Publication:
Production and characterization of monoclonal antibodies against major histocompatibility complex class I chain-related gene A

dc.contributor.authorW. Wongsenaen_US
dc.contributor.authorG. Sconocchiaen_US
dc.contributor.authorH. S. Choen_US
dc.contributor.authorC. C. Changen_US
dc.contributor.authorX. Wangen_US
dc.contributor.authorK. Klumkrathoken_US
dc.contributor.authorS. Ferroneen_US
dc.contributor.authorC. Leelayuwaten_US
dc.contributor.otherKhon Kaen Universityen_US
dc.contributor.otherRoswell Park Cancer Instituteen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherUniversitat Baselen_US
dc.contributor.otherUniversity of Pittsburghen_US
dc.date.accessioned2018-07-12T02:16:47Z
dc.date.available2018-07-12T02:16:47Z
dc.date.issued2008-11-01en_US
dc.description.abstractMajor histocompatibility complex (MHC) class I chain-related gene A (MICA), a ligand for the activating immunoreceptor natural killer group 2D (NKG2D), is expressed on stressed cells such as tumor cells. Study of expression of this molecule on tumor cells and patients' sera is useful to define patients' stages leading to proper selection of therapy. In this study, mouse anti-MICA monoclonal antibodies (mAbs) were produced by DNA immunization using a gene gun. Screening of anti-MICA-producing mouse and hybridomas were performed by immunoblot and cell enzyme-linked immunosorbent assay (ELISA) against MICA-positive HeLa and -negative Me1386 cell lines. MAbs were characterized against MICA-positive and -negative cell lines by immunoblot, cell ELISA and flow cytometry. The mAbs were also characterized for locus and allele specificities of MICA and MHC class I chain-related gene B (MICB) as well as for their ability to stain formalin-fixed paraffin-embedded tissues by immunohistochemistry. Although all mouse immune sera were positive with MICA-positive cells by both immunoblot and cell ELISA methods, some hybridomas were positive only with one method. The mAbs had diverse specificities to detect MICA and MICB and different abilities to stain formalin-fixed paraffin-embedded tissues. Thus, DNA immunization by gene gun is an effective method to generate immune mice for the production of mAbs with a variety of specificities against native and denatured forms of MIC proteins. © 2008 The Authors.en_US
dc.identifier.citationTissue Antigens. Vol.72, No.5 (2008), 431-440en_US
dc.identifier.doi10.1111/j.1399-0039.2008.01118.xen_US
dc.identifier.issn13990039en_US
dc.identifier.issn00012815en_US
dc.identifier.other2-s2.0-54049123708en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/18839
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=54049123708&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleProduction and characterization of monoclonal antibodies against major histocompatibility complex class I chain-related gene Aen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=54049123708&origin=inwarden_US

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