On Friday, President Donald Trump announced "Operation Warp Speed," a partnership between the government and pharmaceutical companies to develop, manufacture and distribute hundreds of millions of doses of a COVID-19 vaccine by the end of 2020. Comparing the effort to the Manhattan Project that produced the atomic bomb, Trump acknowledged that the plan would be "risky and expensive."
And while the timing may offer hope to those tired of social distancing and help his re-election campaign, the timeline for Operation Warp Speed is likely unrealistically ambitious. There are even questions about the scientific feasibility of making an effective vaccine — not just this year, but in the near future.
While on Monday biotech company Moderna reported promising results from early human trials for one potential coronavirus vaccine, we shouldn't lose sight of the fact that there are miles to go before we have millions of doses of an effective vaccine. The history of large-scale, international efforts to develop and distribute vaccines has produced mixed results. Some, like the polio vaccine and the eradication of smallpox, were quite successful. Many others, despite decades of scientific focus and billions of dollars in investment, were not.
These failures — as well as the relative success of low-tech prevention strategies and drugs that treat virus patients — show the advantages of fighting the pandemic in a balanced way, one that combines the quest to develop a vaccine with efforts more likely to pay off.
Scientists have been trying to make a vaccine for malaria since the late 1960s. Pharmaceutical giant GlaxoSmithKline has had one candidate in development since 1984, known as RTS,S, that it developed in collaboration with the Walter Reed Army Institute of Research. The research program got a boost in 1999, when the Bill and Melinda Gates Foundation launched the Malaria Vaccine Initiative with a $50 million grant.
Managed by PATH, a Seattle-based global health nonprofit, the Malaria Vaccine Initiative has partnered with GlaxoSmithKline since 2001 to refine the RTS,S vaccine. Yet, despite this costly push that brought together public and private resources, more than 30 years since its initial development, the vaccine is still less than 40% effective and efficacy has been shown to wane over time.
While many scientists remain optimistic about the prospects of an eventual malaria vaccine, there are many challenges. There are four different species of malaria, each with several different genetic strains. In addition, the malaria parasite goes through distinct life-cycle stages in the course of infecting the human body and reproducing in the bloodstream, so any vaccine would need to be able to target multiple stages of the parasite's reproduction. This complexity spotlights why vaccines can be so hard to develop — even when there is real urgency and a significant commitment of resources.
Indeed, malaria remains one of the leading causes of death globally, where it is endemic in many low-income countries despite large-scale eradication efforts throughout the 20th century and the availability of low-tech, but effective, preventive measures like insecticide-treated bed nets that reach too few at-risk people thanks to a lack of resources and long-term community engagement.