Global Catastrophic Biological Risks (GCBRs)—such as engineered pathogens or novel viruses—pose a severe threat to humanity. Current medical countermeasures often fail against these risks because they are too specific or can be easily bypassed by adversarial engineering. There’s a pressing need for adaptable, robust solutions that can quickly respond to unknown or deliberately designed biological threats.
One way to address GCBRs could involve two complementary strategies:
The goal would be to ensure these countermeasures remain effective even if a pathogen is deliberately modified to evade them.
Governments, biodefense agencies, and pharmaceutical companies could benefit from such technologies. Governments might see it as a national security priority, while private firms could license the platforms for commercial use. A phased approach could start with a minimal viable product (MVP), like a rapid mRNA-based vaccine platform, followed by testing against engineered threats and eventual integration into public health infrastructure.
While the idea offers significant advantages—like adaptability and adversarial robustness—it also carries risks, such as potential misuse. Strict access controls, ethical oversight, and collaboration with biosecurity experts could help mitigate these concerns. Existing efforts, like DARPA’s Pandemic Prevention Platform or Moderna’s mRNA technology, provide a foundation, but this proposal would extend their capabilities by explicitly accounting for engineered threats.
By focusing on scalable, adaptable solutions, this approach could help close critical gaps in global biodefense preparedness.
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