.contributor.authorDobbins, William O. IIIen_US
dc.date.accessioned2006-09-11T14:44:41Z
dc.date.available2006-09-11T14:44:41Z
dc.date.issued1986-12en_US
dc.identifier.citationHirata, Ichiro; Austin, Linda L.; Blackwell, Walter H.; Weber, John R.; Dobbins, William O.; (1986). "Immunoelectron microscopic localization of HLA-DR antigen in control small intestine and colon and in inflammatory bowel disease." Digestive Diseases and Sciences 31(12): 1317-1330. <http://hdl.handle.net/2027.42/44398>en_US
dc.identifier.issn0163-2116en_US
dc.identifier.issn1573-2568en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/44398
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3542442&dopt=citationen_US
dc.description.abstractWe have elucidated the distribution of I2 (HLA-DR) antigen in control and inflammatory bowel disease specimens, using immunoelectron microscopic methods. Control small intestinal epithelium and inflammatory bowel disease epithelium expressed I2 antigen, while control colonic epithelium did not. I2 expression by enterocytes was more frequent on the lateral and basal surface than on the microvillus surface. Two of three M cells in control ileum expressed I2 antigen. I2-positive intraepithelial lymphocytes were rarely detected in both control and disease specimens. I2-positive lamina propria lymphocytes were significantly increased in inflammatory bowel disease, while I2-positive lamina propria lymphocytes were virtually absent in control specimens. I2-positive mononuclear cells in the intestinal lamina propria were largely macrophages and monocytes in both control and inflammatory bowel disease specimens. I2-positive mononuclear cells resembling dendritic cells were not detected in control or disease specimens. Furthermore, there were no significant morphological differences in I2-positive or-negative macrophages and monocytes in control and disease specimens. The expression of I2 antigen on Schwann cells was detected more frequently in disease specimens than in control specimens. Capillary endothelia of both control and disease specimens expressed I2 antigen. We demonstrate that I2 expression is present on surface membranes of both immune and nonimmune cells of the intestine and colon and show that this expression is more prominent in inflammatory bowel disease than in control intestine and colon. Further studies are required to determine whether this finding is meaningful in terms of antigen presentation and whether this apparent “immune activation” is involved in the pathogenesis of inflammatory bowel disease.en_US
dc.format.extent5713809 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.otherMedicine & Public Healthen_US
dc.subject.otherGastroenterologyen_US
dc.subject.otherHepatologyen_US
dc.subject.otherOncologyen_US
dc.subject.otherTransplant Surgeryen_US
dc.subject.otherBiochemistry, Generalen_US
dc.titleImmunoelectron microscopic localization of HLA-DR antigen in control small intestine and colon and in inflammatory bowel diseaseen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartments of Internal Medicine, University of Michigan Medical School, 2215 Fuller Road, 48105, Ann Arbor, Michigan; Veterans Administration Medical Center, 2215 Fuller Road, 48105, Ann Arbor, Michigan; The 2nd Division of Internal Medicine, Osaka Medical College, 2-7 Daigaku-machi, Takatsuki Osaka, Japanen_US
dc.contributor.affiliationumDepartments of Internal Medicine, University of Michigan Medical School, 2215 Fuller Road, 48105, Ann Arbor, Michigan; Veterans Administration Medical Center, 2215 Fuller Road, 48105, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartments of Internal Medicine, University of Michigan Medical School, 2215 Fuller Road, 48105, Ann Arbor, Michigan; Veterans Administration Medical Center, 2215 Fuller Road, 48105, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartments of Internal Medicine, University of Michigan Medical School, 2215 Fuller Road, 48105, Ann Arbor, Michigan; Veterans Administration Medical Center, 2215 Fuller Road, 48105, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartments of Internal Medicine, University of Michigan Medical School, 2215 Fuller Road, 48105, Ann Arbor, Michigan; Veterans Administration Medical Center, 2215 Fuller Road, 48105, Ann Arbor, Michiganen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid3542442en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/44398/1/10620_2005_Article_BF01299810.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF01299810en_US
dc.identifier.sourceDigestive Diseases and Sciencesen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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