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Chapter 15 : Immunization against Viral Diseases

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Abstract:

This chapter provides a review of the current viral vaccine practices and concepts, and indicates future directions for vaccine research and development. ‘‘Active immunization’’ to a virus can be induced through natural infection or by vaccination. ‘‘Passive immunization’’ refers to a transfer of temporary immunity to the host, and provides transient immune-mediated protection from infection or disease. Immunization can influence antibody-mediated immunity in many ways. First, by increasing the repertoire and the frequency of immunoglobulin receptors on memory B cells capable of recognizing a particular antigen, the kinetics of antibody production on subsequent exposure will be more rapid. Second, somatic hypermutation and B-cell selection result in antibodies of successively higher affinities, so repeated virus infection or immunization will cause affinity maturation. Third, immunization with a vaccine formulation that promotes IFN-γ production will increase the production of the immunoglobulin G1 (IgG1) and IgG3 subclasses. Finally, repeated immunization can improve the breadth of antibody responses to a particular virus by recruiting new responses to different antigenic regions. Many killed or inactivated and subunit viral vaccines have also been licensed for the prevention of viral diseases. The major advantage of inactivated vaccines is that there is no risk of infection in the vaccinated patient or of transmission of live virus to potentially immunocompromised close contacts of vaccinees. In general, the most effective way of protecting people with immunodeficiencies from vaccine-preventable diseases is to make sure the people around them are well vaccinated and are not transmitters of infection.

Citation: Martin J, Graham B. 2009. Immunization against Viral Diseases, p 333-349. In Richman D, Whitley R, Hayden F (ed), Clinical Virology, Third Edition. ASM Press, Washington, DC. doi: 10.1128/9781555815981.ch15

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FIGURE 1

Recognition of viral pathogens. Eukaryotes have evolved mechanisms to detect potential microbial pathogens as they encounter the plasma membrane or penetrate the endosomal or cytoplasmic compartment of the cell. The molecules that interact with microbe-derived ligands trigger signaling pathways that lead to inflammatory responses. Harnessing the coordinated regulation of immune responses elicited by TLRs and helicases is a major focus of new adjuvant development for vaccines.

Citation: Martin J, Graham B. 2009. Immunization against Viral Diseases, p 333-349. In Richman D, Whitley R, Hayden F (ed), Clinical Virology, Third Edition. ASM Press, Washington, DC. doi: 10.1128/9781555815981.ch15
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Tables

Generic image for table
TABLE 1

Impact of licensed vaccines on annual prevalence of selected viral diseases reported in the United States

Citation: Martin J, Graham B. 2009. Immunization against Viral Diseases, p 333-349. In Richman D, Whitley R, Hayden F (ed), Clinical Virology, Third Edition. ASM Press, Washington, DC. doi: 10.1128/9781555815981.ch15
Generic image for table
TABLE 2

Vaccines licensed for use in the United States against viral diseases

Citation: Martin J, Graham B. 2009. Immunization against Viral Diseases, p 333-349. In Richman D, Whitley R, Hayden F (ed), Clinical Virology, Third Edition. ASM Press, Washington, DC. doi: 10.1128/9781555815981.ch15
Generic image for table
TABLE 3

Characteristics of vaccine approaches used to prevent viral diseases

Citation: Martin J, Graham B. 2009. Immunization against Viral Diseases, p 333-349. In Richman D, Whitley R, Hayden F (ed), Clinical Virology, Third Edition. ASM Press, Washington, DC. doi: 10.1128/9781555815981.ch15

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