Immunological studies on chicken interferon-kappa using an antigen-capture ELISA developed using new mouse monoclonal antibodies

被引:6
|
作者
Lee, Youngsub [1 ]
Lu, Mingmin [1 ]
Lillehoj, Hyun S. [1 ]
机构
[1] USDA ARS, Anim Biosci & Biotechnol Lab, Beltsville Agr Res Ctr, Beltsville, MD 20705 USA
来源
DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY | 2021年 / 124卷
关键词
IFN-kappa; Type I IFNs; Capture ELISA; mRNA; Monoclonal antibody; I INTERFERON; STIMULATED GENES; CELLS; INDUCTION; VIRUS;
D O I
10.1016/j.dci.2021.104204
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Interferon (IFN)-kappa is a type I IFN that plays a central role in anti-viral defense and host immune response. The functions of type I IFNs have not been clearly defined in chickens compared to those of their mammalian counterparts. In this study, we developed an antigen-capture ELISA using newly developed mouse monoclonal antibodies (mAbs) which are specific for chicken IFN-kappa (chIFN-kappa) and showed that this ELISA can measure native chIFN-kappa production during the activation of macrophages by polyinosinic:polycytidylic acid (poly I:C). The recombinant chicken IFN-kappa expressed in Escherichia coli was used to immunize mice. Five mAbs that specifically recognized chIFN-kappa were selected and characterized based on their specificity and binding activity toward chIFN-kappa via indirect ELISA and western blotting. To develop a capture ELISA for chicken IFN-kappa, two sets of the best capture and detection mAbs combinations were identified via pairing assays. To validate the antigen-capture assay, the production of native IFN-kappa was induced in chicken HD11 macrophages using poly I:C. Furthermore, qRT-PCR was used to confirm the transcript-level expression of IFN-kappa in HD11 cells at 24 and 48 h. The neutralizing effects of anti-chIFN-kappa mAbs were evaluated based on their ability to block the induction of IFN-stimulated genes (ISGs) in DF-1 fibroblast cells stimulated with recombinant chIFN-kappa proteins. All five mAbs blocked the mRNA expression of ISGs in a dose-dependent manner. Our results validate the specificity and utility of these newly developed mAbs for the detection of native chicken IFN-kappa. This novel antigen-capture ELISA will be a valuable tool for fundamental and applied research involving IFN-kappa in the normal and diseased states.
引用
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页数:7
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