Current Topics in Microbiology and Immunology by G. L. Ada, P. D. Jones (auth.), A. Clarke, R. W. Compans, M.

By G. L. Ada, P. D. Jones (auth.), A. Clarke, R. W. Compans, M. Cooper, H. Eisen, W. Goebel, H. Koprowski, F. Melchers, M. Oldstone, R. Rott, P. K. Vogt, H. Wagner, I. Wilson (eds.)

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By G. L. Ada, P. D. Jones (auth.), A. Clarke, R. W. Compans, M. Cooper, H. Eisen, W. Goebel, H. Koprowski, F. Melchers, M. Oldstone, R. Rott, P. K. Vogt, H. Wagner, I. Wilson (eds.)

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The induction of a secretory antibody response to inactivated virus vaccines is dependent both on the route of administration and on the recipient's prior antigenic experience. , in nasal washes) are of low magnitude and occur infrequently after both parenteral and intranasal administration of vaccine. Parenteral administration produced a local IgG response, detected by ELISA, in 94% of primed recipients, whereas local IgA responses developed in only 38% (CLEMENTS et al. 1985). In contrast, local IgA responses develop in the majority of primed recipients after intranasal administration (WRIGHT et al.

1985). Both classes of Th cells produced IL-2, highlighting the observation (LUKACHER 1985) that class I MHC-restricted cells which were inactive as Th cells did not secrete IL-2. On this basis, it is not unreasonable to postulate that during generation in a primary (in vivo) or secondary (in vitro) response, cells of a given lineage may preferentially display different activities at different times while proliferating and differentiating after stimulation. v. injection of infectious virus - a single pulse, as only abortive replication occurs in mice.

1984). Ca recipients were completely protected against illness compared with a 72% efficacy in the inactivated virus vaccinees. Infection occurred in 19% of ca vaccinees and in 63% of inactivated virus vaccinees. Furthermore, nasal wash viral titers were 1000-fold lower in ca vaccinees shedding virus. Adult recipients of an H1N1 ca reassortant (10 7 . 8 TCID so ) were similarly protected against illness on challenge 1-3 months later (82% efficacy) and against infection - 18% of vaccinees were infected with 1000-fold lower viral titers than nonvaccinated controls (BETTS et al.

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