| Literature DB >> 17081660 |
Sandrine A L Audouy1, Saskia van Selm, Maarten L van Roosmalen, Eduard Post, Rolf Kanninga, Jolanda Neef, Silvia Estevão, Edward E S Nieuwenhuis, Peter V Adrian, Kees Leenhouts, Peter W M Hermans.
Abstract
We report the development of a novel protein-based nasal vaccine against Streptococcus pneumoniae, in which three pneumococcal proteins were displayed on the surface of a non-recombinant, killed Lactococcus lactis-derived delivery system, called Gram-positive Enhancer Matrix (GEM). The GEM particles induced the production of the proinflammatory cytokine tumour necrosis factor-alpha (TNF-alpha) by macrophages as well as the maturation of dendritic cells. The pneumococcal proteins IgA1 protease (IgA1p), putative proteinase maturation protein A (PpmA) and streptococcal lipoprotein A (SlrA) were anchored in trans to the surface of the GEM particles after recombinant production of the antigens in L. lactis as hybrids with a lactococcal cell wall binding domain, named Protein Anchor domain (PA). Intranasal immunisation with the SlrA-IgA1p or trivalent vaccine combinations without additional adjuvants showed significant protection against fatal pneumococcal pneumonia in mice. The GEM-based trivalent vaccine is a potential pneumococcal vaccine candidate that is expected to be easy to administer, safe and affordable to produce.Entities:
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Year: 2006 PMID: 17081660 DOI: 10.1016/j.vaccine.2006.09.026
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641