Volume 73, Issue 7 (October 2015)                   Tehran Univ Med J 2015, 73(7): 535-539 | Back to browse issues page

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Zamani S, Fotouhi Chahouki F, Nourmohammadi Z, Sadeghi Neshat S, Mazaheri V, Torabi A et al . Production of polyclonal antibody against Tehran strain influenza virus (A/H1N1/2009) hemagglutinin conserved domain (HA2): brief report. Tehran Univ Med J. 2015; 73 (7) :535-539
URL: http://tumj.tums.ac.ir/article-1-6915-en.html
1- Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
2- Department of Virology, Influenza Research Lab, Pasteur Institute of Iran, Tehran, Iran.
3- Department of Virology, Influenza Research Lab, Pasteur Institute of Iran, Tehran, Iran. , b_farahmand@pasteur.ac.ir
Abstract:   (3714 Views)

Background: The influenza virus is one of the most important factors for higher morbidity and mortality in the world. Recently, researchers have been focused on influenza conserved antigenic proteins such as hemagglutinin stalk domain (HA2) for vaccine production and serological studies. The HA2 plays a major role in the fusion of the virus with host cells membrane. The immunity system enables to produce antibody against HA2. The aim of this study is polyclonal antibody production against influenza HA2. Methods: This study was done in the Influenza Research Lab, Pasteur Institute of Iran, Tehran for one year from September 2013 to October 2014. In the present study, recombinant HA2 protein was produced in prokaryotic system and purified using Nickel affinity chromatography. The purified HA2 was mixed with Freund’s adjuvant (complete and incomplete) and injected into two New Zealand white rabbits by intramuscularly and subcutaneously routes. Immunization was continued for several months with two weeks interval. Before each immunization, blood was drawn by venous puncture from the rabbit ear. Function of rabbitchr('39')s sera was evaluated using radial immunodiffusion (RID) in both forms, Single RID (SRID) and Double RID (DRID). Finally, antiserum activity against HA2 was evaluated using western blotting as serological assay. Results: Sedimentary line and zone was observed in RID assays (SRID and DRID) represent interaction between HA2 protein and anti- HA2 antibody. As well as, western blotting results was positive for HA2 protein. Therefore, these results showed that polyclonal antibody produced against HA2 protein can identify HA2 protein antigenic sites. Conclusion: These findings show that humoral immune responses have properly been stimulated in rabbits and these antibodies can identify HA2 protein and may be suitable for other serological methods.

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Type of Study: Brief Report |

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