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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
MeSH Review

Immunization, Secondary

 
 
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Disease relevance of Immunization, Secondary

 

High impact information on Immunization, Secondary

 

Chemical compound and disease context of Immunization, Secondary

 

Biological context of Immunization, Secondary

 

Anatomical context of Immunization, Secondary

  • A booster immunization also resulted in increased frequencies of IFN-gamma-secreting cells, but this increase was confined to the duodenal mucosa [18].
  • These mice showed not only a long-lasting high-titer IgM response but also a consistent high-titer IgG response (predominantly IgG1), indicating recruitment of T-cell help, although the titers of IgM and IgG antibodies following booster immunizations were not as high as they are in the response to classical T-cell-dependent antigens [19].
  • The vaginal B cell response could further be enhanced by using the Th2-type cytokines IL-4 or IL-5 as genetic adjuvants concomitantly with the DNA vaccine before intranasal booster immunization with the recombinant vaccine [20].
  • Both primary and secondary immunization with bacterial lipopolysaccharide resulted in elevation of splenic Facb-R+ lymphocytes [21].
 

Associations of Immunization, Secondary with chemical compounds

 

Gene context of Immunization, Secondary

 

Analytical, diagnostic and therapeutic context of Immunization, Secondary

  • Protection index values for challenge with either heat-labile or heat-stable toxins in ligated ileal loops were 3.4 to 4.0 in rats immunized by a parenteral primary immunization followed by two peroral booster immunizations, greater than 9 in rabbits immunized by these routes, and greater than 8 in rabbits given just three peroral immunizations [32].
  • In the first strategy, mice were primed with two biolistic intradermal inoculations with the oprF vaccine and then were given a final intramuscular booster immunization containing either a synthetic peptide-keyhole limpet hemocyanin (KLH) conjugate or a chimeric influenza virus [33].
  • Following booster immunization, mice were treated with the oral administration of 276 mg/kg/d AIF once a day for 18 days, then, the severity of CIA was evaluated by macroscopic scoring and histopathological assessment [34].

References

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  27. B7 requirements for primary and secondary protein- and polysaccharide-specific Ig isotype responses to Streptococcus pneumoniae. Wu, Z.Q., Khan, A.Q., Shen, Y., Schartman, J., Peach, R., Lees, A., Mond, J.J., Gause, W.C., Snapper, C.M. J. Immunol. (2000) [Pubmed]
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  29. Absence of functional inducible NO synthase enhances the efficacy of tolerance induced by high dose antigen feeding. Kahn, D.A., Archer, D.C., Kelly, C.J. J. Immunol. (2000) [Pubmed]
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