From experimental models and the analyses of patients, it is well documented that antigen-specific T cells are critical for protection against Leishmania infection. Effective vaccines require both targeting to the pathogen and an immune stimulant to induce maturation of appropriate immune responses. While a great number of antigens have been examined as vaccine candidates against various Leishmania species, few have advanced to human or canine clinical trials. With emphasis on antigen expression, in this minireview we discuss some of the vaccine platforms that are currently being explored for the development of Leishmania vaccines. It is clear that the vaccine platform of choice can have a significant impact upon the level of protection induced by particular antigens, and we provide and highlight some examples for which the vaccine system used has impacted the protective efficacy imparted.
Keyphrases
- clinical trial
- immune response
- dendritic cells
- end stage renal disease
- endothelial cells
- poor prognosis
- ejection fraction
- newly diagnosed
- chronic kidney disease
- attention deficit hyperactivity disorder
- randomized controlled trial
- study protocol
- toll like receptor
- open label
- high throughput
- inflammatory response
- single cell
- patient reported outcomes