Affiliation:
1. Institute of Oral Biology, Faculty of Dentistry, University of Oslo, Oslo, Norway
Abstract
Streptococcus pneumoniae
causes various diseases worldwide. Current pneumococcal vaccines protect against a limited number of more than 90 pneumococcal serotypes, accentuating the urgent need to develop novel prophylactic strategies.
S. pneumoniae
and the commensal
Streptococcus mitis
share immunogenic characteristics that make
S. mitis
an attractive vaccine candidate against
S. pneumoniae
. In this study, we evaluated the potential of
S. mitis
and its mutant expressing pneumococcal capsule type 4 (
S. mitis
TIGR4cps) to induce protection against
S. pneumoniae
lung infection in mice. Our findings show that intranasal vaccination with
S. mitis
protects against
S. pneumoniae
strains D39 (serotype 2) and TIGR4 (serotype 4) in a serotype-independent fashion, which is associated with enhanced antibody and T cell responses. Furthermore,
S. mitis
TIGR4cps conferred additional protection against
S. pneumoniae
TIGR4, but not against D39. The findings highlight the potential of
S. mitis
to generate protection that combines both serotype-independent and serotype-specific responses.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
21 articles.
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