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Experimental infection and protection against ... - TI Pharma

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Introduction 21<br />

- to identify parameters influencing the power of CHMI to detect vaccine<br />

efficacy of pre-erythrocytic <strong>and</strong> erythrocytic malaria vaccines (Chapter<br />

6)<br />

We next will address two important aspects of improvement to the CHMI model:<br />

- to increase the portfolio of Pf strains that can be used for <strong>infection</strong><br />

(Chapter 7)<br />

- to investigate the administration of parasites by needle (Chapter 8)<br />

Can <strong>protection</strong> to malaria in humans be efficiently induced by inoculation of<br />

live whole sporozoites?<br />

The inoculation of irradiated sporozoites by mosquito bite has shown to induce<br />

full <strong>protection</strong> in humans, albeit inefficiently <strong>and</strong> with limited longevity. We will<br />

explore whether viable intact sporozoites induce <strong>protection</strong> more efficiently,<br />

eventually aiming to create a model for malaria immunity. The administration of<br />

chloroquine prophylaxis will prevent clinical disease whilst the exposure to<br />

viable sporozoites allows exposure of parasite antigen. We address the following<br />

specific objectives:<br />

- to induce <strong>protection</strong> to Pf malaria in malaria naïve volunteers by<br />

exposure to parasites whilst taking chloroquine prophylaxis (Chapter 9)<br />

- to investigate the longevity of induced <strong>protection</strong> (Chapter 10)

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