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      Use of adenoviral vectors as veterinary vaccines

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          Abstract

          Vaccines are the most effective and inexpensive prophylactic tool in veterinary medicine. Ideally, vaccines should induce a lifelong protective immunity against the target pathogen while not causing clinical or pathological signs of diseases in the vaccinated animals. However, such ideal vaccines are rare in the veterinary field. Many vaccines are either of limited effectiveness or have harmful side effects. In addition, there are still severe diseases with no effective vaccines. A very important criterion for an ideal vaccine in veterinary medicine is low cost; this is especially important in developing countries and even more so for poultry vaccination, where vaccines must sell for a few cents a dose. Traditional approaches include inactivated vaccines, attenuated live vaccines and subunit vaccines. Recently, genetic engineering has been applied to design new, improved vaccines. Adenovirus vectors are highly efficient for gene transfer in a broad spectrum of cell types and species. Moreover, adenoviruses often induce humoral, mucosal and cellular immune responses to antigens encoded by the inserted foreign genes. Thus, adenoviruses have become a vector of choice for delivery and expression of foreign proteins for vaccination. Consequently, the market requirements for adenovirus vaccines are increasing, creating a need for production methodologies of concentrated vectors with warranted purity and efficacy. This review summarizes recent developments and approaches of adenovirus production and purification as the application of these vectors, including successes and failures in clinical applications to date.

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          Characteristics of a Human Cell Line Transformed by DNA from Human Adenovirus Type 5

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            Genetic reassortment of avian, swine, and human influenza A viruses in American pigs.

            In late summer through early winter of 1998, there were several outbreaks of respiratory disease in the swine herds of North Carolina, Texas, Minnesota, and Iowa. Four viral isolates from outbreaks in different states were analyzed genetically. Genotyping and phylogenetic analyses demonstrated that the four swine viruses had emerged through two different pathways. The North Carolina isolate is the product of genetic reassortment between H3N2 human and classic swine H1N1 influenza viruses, while the others arose from reassortment of human H3N2, classic swine H1N1, and avian viral genes. The hemagglutinin genes of the four isolates were all derived from the human H3N2 virus circulating in 1995. It remains to be determined if either of these recently emerged viruses will become established in the pigs in North America and whether they will become an economic burden.
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              Research on infectious bursal disease--the past, the present and the future.

              Infectious bursal disease (IBD) virus (IBDV) is the etiological agent of "Gumboro disease". Although first observed about 40 years ago, this disease continues to pose an important threat to the commercial poultry industry. The emergence of antigenic variant as well as very virulent strains in vaccinated flocks considerably stimulated research efforts on both, IBD and IBDV. In this review, some of the recent advances in the understanding of the structure, morphogenesis and molecular biology of the virus as well as in development of new diagnostic approaches and new strategies for vaccination against IBD are briefly summarized.
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                Author and article information

                Journal
                Gene Ther
                Gene Ther
                Gene Therapy
                Nature Publishing Group UK (London )
                0969-7128
                1476-5462
                18 October 2005
                2005
                : 12
                : Suppl 1
                : S73-S83
                Affiliations
                [1 ]Instituto de Biologia Experimental e Tecnológica/Instituto de Tecnologia Química e Biológica IBET/ITQB, Oeiras, Portugal
                [2 ]GRID grid.417993.1, ISNI 0000 0001 2260 0793, Merck and Co., Inc., ; West Point, PA USA
                [3 ]GRID grid.10772.33, ISNI 0000000121511713, Laboratório de Engenharia Bioquímica, Faculdade de Ciências e Tecnologia (FCT), Universidade Nova de Lisboa (UNL), ; Monte da Caparica, Portugal
                Article
                BF3302618
                10.1038/sj.gt.3302618
                7091679
                16231058
                4307b978-8602-46c4-a85d-72782b4d7459
                © Nature Publishing Group 2005

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

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                © Springer Nature Limited 2005

                Molecular medicine
                adenovirus vector,veterinary vaccine,viral vector production,viral vector purification

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