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Activation of human T cell clones through the UM4D4/CDw60 surface antigen

dc.contributor.authorFox, David A.en_US
dc.contributor.authorDavis, Williamen_US
dc.contributor.authorZeldes, Wendyen_US
dc.contributor.authorKan, Lien_US
dc.contributor.authorHiggs, Jayen_US
dc.contributor.authorDuby, Allan D.en_US
dc.contributor.authorHoloshitz, Josephen_US
dc.date.accessioned2006-04-10T13:41:43Z
dc.date.available2006-04-10T13:41:43Z
dc.date.issued1990-07en_US
dc.identifier.citationFox, David A., Davis, William, Zeldes, Wendy, Kan, Li, Higgs, Jay, Duby, Allan D., Holoshitz, Joseph (1990/07)."Activation of human T cell clones through the UM4D4/CDw60 surface antigen." Cellular Immunology 128(2): 480-489. <http://hdl.handle.net/2027.42/28512>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WCF-4F686TR-D/2/d8a22b2854bb181bbbce626b16b5e369en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/28512
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=2141550&dopt=citationen_US
dc.description.abstractUM4D4 is a recently defined antigen that is expressed on ~25% of peripheral blood T cells, but on the majority of T cells in inflammatory synovial fluid. Anti-UM4D4 activates peripheral blood T cells in the presence of accessory cells and/or phorbol ester. UM4D4 has been assigned to a new antigen cluster termed CDw60. The present study examined the ability of anti-UM4D4 to activate T cell clones derived from the synovial fluid of patients with rheumatoid arthritis. UM4D4 was expressed at varying levels on both lectin-generated and antigen-specific clones, including clones of CD4+, CD8+, and CD4-CD8- phenotypes. Anti-UM4D4 used in soluble form as a single stimulus was typically mitogenic for the CD4+ and some of the CD8+ clones, but not for the CD4-CD8- clones. Phorbol ester boosted the response to anti-UM4D4 in some clones, had no effect in others, and diminished the responses in some cases. In contrast to anti-UM4D4, anti-CD3 was generally not mitogenic in soluble form, although it was mitogenic when conjugated to beads. The data show that T cell clones derived from an inflammatory T cell infiltrate can be readily activated through the UM4D4/CDw60 antigen.en_US
dc.format.extent666190 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleActivation of human T cell clones through the UM4D4/CDw60 surface antigenen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Internal Medicine, Rackham Arthritis Research Unit, and Multipurpose Arthritis Center, University of Michigan, Ann Arbor, Michigan, U.S.A.en_US
dc.contributor.affiliationumDepartment of Internal Medicine, Rackham Arthritis Research Unit, and Multipurpose Arthritis Center, University of Michigan, Ann Arbor, Michigan, U.S.A.en_US
dc.contributor.affiliationumDepartment of Internal Medicine, Rackham Arthritis Research Unit, and Multipurpose Arthritis Center, University of Michigan, Ann Arbor, Michigan, U.S.A.en_US
dc.contributor.affiliationumDepartment of Internal Medicine, Rackham Arthritis Research Unit, and Multipurpose Arthritis Center, University of Michigan, Ann Arbor, Michigan, U.S.A.en_US
dc.contributor.affiliationumDepartment of Internal Medicine, Rackham Arthritis Research Unit, and Multipurpose Arthritis Center, University of Michigan, Ann Arbor, Michigan, U.S.A.en_US
dc.contributor.affiliationumDepartment of Medicine, Stanford University, Stanford, California, U.S.A.; Department of Internal Medicine, Rackham Arthritis Research Unit, and Multipurpose Arthritis Center, University of Michigan, Ann Arbor, Michigan, U.S.A.en_US
dc.contributor.affiliationotherHarold C. Simmons Arthritis Research Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas, U.S.A.en_US
dc.identifier.pmid2141550en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/28512/1/0000309.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0008-8749(90)90042-Pen_US
dc.identifier.sourceCellular Immunologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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