Abstract
Mucosal delivery of vaccines against sexually transmitted pathogens is important to elicit strong immune responses at biologically relevant sites. However, inclusion of appropriate adjuvants is essential to overcome the inherent mucosal tolerance. We present evidence in support of the effectiveness of co-administering alpha-galactosylceramide (α-GalCer) as an adjuvant with a CTL-inducing HIV envelope peptide, via either oral or intranasal route, to prime antigen-specific immune responses in multiple systemic and mucosal compartments. Contrary to the known potential of repeated parenteral dosing with α-GalCer to induce NKT cell anergy that could compromise adoptive immunity development, we have observed that two and three doses delivered by the intranasal or oral route were more efficient in priming broader antigen-specific immune responses. These results demonstrate the effectiveness of α-GalCer as adjuvant for repeated intranasal or oral administration of vaccines for protection against mucosally transmitted pathogens.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 3335-3341 |
| Number of pages | 7 |
| Journal | Vaccine |
| Volume | 27 |
| Issue number | 25-26 |
| DOIs | |
| State | Published - May 26 2009 |
Keywords
- Cellular immunity
- Mucosal immunization
- α-Galactosylceramide
ASJC Scopus subject areas
- Molecular Medicine
- General Immunology and Microbiology
- General Veterinary
- Public Health, Environmental and Occupational Health
- Infectious Diseases
MD Anderson CCSG core facilities
- Flow Cytometry and Cellular Imaging Facility
- Research Animal Support Facility
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