Characterization of a Novel Anti-DR5 Monoclonal Antibody WD1 with the Potential to Induce Tumor Cell Apoptosis

TNF-related apoptosis-inducing ligand (TRAIL) is a TNF family member capable of inducing apoptosis. Death receptor 5 (DR 5) is a key receptor of TRAIL and plays an important role in TRAIL-induced apoptosis. To prepare monoclonal antibodies (mAbs) against DR5, cDNA encoding soluble DR5 (sDR5) was fir...

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Published inCellular & molecular immunology Vol. 5; no. 1; pp. 55 - 60
Main Authors Wang, Jing, Lin, Zhou, Qiao, Chunxia, Lv, Ming, Yu, Ming, Xiao, He, Wang, Qingyang, Wang, Liyan, Feng, Jiannan, Shen, Beifen, Ma, Yangfang, Li, Yan
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.02.2008
Nature Publishing Group
These authors contributed equally to this work%Institute of Basic Medical Sciences, Beijing, China%Laboratory of Cellular and Molecular Immunology, Institute of Immunology, Henan University, Kaifeng, China
These authors contributed equally to this work%Institute of Basic Medical Sciences, Beijing, China
Laboratory of Cellular and Molecular Immunology, Institute of Immunology, Henan University, Kaifeng, China
Institute of Basic Medical Sciences, Beijing, China%Laboratory of Cellular and Molecular Immunology, Institute of Immunology, Henan University, Kaifeng, China
Laboratory of Cellular and Molecular Immunology, Institute of Immunology, Henan University, Kaifeng 475001, China%Laboratory of Cellular and Molecular Immunology, Institute of Immunology, Henan University, Kaifeng, China
Laboratory of Cellular and Molecular Immunology, Institute of Immunology, Henan University, Kaifeng 475001, China
Institute of Basic Medical Sciences, Beijing, China
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Summary:TNF-related apoptosis-inducing ligand (TRAIL) is a TNF family member capable of inducing apoptosis. Death receptor 5 (DR 5) is a key receptor of TRAIL and plays an important role in TRAIL-induced apoptosis. To prepare monoclonal antibodies (mAbs) against DR5, cDNA encoding soluble DR5 (sDR5) was firstly amplified by reverse transcriptase-polymerase chain reaction (RT-PCR) with specific primers, and then inserted into a prokaryotic expression vector pET-30a. The recombinant plasmid was expressed in Escherichia coli strain BL21 (DE3), and sDR5 was purified by nickel affinity chromatography. As an antigen, sDR5 was used to immunize mice. Hybridomas secreting antibodies against sDR5 were identified. One positive done was selected to produce antibody, WD1. ELISA and immunofluorescence demonstrated that WD1 could bind recombinant sDR5 and membranebound DR5 (mDR5) on Jurkat and Molt-4 cells. ATPLite assays showed that Jurkat and Molt-4 cells were sensitive to the antibody in a dose dependent manner. The Annexin V/PI assays and Giemsa's staining both showed that WD1 could induce Jurkat cell apoptosis efficiently. Transient transfection of 293T cells and indirect immunofluorescence assay demonstrated that mAb (WD1) couldn't cross-react with DR4. Our findings indicated that the novel antibody, WD1 could act as a direct agonist, bind DR5 characteristically, and initiate efficient apoptotic signaling and tumor regression. Thus, WD1 would be a leading candidate for potential cancer therapeutics. Cellular & Molecular Immunology.
Bibliography:11-4987/R
R392
TRAIL, death receptor 5, apoptosis, monoclonal antibody, ATPLite
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These authors contributed equally to this work
ISSN:1672-7681
2042-0226
DOI:10.1038/cmi.2008.7