Pharmaceutical compositions and methods to vaccinate against candidiasis
A Candida albicans bloodstream infections cause significant morbidity and mortality in hospitalized patients. Filament formation and adherence to host cells are critical virulence factors of C. albicans . Multiple filamentation regulatory pathways have been discovered, however the downstream effectors of these regulatory pathways remain unknown. The cell surface proteins in the ALS group are downstream effectors of the filamentation regulatory pathway. Particularly, Als1p mediates adherence to endothelial cells in vitro and is required for virulence. The blocking of adherence by the organism is described resulting from the use of a composition and method disclosed herein. Specifically, a pharmaceutical composition comprised of a gene, gene product, or specific antibody to the ALS gene family is administered as a vaccine to generate an immune response capable of blocking adherence of the organism.
1. A method of vaccinating a mammalian host against Candida albicans comprising administering to said host a pharmacologically effective amount of a vaccine comprising an isolated polypeptide consisting of the N-terminal domain of the Candida albicans agglutinin like sequence (ALS) polypeptide, Als1p, in a pharmaceutically acceptable excipient, wherein the N-terminal domain extends from the end of the signal peptide to the beginning of the tandem repeat of said Candida albicans Als1p, and wherein the method inhibits adhesion of the Candida albicans to endothelial cells in said host.
2. The method of claim 1 , wherein the immunogenic composition is administered subcutaneously.
3. The method of claim 1 , wherein the polypeptide is substantially pure.
4. The method of claim 1 , wherein the composition comprises an immunostimulating adjuvant.
5. The method of claim 3 , wherein the immunostimulating adjuvant is alum.
6. The method of any one of claims 1 to 5 , wherein said administering comprises administering a booster dose of the immunogenic composition.
7. The method of claim 1 , wherein the polypeptide is produced in Saccharomyces cerevisiae.
8. The method of claim 1 , wherein the mammalian host is a human and said polypeptide is purified.
9. The method of claim 1 wherein the polypeptide consists of amino acids 18 to 432 of the amino acid sequence of SEQ ID NO: 25.