[HTML][HTML] Optimising Controlled Human Malaria Infection Studies Using Cryopreserved P. falciparum Parasites Administered by Needle and Syringe
SH Sheehy, AJ Spencer, AD Douglas, BKL Sim… - PloS one, 2013 - journals.plos.org
PloS one, 2013•journals.plos.org
Background Controlled human malaria infection (CHMI) studies have become a routine tool
to evaluate efficacy of candidate anti-malarial drugs and vaccines. To date, CHMI trials have
mostly been conducted using the bite of infected mosquitoes, restricting the number of trial
sites that can perform CHMI studies. Aseptic, cryopreserved P. falciparum sporozoites
(PfSPZ Challenge) provide a potentially more accurate, reproducible and practical
alternative, allowing a known number of sporozoites to be administered simply by injection …
to evaluate efficacy of candidate anti-malarial drugs and vaccines. To date, CHMI trials have
mostly been conducted using the bite of infected mosquitoes, restricting the number of trial
sites that can perform CHMI studies. Aseptic, cryopreserved P. falciparum sporozoites
(PfSPZ Challenge) provide a potentially more accurate, reproducible and practical
alternative, allowing a known number of sporozoites to be administered simply by injection …
Background
Controlled human malaria infection (CHMI) studies have become a routine tool to evaluate efficacy of candidate anti-malarial drugs and vaccines. To date, CHMI trials have mostly been conducted using the bite of infected mosquitoes, restricting the number of trial sites that can perform CHMI studies. Aseptic, cryopreserved P. falciparum sporozoites (PfSPZ Challenge) provide a potentially more accurate, reproducible and practical alternative, allowing a known number of sporozoites to be administered simply by injection.
Methodology
We sought to assess the infectivity of PfSPZ Challenge administered in different dosing regimens to malaria-naive healthy adults (n = 18). Six participants received 2,500 sporozoites intradermally (ID), six received 2,500 sporozoites intramuscularly (IM) and six received 25,000 sporozoites IM.
Findings
Five out of six participants receiving 2,500 sporozoites ID, 3/6 participants receiving 2,500 sporozoites IM and 6/6 participants receiving 25,000 sporozoites IM were successfully infected. The median time to diagnosis was 13.2, 17.8 and 12.7 days for 2,500 sporozoites ID, 2,500 sporozoites IM and 25,000 sporozoites IM respectively (Kaplan Meier method; p = 0.024 log rank test).
Conclusions
2,500 sporozoites ID and 25,000 sporozoites IM have similar infectivities. Given the dose response in infectivity seen with IM administration, further work should evaluate increasing doses of PfSPZ Challenge IM to identify a dosing regimen that reliably infects 100% of participants.
Trial Registration
ClinicalTrials.gov NCT01465048
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