Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Ma, Wen-Tao, Liu, Qi, Ning, Meng-Xia, Qi, Yu-Xu, Rehman, Saad, Chen, De-Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
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
_version_ 1783482689451458560
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
work_keys_str_mv AT mawentao developmentandapplicationsofamonoclonalantibodyagainstcaprineinterferongamma
AT liuqi developmentandapplicationsofamonoclonalantibodyagainstcaprineinterferongamma
AT ningmengxia developmentandapplicationsofamonoclonalantibodyagainstcaprineinterferongamma
AT qiyuxu developmentandapplicationsofamonoclonalantibodyagainstcaprineinterferongamma
AT rehmansaad developmentandapplicationsofamonoclonalantibodyagainstcaprineinterferongamma
AT chendekun developmentandapplicationsofamonoclonalantibodyagainstcaprineinterferongamma