Publication | Closed Access
A synthetic malaria vaccine elicits a potent CD8+ and CD4+ T lymphocyte immune response in humans. Implications for vaccination strategies
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Citations
33
References
2001
Year
Adaptive Immune SystemImmunologyImmune RegulationImmunodominanceAntigen ProcessingCd4 T Cell ResponsesInnate ImmunityImmunotherapeuticsPlasmodium FalciparumImmune SystemSynthetic ImmunologyCd4+ TSynthetic Malaria VaccineVaccination StrategiesTherapeutic VaccineT Cell ImmunityHumoral ImmunitySystems ImmunologyVaccinationStrong Cd8+Vaccine DesignMedicineVaccine ResearchViral Immunity
We report the first synthetic peptide vaccine eliciting strong CD8+ and CD4+ T lymphocyte responses in humans. The vaccine, representing the C-terminal region of the circumsporozoite protein of Plasmodium falciparum (amino acids 282–383) was well tolerated and strong sporozoite-specific antibodies were elicited. In addition, robust lymphocyte proliferation responses were equally elicited with concomitant in vitro production of IFN-γ, crucial in the elimination of the parasite. Most importantly, we also observed the development of CD8+ T lymphocyte responses decisive in the immunity to malaria. The latter finding opens new, possibly safer, avenues for vaccination strategies when a CD8+ T cell response is needed.
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