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Intermediate

Delivery: the real bottleneck

Getting the editing machinery into the right cells, in enough of them, without harm — the problem that decides which diseases are treatable.

要約

People imagine the hard part of gene editing is the editing. It is not. The hard part is getting the machinery into the right cells inside a living body. We can reach the liver reliably, the eye and blood cells with more effort, and muscle, brain and lung barely at all. Almost every disease that looks 'nearly solved' but never arrives is stuck on this.

Delivery determines tissue tropism, dose, immunogenicity and duration of editor exposure. Lipid nanoparticles achieve efficient hepatocyte delivery and are transient, favouring safety. AAV offers broad tropism with engineered capsids but has a ~4.7 kb packaging limit, provokes pre-existing and induced immunity, and causes dose-dependent hepatotoxicity that has been fatal at high systemic doses. Ex vivo electroporation of ribonucleoprotein avoids systemic exposure entirely but requires conditioning and cell manufacturing.

What each route can and cannot reach

RouteReachesMain limitation
Lipid nanoparticleLiver, very efficientlyLittle else, without targeting innovations
AAVEye, liver, some muscle and central nervous systemSize limit; immunity; toxicity at high doses
Ex vivo electroporationBlood and immune cellsRequires conditioning chemotherapy and manufacturing
Inhaled deliveryAirway, in principleMucus and epithelial defences; largely preclinical
Direct injectionEye, some local tissueOnly where a needle can go

This table is effectively a map of which diseases have clinical programmes and which do not.

Sources

Connected in the Atlas

Every entry on this site is linked to the others it relates to. These connections are part of the record, not a search result.