Fu Shi Quan, J <strong>Vaccines</strong> Vaccin <strong>2013</strong>, 4:5http://dx.doi.org/10.4172/2157-7560.S1.0163 rd International Conference on<strong>Vaccines</strong> & VaccinationJuly 29-31, <strong>2013</strong> Embassy Suites Las Vegas, NV, USA2009 H1N1 pandemic influenza virus-like particle vaccine efficacyFu Shi QuanDepartment of Medical Zoology, Kyung Hee University School of Medicine, Seoul, Korea 130-7012009 H1N1 pandemic influenza virus-like particles (VLPs) vaccine containing HA and M1 proteins derived from theA A/California/04/2009 virus was generated. The VLP vaccine efficacy was investigated for efficacy against homologous,heterogous and heterosubtypic influenza viruses in mice. A single intramuscular vaccination provided complete protection againsthomologous A/California/04/2009 viruses with no virus detected in lungs. For cross protective efficacy against antigenicallydistant H1N1 viruses, intramuscularly immunized mice were challenged with lethal dose of A/PR8/34 or A/Caledonia/99viruses after a 2 nd boost. Mice showed 100% protection against both viruses. Better cross protection against A/PR8/34 virusthan A/Caledonia/20/99 was characterized by lower lung virus titers, less body weight loss, and higher cross reactive recall IgGantibody secreting cell responses. For heterosubtypic immunity, intranasally immunized mice were challenged with lethal dosesof H3N2 viruses. Mice showed 100% survival with 10% to 16% body weight losses respectively against A/Philippine/82 or A/Hong Kong/68 challenge, whereas all naive control mice died. Mice showed higher cross reactive lung IgG and IgA responsesafter H3N2 virus challenges. These results indicate that VLPs can be developed as an effective vaccine which can confer protectionagainst homologous, heterogous and heterosubtypic influenza viruses.BiographyFu Shi Quan received her Ph.D. degree at Korea University Seoul, Korea and had postdoctoral training in the laboratory of Professor Richard W.Compans (Department of Microbiology & Immunology, School of Medicine, Emory University, GA, USA). She has spent most of her scientifi c careerin Dr. Compans’ lab studying virus-like particle vaccines. Currently, she is a Professor at Kyung Hee University School of Medicine, where her focusis the development of VLP protective vaccines against infl uenza and a respiratory syncytial virus (RSV). She is recognized as an expert in infl uenzaVLP vaccine research and the development of related mouse models.fquan01@gmail.comJ <strong>Vaccines</strong> Vaccin <strong>2013</strong>ISSN: 2157-7560, JVV an open access journal<strong>Vaccines</strong>-<strong>2013</strong>July 29-31, <strong>2013</strong>Volume 4 Issue 5Page 78
Leow Yee et al., J <strong>Vaccines</strong> Vaccin <strong>2013</strong>, 4:5http://dx.doi.org/10.4172/2157-7560.S1.0163 rd International Conference on<strong>Vaccines</strong> & VaccinationJuly 29-31, <strong>2013</strong> Embassy Suites Las Vegas, NV, USARNAi-based characterisation of tegument annexin as a novel vaccine candidate againtschistosomiasisLeow Yee 1,2,5 , Willis C. 1 , Loukas A. 3 , Hofmann A. 4 and Jones M. 1,21Queensland Institute of Medical Research, Australia2The University of Queensland, Australia3James Cook University, Singapore4Griffith University, Australia5Universiti Sains Malaysia, MalaysiaEfforts to develop potential vaccines against schistosomes have focused on the identification of parasite surface antigens whichcan trigger protective immunity in the host. In this study, RNA interference (RNAi) was applied to investigate the genefunction of tegument-associated annexins in S. mansoni. Expression of five annexin genes was found to be up-regulated upontransition from cercariae to schistosomula and adult worms. Silencing of annexins was facilitated by electroporation with targetspecific-dsRNAthen the isolated RNA was quantified for gene expression. Gene expression for adult parasites and schistosomulatreated with annexin-specific-dsRNA resulted in 80-96% and 87-95% reduction in transcription levels, respectively. Silencingof each annexin did not affect the parasite survival rate but conversely reduced their growth size and motility significantly atschistosomula and adult stages. Anx(Sm)3 was selected and engineered to be a recombinant chimeric peptide (rChimeric-AT) harbouring the linker region of Anx(Sm)3 and Sm-TSP-2. HLA-DR binding prediction showed that Anx(Sm)3 linker andChimeric-AT were capable to bind with 11 alleles (21.6%) and 20 alleles (49%), respectively. Sera from mice infected with S.mansoni reacted strongly with synthetic Anx(Sm)3 linker peptide and rChimeric-AT, showing that they are both immunogenic.rChimeric-AT delivered in alum induced high IgG1/IgG2a ratio, implying Th2 type response was dominant. Mice vaccinated withrChimeric-AT showed 40.4% significant reduction in intestinal egg burden as compared to the control group. Taken together, ourresults show that rChimeric-AT conferred a high level of antibody production and suggests this multi-antigen construct wouldbe a potential vaccine candidate against schistosomiasis.BiographyLeow Yee obtained his B.Sc. (Honours) and M.Sc. in Biotechnology from Universiti Sains Malaysia. Since 2006, he has been working as a Lecturerin a Malaysian government institution. In 2009, he accepted a scholarship under ASTS Fellowship from Universiti Sains Malaysia to pursue hisdoctorate degree in Vaccinology in University of Queensland under the supervision of A/Prof. Malcolm Jones. His research focus is on investigatingthe potential vaccines targeting against schistosomes. In 2011, he was awarded an Edward Jenner Ph.D. scholarship through Australian Centre forVaccine Development.yee.leow@qimr.edu.auJ <strong>Vaccines</strong> Vaccin <strong>2013</strong>ISSN: 2157-7560, JVV an open access journal<strong>Vaccines</strong>-<strong>2013</strong>July 29-31, <strong>2013</strong>Volume 4 Issue 5Page 79
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