An effective vaccine delivery system has been developed for vaccinatio
n against a blood-stage malaria infection in mice. Subcutaneous vaccin
ation with a semi-purified asexual blood-stage malaria antigen combine
d with an adjuvant formulation containing squalane, Tween 80 and pluro
nic L121 (AF) protected mice infected with a lethal P. yoelii infectio
n against death and greatly reduced the severity and duration of paras
itaemia. The adjuvant and the route of immunization are both clinicall
y acceptable, thereby making this an attractive delivery system for a
human malaria vaccine. Protective immunity appeared to be associated w
ith an enhancement of both Th1 and Th2 subset cytokines.