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Development and applications of a monoclonal antibody against caprine interferon-gamma
BACKGROUND: Interferon-gamma (IFN-γ) is an important mediator of type I immune response and has antiviral, immunoregulatory and anti-tumor properties, plays a wide range of roles in inflammation and autoimmune diseases. The aim of this study was to obtain monoclonal antibody (mAb) against caprine IF...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929374/ https://www.ncbi.nlm.nih.gov/pubmed/31870349 http://dx.doi.org/10.1186/s12896-019-0596-5 |
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author | Ma, Wen-Tao Liu, Qi Ning, Meng-Xia Qi, Yu-Xu Rehman, Saad Chen, De-Kun |
author_facet | Ma, Wen-Tao Liu, Qi Ning, Meng-Xia Qi, Yu-Xu Rehman, Saad Chen, De-Kun |
author_sort | Ma, Wen-Tao |
collection | PubMed |
description | BACKGROUND: Interferon-gamma (IFN-γ) is an important mediator of type I immune response and has antiviral, immunoregulatory and anti-tumor properties, plays a wide range of roles in inflammation and autoimmune diseases. The aim of this study was to obtain monoclonal antibody (mAb) against caprine IFN-γ by immunizing of BALB/c mice with the purified rIFN-γ. RESULTS: Recombinant caprine IFN-γ was expressed in Escherichia coli strain BL21 (DE3) and monoclonal antibodies against caprine IFN-γ were produced by immunizing of BALB/c mice with rIFN-γ. One hybridoma secreting mAb was screened by enzyme-linked immunosorbent assay (ELISA) which was designated as 2C. MAb secreted by this cell line were analyzed through ELISA, western blot and application of the mAb was evaluated by immunofluorescence analysis using goat lip tissues infected with Orf virus. ELISA analysis revealed that mAb 2C can specifically recognize rIFN-γ protein and culture supernatant of goat peripheral blood mononuclear cells (PBMCs) stimulated by concanavalin A (Con A) but cannot recognize the fusion tag protein of pET-32a. Western blot analysis showed that mAb 2C can specifically react with the purified 34.9 kDa rIFN-γ protein but does not react with the fusion tag protein of pET-32a. Immunofluorescence results demonstrated that mAb 2C can detect IFN-γ secreted in histopathological sites of goats infected with Orf virus. CONCLUSIONS: A caprine IFN-γ-specific mAb was successfully developed in this study. Further analyses showed that the mAb can be used to detect IFN-γ expression level during contagious ecthyma in goats. |
format | Online Article Text |
id | pubmed-6929374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69293742019-12-30 Development and applications of a monoclonal antibody against caprine interferon-gamma Ma, Wen-Tao Liu, Qi Ning, Meng-Xia Qi, Yu-Xu Rehman, Saad Chen, De-Kun BMC Biotechnol Research Article BACKGROUND: Interferon-gamma (IFN-γ) is an important mediator of type I immune response and has antiviral, immunoregulatory and anti-tumor properties, plays a wide range of roles in inflammation and autoimmune diseases. The aim of this study was to obtain monoclonal antibody (mAb) against caprine IFN-γ by immunizing of BALB/c mice with the purified rIFN-γ. RESULTS: Recombinant caprine IFN-γ was expressed in Escherichia coli strain BL21 (DE3) and monoclonal antibodies against caprine IFN-γ were produced by immunizing of BALB/c mice with rIFN-γ. One hybridoma secreting mAb was screened by enzyme-linked immunosorbent assay (ELISA) which was designated as 2C. MAb secreted by this cell line were analyzed through ELISA, western blot and application of the mAb was evaluated by immunofluorescence analysis using goat lip tissues infected with Orf virus. ELISA analysis revealed that mAb 2C can specifically recognize rIFN-γ protein and culture supernatant of goat peripheral blood mononuclear cells (PBMCs) stimulated by concanavalin A (Con A) but cannot recognize the fusion tag protein of pET-32a. Western blot analysis showed that mAb 2C can specifically react with the purified 34.9 kDa rIFN-γ protein but does not react with the fusion tag protein of pET-32a. Immunofluorescence results demonstrated that mAb 2C can detect IFN-γ secreted in histopathological sites of goats infected with Orf virus. CONCLUSIONS: A caprine IFN-γ-specific mAb was successfully developed in this study. Further analyses showed that the mAb can be used to detect IFN-γ expression level during contagious ecthyma in goats. BioMed Central 2019-12-23 /pmc/articles/PMC6929374/ /pubmed/31870349 http://dx.doi.org/10.1186/s12896-019-0596-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Ma, Wen-Tao Liu, Qi Ning, Meng-Xia Qi, Yu-Xu Rehman, Saad Chen, De-Kun Development and applications of a monoclonal antibody against caprine interferon-gamma |
title | Development and applications of a monoclonal antibody against caprine interferon-gamma |
title_full | Development and applications of a monoclonal antibody against caprine interferon-gamma |
title_fullStr | Development and applications of a monoclonal antibody against caprine interferon-gamma |
title_full_unstemmed | Development and applications of a monoclonal antibody against caprine interferon-gamma |
title_short | Development and applications of a monoclonal antibody against caprine interferon-gamma |
title_sort | development and applications of a monoclonal antibody against caprine interferon-gamma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929374/ https://www.ncbi.nlm.nih.gov/pubmed/31870349 http://dx.doi.org/10.1186/s12896-019-0596-5 |
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