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Chapter category: Vaccines

Recombinant Live Attenuated Viral Vaccines

This chapter appears in the following book:

New Vaccine Technologies

Edited by: Ronald W. Ellis
ISBN: 1-58706-050-7
» Get more information about this book at landesbioscience.com «

Chapter authors:
Richard R. Spaete

Vaccination with live attenuated viruses in general offers a number of advantages as a strategy to evoke an effective and long lasting immune response. Foremost among these is the possibility of a nearly complete presentation of the antigenic repertoire of the pathogen to the immune system. Both structural and non-structural antigens are available to stimulate humoral and cell-mediated immune responses in association with either class I or class II HLA molecules. Antigenic structures will be appropriately presented in authentic states of conformation and oligomerization. Taking advantage of the infectious nature of the virus obviates the need for an adjuvant/antigen delivery system. Obviously, the ability of the vaccine virus to amplify will also increase the antigenic dose and influence the magnitude of the immune response. The ability to amplify depends on the state of attenuation or the nature of the block to replication (as with DISC viruses discussed below).

Delivery of vaccines via the pathogen's natural portal of entry including mucosal and oral routes, will be increasingly used in the future. By mimicking the route or portal of infection, this mode of administration: 1) stimulates immunity at the portal of entry, and 2) stimulates multiple components of the immune system. Intranasal administration offers the possibility of achieving protection of the upper and lower respiratory tract. Intranasal delivery can also stimulate immunity in the urogenital tract. In common with vaccine delivery by parenteral routes, these vaccines also present multiple protective antigens in their native conformation. Another attractive feature of this mode of delivery is that needles are not necessary for administration. This feature is especially popular in pediatric populations!

In comparison with other vaccine approaches, live vaccines also have the advantage of relatively low cost of manufacture. The ability of the vaccines to replicate is the primary reason for this advantage. In many instances, one eucaryotic cell can yield several doses of vaccine. Costs associated with product characterization and general safety testing are common to any vaccine approach and live vaccines do not a priori incur any additional cost burden. Necessarily, the nature of the tests will be unique to the product depending on whether the vaccine is a subunit, a killed virus or a polynucleotide vaccine. In some cases, the benefit to the consumer may be economic as well as improved compliance resulting from the need for fewer doses with live attenuated vaccines.

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