Malaria Vaccines: AMA1-rEPA/ALHYDROGEL + CPG 7909
Malaria Vaccines: AMA1-rEPA/ALHYDROGEL + CPG 7909
批准号:
7592357
负责人:
Laura Martin
金额:
$122.83万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
AffectAfricanAlhydrogelAllelesAntibodiesAntibody FormationAntigensAreaBloodCarrier ProteinsCessation of lifeChildClinical TrialsCollaborationsComplement component C1sConjugate VaccinesCouplingDiseaseEffectivenessErythrocytesGoalsGrowthHumanImmuneImmune responseImmune systemImmunologic MemoryIncidenceIndividualInfantInfectionMalariaMalaria VaccinesMethodsNational Institute of Allergy and Infectious DiseaseNatural ImmunityNumbersParasitesPhaseProteinsPseudomonas aeruginosa toxA proteinRecombinantsResearchSeveritiesStagingStreamT-LymphocyteVaccinationVaccinesWorkasexualblood leadimmunogenicimmunogenicityimprovedpressurepreventprototyperesponsetransmission processvaccine developmentvolunteer
中文摘要
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英文摘要
Malaria Vaccine Development Branch (MVDB) General Description: The Malaria Vaccine Development Branch (MVDB) is an NIAID initiative working in close collaboration with DMID to respond to the global need for vaccines against malaria. The Malaria Vaccine Development Branch (MVDB) was commissioned in 2001 to research, develop, and produce prototype malaria vaccines and conduct early-phase clinical trials of promising vaccine candidates. Our overarching goal is to develop malaria vaccines that will reduce severe disease and death among African children and eliminate malaria from low-transmission areas of the world.
An asexual blood-stage vaccine will elicit immune responses capable of either destroying malaria parasites in the blood stream or inhibiting parasites from infecting red blood cells. In either case, the net effect is to reduce or prevent burden of parasites and hence decrease the incidence, severity, or the complications of disease. Such a vaccine would target blood-stage parasite proteins since these antigens are abundantly expressed by parasites during persistent infections. It would act to prime the immune system for subsequent infection in infants or it would boost already present, yet weak, natural immunity in young children. Furthermore, a vaccine composed of multiple antigens will increase the number of individuals responding to at least one component of the vaccine. The inclusion of multiple alleles of polymorphic proteins would also minimize immune pressure on parasite selection, thus decreasing the likelihood of parasite breakthrough.
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