Search Results - "de Vogel, C. P"
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Immune evasion cluster-positive bacteriophages are highly prevalent among human Staphylococcus aureus strains, but they are not essential in the first stages of nasal colonization
Published in Clinical microbiology and infection (01-03-2011)“…The Staphylococcus aureus immune evasion cluster (IEC), located on β-haemolysin-converting bacteriophages (βC-Φs), encodes the immune-modulating proteins…”
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Induction of antibodies by Staphylococcus aureus nasal colonization in young children
Published in Clinical microbiology and infection (01-08-2010)“…In order to develop novel antlstaphylococcal strategies, understanding the determinants of carriage and how humans respond to Staphylococcus aureus exposure is…”
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Streptococcus pneumoniae exposure is associated with human metapneumovirus seroconversion and increased susceptibility to in vitro HMPV infection
Published in Clinical microbiology and infection (01-12-2011)“…It remains largely unknown which factors determine the clinical outcome of human metapneumovirus (HMPV) infections. The aim of the present study was to analyse…”
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Heterogeneity of the humoral immune response following Staphylococcus aureus bacteremia
Published in European journal of clinical microbiology & infectious diseases (01-05-2010)“…Expanding knowledge on the humoral immune response in Staphylococcus aureus-infected patients is a mandatory step in the development of vaccines and…”
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Development of a multiplexed bead-based immunoassay for the simultaneous detection of antibodies to 17 pneumococcal proteins
Published in European journal of clinical microbiology & infectious diseases (01-04-2011)“…Presently, several pneumococcal proteins are being evaluated as potential vaccine candidates. Here, we gather novel insights in the immunogenicity of PLY,…”
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Immunogenicity of Toxins during Staphylococcus aureus Infection
Published in Clinical infectious diseases (01-01-2010)“…Background Toxins are important Staphylococcus aureus virulence factors, but little is known about their immunogenicity during infection. Here, additional…”
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