Skip to content
2000
Volume 13, Issue 19
  • ISSN: 1381-6128
  • E-ISSN: 1873-4286

Abstract

Malaria causes 300-500 million clinical cases and 1-3 million deaths per year, the majority of which occur in African children less than five years of age. The failure of vector control methods to achieve adequate reductions in morbidity and mortality and the widespread resistance to conventional antimalarial drugs have made development of an effective malaria vaccine a global priority. An ideal malaria vaccine should recapitulate naturally acquired immunity in an endemic setting. However, progress toward an efficacious vaccine has been slow, due to the high polymorphism of prospective target antigens and the inability of most vaccines to elicit long-lived immunological memory in the host. This review discusses the efficacy of current pre-erythrocytic-stage, asexual blood-stage, and transmission-blocking vaccine candidates, as well as future prospects for malaria vaccine development.

Loading

Article metrics loading...

/content/journals/cpd/10.2174/138161207781039805
2007-07-01
2025-04-04
Loading full text...

Full text loading...

/content/journals/cpd/10.2174/138161207781039805
Loading

  • Article Type:
    Research Article
Keyword(s): antigenic variation; innate immunity; Malaria; premunition
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test