Author:
Mathias-Santos Camila,Rodrigues Juliana F.,Sbrogio-Almeida Maria Elisabete,Connell Terry D.,Ferreira Luís C. S.
Abstract
ABSTRACTThe type I and type II heat-labile enterotoxins (LT-I and LT-II) are strong mucosal adjuvants when they are coadministered with soluble antigens. Nonetheless, data on the parenteral adjuvant activities of LT-II are still limited. Particularly, no previous study has evaluated the adjuvant effects and induced inflammatory reactions of LT-II holotoxins or their B pentameric subunits after delivery via the intradermal (i.d.) route to mice. In the present report, the adjuvant and local skin inflammatory effects of LT-IIa and its B subunit pentamer (LT-IIaB5) were determined. When coadministered with ovalbumin (OVA), LT-IIa and, to a lesser extent, LT-IIaB5exhibited serum IgG adjuvant effects. In addition, LT-IIa but not LT-IIaB5induced T cell-specific anti-OVA responses, particularly in respect to induction of antigen-specific cytotoxic CD8+T cell responses. LT-IIa and LT-IIaB5induced differential tissue permeability and local inflammatory reactions after i.d. injection. Of particular interest was the reduced or complete lack of local reactions, such as edema and tissue induration, in mice i.d. inoculated with LT-IIa and LT-IIaB5,respectively, compared with mice immunized with LT-I. In conclusion, the present results show that LT-IIa and, to a lesser extent, LT-IIaB5exert adjuvant effects when they are delivered via the i.d. route. In addition, the low inflammatory effects of LT-IIa and LT-IIaB5in comparison to those of LT-I support the usefulness of LT-IIa and LT-IIaB5as parenterally delivered vaccine adjuvants.
Publisher
American Society for Microbiology
Subject
Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy
Cited by
11 articles.
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