1984
DOI: 10.1111/j.1398-9995.1984.tb01949.x
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Relevance of Animal Models for Studies of Immune Regulation of Atopic Allergy

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Cited by 16 publications
(7 citation statements)
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“…For the study on allergic diseases, several experimental models showing type I reaction or eosinophilic inflammation have been developed in mice, rats, and guinea pigs by using Ascaris, ovalbumin, and other allergens [20]. In addition, several studies showed that active immunization of monkeys with pollen allergens including recombinant Bet v 1 and Bet v 2 induced antigen-specific IgE production and some allergic symptoms [8,9].…”
Section: Discussionmentioning
confidence: 99%
“…For the study on allergic diseases, several experimental models showing type I reaction or eosinophilic inflammation have been developed in mice, rats, and guinea pigs by using Ascaris, ovalbumin, and other allergens [20]. In addition, several studies showed that active immunization of monkeys with pollen allergens including recombinant Bet v 1 and Bet v 2 induced antigen-specific IgE production and some allergic symptoms [8,9].…”
Section: Discussionmentioning
confidence: 99%
“…IgE antibodies, mast cells, basophils, eosinophils, neutrophils, macro phages and mucous cells, appear in asthmatic disor ders and their release of mediators seems to result in clinically manifested allergic inflammation and hy perreactivity [1]. The relative contribution of the var ious cells and their mediators in the disease has not been settled, however.…”
Section: Introductionmentioning
confidence: 99%
“…In rodents it is possible to raise a humoral immune response restricted to distinct immunoglobulin classes by means of different adjuvants. Extracts of Ascaris, Nippostrongylus brasiliensis or Bordetella pertussis and lipopolysaccharide, alum or aluminiumhydroxide will potentiate an IgE-response, while Freund's complete adjuvant will principally induce IgG and suppress the IgE-response (5,105). In humans, IgE is similarly potentiated by extracts of bacteria and parasites mentioned above (5), whereas alum-and Al(OH)3-adsorbed allergen in two controlled immunotherapy studies have demonstrated clinical effects comparable to aqueous extracts (66,79).…”
Section: Mixture Emulgation or Adsorptionmentioning
confidence: 99%
“…Extracts of Ascaris, Nippostrongylus brasiliensis or Bordetella pertussis and lipopolysaccharide, alum or aluminiumhydroxide will potentiate an IgE-response, while Freund's complete adjuvant will principally induce IgG and suppress the IgE-response (5,105). In humans, IgE is similarly potentiated by extracts of bacteria and parasites mentioned above (5), whereas alum-and Al(OH)3-adsorbed allergen in two controlled immunotherapy studies have demonstrated clinical effects comparable to aqueous extracts (66,79). Compared with aque-ous allergen extract no higher levels of specific IgE were observed (66), w^hereas the levels of specific IgG were slightly increased (66) or unchanged (79).…”
Section: Mixture Emulgation or Adsorptionmentioning
confidence: 99%