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Inactivated pep27 mutant as an effective mucosal vaccine against a secondary lethal pneumococcal challenge in mice
Clinical and Experimental Vaccine Research ; : 58-65, 2013.
Article Dans Anglais | WPRIM | ID: wpr-195042
ABSTRACT

PURPOSE:

A pep27 mutant may be able to elicit mucosal immunity against pneumococcal diseases, and could be employed as an inexpensive attenuated vaccine. However, this particular mutant contains an erythromycin-resistance marker. The purpose of the current study is to develop a markerless pep27 mutant and assess whether this inactivated mutant is able to induce mucosal immunity. MATERIALS AND

METHODS:

Mice were vaccinated intranasally with the inactivated markerless pep27 mutant every 2 weeks for a total of three times, after which time serum samples were analyzed for antibody titers. The mice were then challenged with a lethal D39 strain and their survival time was measured. The cross-reactivity of the antisera against pep27 was also compared to other mutant serotypes.

RESULTS:

Intranasal immunization of mice with the inactivated markerless pep27 mutant provides effective protection and rapidly cleared bacterial colonization in vivo. Moreover, antisera raised against the pep27 mutant may cross-react with several other serotype strains.

CONCLUSION:

Intranasal immunization with the inactivated pep27 mutant may be able to provide mucosal immunity, and could represent an efficient mucosal vaccine.
Sujets)

Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Entorses et foulures / Streptococcus pneumoniae / Immunisation / Côlon / Immunité muqueuse / Sérums immuns Limites du sujet: Animaux langue: Anglais Texte intégral: Clinical and Experimental Vaccine Research Année: 2013 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Entorses et foulures / Streptococcus pneumoniae / Immunisation / Côlon / Immunité muqueuse / Sérums immuns Limites du sujet: Animaux langue: Anglais Texte intégral: Clinical and Experimental Vaccine Research Année: 2013 Type: Article