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Randomized Controlled Trial
. 2014 Sep;91(3):471-480.
doi: 10.4269/ajtmh.14-0119. Epub 2014 Jul 28.

Controlled human malaria infection of Tanzanians by intradermal injection of aseptic, purified, cryopreserved Plasmodium falciparum sporozoites

Randomized Controlled Trial

Controlled human malaria infection of Tanzanians by intradermal injection of aseptic, purified, cryopreserved Plasmodium falciparum sporozoites

Seif Shekalaghe et al. Am J Trop Med Hyg. 2014 Sep.

Abstract

Controlled human malaria infection (CHMI) by mosquito bite has been used to assess anti-malaria interventions in > 1,500 volunteers since development of methods for infecting mosquitoes by feeding on Plasmodium falciparum (Pf) gametocyte cultures. Such CHMIs have never been used in Africa. Aseptic, purified, cryopreserved Pf sporozoites, PfSPZ Challenge, were used to infect Dutch volunteers by intradermal injection. We conducted a double-blind, placebo-controlled trial to assess safety and infectivity of PfSPZ Challenge in adult male Tanzanians. Volunteers were injected intradermally with 10,000 (N = 12) or 25,000 (N = 12) PfSPZ or normal saline (N = 6). PfSPZ Challenge was well tolerated and safe. Eleven of 12 and 10 of 11 subjects, who received 10,000 and 25,000 PfSPZ respectively, developed parasitemia. In 10,000 versus 25,000 PfSPZ groups geometric mean days from injection to Pf positivity by thick blood film was 15.4 versus 13.5 (P = 0.023). Alpha-thalassemia heterozygosity had no apparent effect on infectivity. PfSPZ Challenge was safe, well tolerated, and infectious.

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Conflict of interest statement

Disclosure: Sanaria Inc. manufactured PfSPZ Challenge, and Protein Potential LLC is affiliated with Sanaria. Thus, all authors associated with Sanaria or Protein Potential have potential conflicts of interest. There are no other conflicts of interest.

Figures

Figure 1.
Figure 1.
Flow chart of recruitment and study design.
Figure 2.
Figure 2.
Parasite density as measured by qPCR in the 10,000 (A) and 25,000 (B) PfSPZ dose groups. Panels A (N = 11) and B (N = 10) show individual and geometric mean parasite density (parasites/mL) of positive volunteers from day of inoculation through last day of positivity after initiation of treatment. Panel C shows an overlay of geometric mean parasite densities with confidence intervals (95%) of positive volunteers in each group (Black line = Group 1, 10,000 PfSPZ; Grey line = Group 2, 25,000 PfSPZ).* *For Panel B, the geometric mean was calculated excluding the single volunteer who first became positive on Day 16.

Comment in

References

    1. Mayne B. The injection of mosquito sporozoites in malaria therapy. Public Health Rep. 1933;48:909–913.
    1. Mayne B, Young M. The technique of induced malaria as used in the South Carolina State Hospital. J Vener Dis Inf. 1941;22:271–276.
    1. Boyd MF. Malariology: A Comprehensive Survey of All Aspects of This Group of Diseases from a Global Standpoint. Philadelphia, PA: W. B. Saunders; 1949.
    1. Ifediba T, Vanderberg JP. Complete in vitro maturation of Plasmodium falciparum gametocytes. Nature. 1981;294:364–366. - PubMed
    1. Campbell CC, Collins WE, Nguyen Dinh P, Barber A, Broderson JR. Plasmodium falciparum gametocytes from culture in vitro develop to sporozoites that are infectious to primates. Science. 1982;217:1048–1050. - PubMed

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