| Literature DB >> 16779733 |
Brad J Spellberg1, Ashraf S Ibrahim, Valentina Avanesian, Yue Fu, Carter Myers, Quynh T Phan, Scott G Filler, Michael R Yeaman, John E Edwards.
Abstract
We have shown that vaccination with the recombinant N terminus of Als1p (rAls1p-N) protects mice against disseminated and oropharyngeal candidiasis. We now report that vaccination of mice with a related candidate, rAls3p-N, induces a broader antibody response than rAls1p-N and a similar cell-mediated immune response. The rAls3p-N vaccine was equally as effective as rAls1p-N against disseminated candidiasis but was more effective than rAls1p-N against oropharyngeal or vaginal candidiasis. Antibody titers did not correlate with protection against disseminated candidiasis, but delayed-type hypersensitivity did. The rAls3p-N vaccine is a promising new vaccine candidate for further exploration to prevent systemic and mucosal candidal infections.Entities:
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Year: 2006 PMID: 16779733 DOI: 10.1086/504691
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226