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The **prime-and-trap vaccine** is an experimental, preclinical heterologous malaria vaccine strategy designed to induce durable, protective liver-resident memory CD8+ T (Trm) cells. Developed by the University of Washington, MalarVx, and HDT Bio, the two-step regimen first primes the immune system with a nucleic acid vaccine (either DNA or self-replicating RNA, the latter formulated in HDT Bio's LION cationic nanocarrier) encoding the Plasmodium circumsporozoite protein (CSP). The second step delivers a single 'trapping' dose of radiation-attenuated sporozoites (RAS) that home to the liver, attracting and trapping the primed CD8+ T cells there to eliminate liver-stage Plasmodium parasites and provide sterile protection. Preclinical studies in mice have demonstrated high levels of sterilizing protection, and efforts are underway to translate the strategy to human clinical trials.
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