4.5 Article

Cross-stage immunity for malaria vaccine development

期刊

VACCINE
卷 33, 期 52, 页码 7513-7517

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.vaccine.2015.09.098

关键词

Malaria; Vaccine; Immunization; Cross-stage; Pre-erythrocytic; Blood-stage

资金

  1. Medical Research Council [U117584248]
  2. EviMalaR PhD fellowship (European Union) [242095-EVIMalaR]
  3. Bill and Melinda Gates Foundation [OPP1080385, OPP1091355]
  4. Bill and Melinda Gates Foundation [OPP1091355, OPP1080385] Funding Source: Bill and Melinda Gates Foundation
  5. MRC [MC_U117584248] Funding Source: UKRI
  6. Medical Research Council [MC_U117584248] Funding Source: researchfish
  7. The Francis Crick Institute [10101] Funding Source: researchfish

向作者/读者索取更多资源

A vaccine against malaria is urgently needed for control and eventual eradication. Different approaches are pursued to induce either sterile immunity directed against pre-erythrocytic parasites or to mimic naturally acquired immunity by controlling blood-stage parasite densities and disease severity. Pre-erythrocytic and blood-stage malaria vaccines are often seen as opposing tactics, but it is likely that they have to be combined into a multi-stage malaria vaccine to be optimally safe and effective. Since many antigenic targets are shared between liver- and blood-stage parasites, malaria vaccines have the potential to elicit cross-stage protection with immune mechanisms against both stages complementing and enhancing each other. Here we discuss evidence from pre-erythrocytic and blood-stage subunit and whole parasite vaccination approaches that show that protection against malaria is not necessarily stage-specific. Parasites arresting at late liver-stages especially, can induce powerful blood-stage immunity, and similarly exposure to blood-stage parasites can afford pre-erythrocytic immunity. The incorporation of a blood-stage component into a multi-stage malaria vaccine would hence not only combat breakthrough infections in the blood should the pre-erythrocytic component fail to induce sterile protection, but would also actively enhance the pre-erythrocytic potency of this vaccine. We therefore advocate that future studies should concentrate on the identification of cross-stage protective malaria antigens, which can empower multi-stage malaria vaccine development. (C) 2015 The Authors. Published by Elsevier Ltd.

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