Infection-Treatment-Vaccination for Plasmodium Falciparum

Brief Summary

Detailed Description

This randomized, partial double-blind, placebo-controlled phase 1 study is designed to evaluate whether sterile protective immunity to P. falciparum can be induced by wild-type (non-attenuated) sporozoite immunizations when exposure is limited to sporozoite and early liver stage of the parasite life cycle and at a low dose sporozoite inoculum relative to other whole parasite vaccination models using live attenuated P. falciparum parasites (e.g. irradiated sporozoites). A secondary objective of the study is to evaluate newly identified antigens as potential targets of an immune response preferentially induced in individuals protected by whole sporozoite vaccination. Once identified as immune targets, these antigens can then be prioritized for subunit vaccine development. Subjects will be closely monitored for signs and symptoms of malaria and/or drug toxicity throughout the study. A total of 36 healthy, malaria-naive adult subjects will be enrolled in the study. Six subjects will be randomized to the Pilot Phase (Arm 1), 24 to the Main ITV Phase (Arms 2, 3, and 4), and six subjects will be randomized for challenge control (Arm 5) to start on the day of challenge of the Challenge Phase. Subjects in Arms 1-4 will receive three episodes of ITV immunization and a subsequent challenge with homologous P. falciparum sporozoites in the absence of chemoprophylaxis. The ITV immunization in this study consists of: 1. Experimental infection with wild-type (non-attenuated) NF54 strain P. falciparum sporozoites delivered by the bites of 12 - 15 infected A. stephensi mosquitoes (ITV infection) administered in conjunction with 2. Causal prophylaxis with PQ or placebo, timed to eliminate parasites early in the liver stage of development, after hepatocyte invasion but prior to maturation and release into the bloodstream, and 3. Continuous suppressive prophylaxis with the blood-stage antimalarial drug CQ to prevent development of patent parasitemia and clinical malaria. The study includes a Pilot Phase because the timing of PQ dosing relative to parasite exposure is critical to the efficacy of PQ as causal prophylaxis yet still allowing for maximized antigenic exposure to liver-stage parasites. The Pilot Phase will compare the prevention of blood-stage parasitemia by PQ administered two days vs. three days after a single ITV infection. Based on protection data from the Pilot Phase, a dosing algorithm will be used to determine timing of the PQ dose for the Main ITV Phase. In the Challenge phase, which occurs after the three ITV events, sterile protective immunity will be assessed by challenge with homologous P. falciparum sporozoites in the absence of chemoprophylactic drugs. Five weeks after stopping chemoprophylaxis, subjects will undergo experimental P. falciparum infection by the bites of five infective mosquitoes and will be closely monitored for signs and symptoms of malaria in a hotel setting. Subjects who develop patent parasitemia will be immediately treated with a standard dose of Malarone and withdrawn from the study. Treated subjects will continue to be monitored with daily blood smears until three consecutive daily blood smears are negative and any residual symptoms of malaria are mild or resolved. Subjects are closely monitored throughout the study for solicited and unsolicited adverse events related to any part of the ITV immunization. The study is expected to last 4 to 9 months depending on which the subject is assigned, and may have up to 64 scheduled study visits during the time period. Subjects will be followed in the clinic for 35 days after the challenge and a follow up phone call will be conducted at six months after the challenge. In an effort to evaluate the duration of an immune response to ITV, all subjects will be invited to return for optional evaluations at three and six months post challenge.

Primary Outcomes

Secondary Outcomes

• ELISA(up to 182 days)
• IFN-y ELISPOT(up to 182 days)
• ICS assay(up to 182 days)