Development of Monoclonal Antibodies Suitable for Rabies Virus Antibody and Antigen Detection

• Published in: Indian Journal of Virology Vol. 23; no. 3; pp. 317 - 325
• Main Authors: Chander, Vishal, Singh, R. P., Verma, P. C.
• Format: Journal Article
• Language: English
• Published: India Springer-Verlag 01.12.2012; Springer Nature B.V
• Subjects: Albinism; Antigens; Bats; Biochemistry; Biomedical and Life Sciences; Cell Biology; Cell culture; Central nervous system; Cloning; Enzyme-linked immunosorbent assay; Fluorescent antibody test; Genomes; Immunization; Indirect fluorescent antibody test; Life Sciences; Lyssavirus; Microbiology; Monoclonal antibodies; Multiple myeloma; Myeloma; Original; Original Article; Polyethylene glycol; Prophylaxis; Protein Structure; Proteins; Rabies; Titration; Vaccination; Vaccines; Viral diseases; Viruses; India; Antigen; Monoclonal antibody; Enzyme linked immunosorbent assay; Rabies virus
• DOI: 10.1007/s13337-012-0096-x
• ISSN: 0970-2822; 2347-3584

The control of an infectious viral disease as rabies is made easier by rapid and accurate diagnosis. Successful rabies prophylaxis is dependent upon the active immunization with vaccine along with passive administration of rabies virus neutralizing antibodies which together clear the virus before widespread infection of central nervous system occurs. The present study aimed at the development of monoclonal antibodies (MAbs) suitable for rabies virus antibody and antigen detection. For the production of rabies specific MAbs, immunization of Swiss albino mice with a commercially available vaccine was done and Polyethylene glycol mediated fusion of spleenocytes with myeloma cells was performed. The positive clones were selected on the basis of distinct reactivity by cell Enzyme linked immunosorbent assay and fluorescence in Indirect Fluorescent antibody test. The positive clones obtained were subjected to single cell cloning by limiting dilution method. The reactive clones were further titrated and employed for virus titration and virus neutralization. The neutralizing activity was evaluated using Fluorescence Activated Cell Sorter technique. Three MAb clones showed a distinct percent inhibition in the presence of positive serum. One of the MAb clone No. 5C3 was relatively more specific in detecting rabies antibodies and also found suitable for competitive ELISA to assess the antibody level in vaccinated subjects.