Research of Human-mouse Chimeric Antibodies Against Ebola Virus Nucleoprotein.
- Author:
Rongping ZHOU
;
Lina SUN
;
Yang LIU
;
Wei WU
;
Chuan LI
;
Mifang LIANG
;
Peihong QIU
- Publication Type:Journal Article
- MeSH:
Animals;
Antibodies, Monoclonal;
genetics;
immunology;
Cloning, Molecular;
Ebolavirus;
genetics;
immunology;
Hemorrhagic Fever, Ebola;
immunology;
virology;
Humans;
Immunoglobulin Heavy Chains;
genetics;
immunology;
Mice;
Nucleoproteins;
genetics;
immunology;
Viral Proteins;
genetics;
immunology
- From:
Chinese Journal of Virology
2016;32(1):14-18
- CountryChina
- Language:Chinese
-
Abstract:
The Ebola virus is highly infectious and can result in death in ≤ 90% of infected subjects. Detection of the Ebola virus and diagnosis of infection are extremely important for epidemic control. Presently, Chinese laboratories detect the nucleic acids of the Ebola virus by real-time reverse transcription-polymerase chain reaction (RT-PCR). However, such detection takes a relatively long time and necessitates skilled personnel and expensive equipment. Enzyme-linked immunosorbent assay (ELISA) of serum is simple, easy to operate, and can be used to ascertain if a patient is infected with the Ebola virus as well as the degree of infection. Hence, ELISA can be used in epidemiological investigations and is a strong complement to detection of nucleic acids. Cases of Ebola hemorrhagic fever have not been documented in China, so quality-control material for positive serology is needed. Construction and expression of human-mouse chimeric antibodies against the nucleoprotein of the Ebola virus was carried out. Genes encoding variable heavy (VH) and variable light (VL) chains were extracted and amplified from murine hybridoma cells. Genes encoding the VH and VL chains of monoclonal antibodies were amplified by RT-PCR. According to sequence analyses, a primer was designed to amplify functional sequences relative to VH and VL chain. The eukaryotic expression vector HL51-14 carrying some human antibody heavy chain- and light chain-constant regions was used. IgG antibodies were obtained by transient transfection of 293T cells. Subsequently, immunological detection and immunological identification were identified by ELISA, immunofluorescence assay, and western blotting. These results showed that we constructed and purified two human- mouse chimeric antibodies.
