Can we edit our genes to outsmart the pathogens that shaped our evolution?

The Future of Immunity - Robin May · 51:29 · Video: Gresham College · Watch at the source

In short: For millennia, our survival depended on inherited genetic luck against lethal infections. Today, we stand at a threshold where human innovation, from precision medicine to CRISPR gene editing, allows us to actively modify our immune defenses. Are we moving toward a disease-free future or crossing an irreversible ethical line?

Humanity has spent millions of years locked in an evolutionary arms race with pathogens. Because infectious diseases were the primary cause of death throughout our history, our immune genes have been under intense selective pressure. Modern genomic analysis confirms this, revealing that the fastest-evolving regions of the human genome are almost exclusively linked to immune function. We are the descendants of survivors who possessed the right genetic tools to endure these threats.

A striking example of this selection occurred during the 14th-century bubonic plague. Estimates suggest the Black Death killed between 30% and 60% of the European population. This massive mortality event left a clear signal in the survivor population, with specific gene variants that helped fight the bacterium Yersinia pestis rising rapidly in frequency. Today, we continue to see the impact of such history; even in the modern era, genetic variation remains a major factor in how individuals respond to infections like Covid-19.

We are now transitioning from relying on natural selection to taking control of our own biology. In 2024, the UK became the first nation to approve a medicine using CRISPR/Cas9 technology to correct a mutation causing debilitating blood disorders. While currently costly and limited, this precision editing could eventually address complex immune disorders or viral susceptibility. This capability offers immense medical promise but forces us to confront the profound ethical dilemma of making heritable changes that would permanently alter the human genome for future generations.

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