Plasmodium vivax sporozoite challenge in malaria-naïve and semi-immune Colombian volunteers

Myriam Arévalo-Herrera, David A Forero-Peña, Kelly Rubiano, José Gómez-Hincapie, Nora L Martínez, Mary Lopez-Perez, Angélica Castellanos, Nora Céspedes, Ricardo Palacios, José Millán Oñate, Sócrates Herrera, Myriam Arévalo-Herrera, David A Forero-Peña, Kelly Rubiano, José Gómez-Hincapie, Nora L Martínez, Mary Lopez-Perez, Angélica Castellanos, Nora Céspedes, Ricardo Palacios, José Millán Oñate, Sócrates Herrera

Abstract

Background: Significant progress has been recently achieved in the development of Plasmodium vivax challenge infections in humans, which are essential for vaccine and drug testing. With the goal of accelerating clinical development of malaria vaccines, the outcome of infections experimentally induced in naïve and semi-immune volunteers by infected mosquito bites was compared.

Methods: Seven malaria-naïve and nine semi-immune Colombian adults (n = 16) were subjected to the bites of 2-4 P. vivax sporozoite-infected Anopheles mosquitoes. Parasitemia levels, malaria clinical manifestations, and immune responses were assessed and compared.

Results: All volunteers developed infections as confirmed by microscopy and RT-qPCR. No significant difference in the pre-patent period (mean 12.5 and 12.8 days for malaria-naïve and malaria-exposed, respectively) was observed but naïve volunteers developed classical malaria signs and symptoms, while semi-immune volunteers displayed minor or no symptoms at the day of diagnosis. A malaria-naïve volunteer developed a transient low submicroscopic parasitemia that cured spontaneously. Infection induced an increase in specific antibody levels in both groups.

Conclusion: Sporozoite infectious challenge was safe and reproducible in semi-immune and naïve volunteers. This model will provide information for simultaneous comparison of the protective efficacy of P. vivax vaccines in naïve and semi-immune volunteers under controlled conditions and would accelerate P. vivax vaccine development.

Trial registration: clinicaltrials.gov NCT01585077.

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1. Flow chart of study design…
Figure 1. Flow chart of study design and volunteers recruitment.
Figure 2. Course of parasitemia determined by…
Figure 2. Course of parasitemia determined by RT-qPCR.
Parasitemia determined between days 0 and 16 of post-challenge follow-up. Each point represents parasites/µL (Log10) in (A) naïve (n = 6) and (B) semi-immune (n = 9) volunteers. Solid lines represent pretreatment and dashed lines post-treatment.
Figure 3. Specific antibody responses against P.…
Figure 3. Specific antibody responses against P. vivax antigens in naïve and semi-immune volunteers.
Antibodies are expressed as reactivity index defined as OD values of tested sample divided by the cut-off value. Reactivity indexes against (A) PvsCs and (B) PvMSP-1 in naïve volunteers (n = 7). Reactivity indexes against (C) PvsCS and (D) PvMSP-1 in semi-immune volunteers (n = 9).

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Source: PubMed

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