Page 798 - Veterinary Immunology, 10th Edition
P. 798

BCG                    Macrophage stimulator
  VetBooks.ir                   Bordetella pertussis   Lymphocyte stimulator
                                Muramyl dipeptide
                                                       Macrophage stimulator
                                Lipopolysaccharide
                                                       Macrophage stimulator
                Immune stimulators Saponin
                                                       Stimulates antigen processing
                                Lysolecithin           Stimulates antigen processing
                                Pluronic detergents    Stimulates antigen processing
                                Glucans                Macrophage stimulator
                                Dextran sulfate        Macrophage stimulator
                Delivery systems  Liposomes            Stimulates antigen processing
                                ISCOMs                 Stimulates antigen processing
                                Microparticles         Stimulates antigen processing
                Mixed adjuvants  Freund's complete adjuvant  Depot plus immune stimulant
               BCG, Bacillus Calmette-Guérin; DAMPs, damage-associated molecular patterns; ISCOMs,
               immune-stimulating complexes.



               Aluminum Salts


               These have been used since the 1920s and they are by far the most
               widely employed adjuvants. They come in different forms
               including aluminum hydroxide gel (which is actually aluminum

               oxyhydroxide), aluminum phosphate gel,
               hydroxysulphophosphate, and aluminum potassium sulfate (alum),
               as well as calcium phosphate These salts have different physical

               characteristics and adjuvant properties.
                  For many years aluminum salts were added to veterinary
               vaccines in the belief that they formed a depot in the tissues from
               which antigens slowly leak and thus give a prolonged strong
               immune response. It is now recognized that a depot effect is not

               required for their adjuvant effect. Aluminum-adjuvanted vaccines
               induce inflammatory nodules at the injection site. These contain
               neutrophils with some eosinophils and lymphocytes in the first 48

               hours. Recruitment of mature myeloid dendritic cells to the sites of
               injection is enhanced. Likewise, activated macrophages are
               attracted to these sites and these macrophages may develop into
               dendritic cells.
                  Removal of the injection site nodule and its associated alum

               depot as early as 2 hours after vaccination has no significant effect
               on either T or B immune responses to the vaccine. Alum appears to
               affect lipids in the plasma membrane and promotes dendritic cell

               (DC) homing to lymph nodes. Additionally, alum kills
               inflammatory cells such as neutrophils resulting in DNA release
               and enhancing DC–T cell interactions. (Fig. 24.11). Although alum
               has been the most widely used adjuvant in veterinary vaccines, its




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