Technology, injections & supplies

Fourteen months on, no anti-rejection drugs: Sana’s cells keep going

Breakthrough T1D UK reported Sana’s gene-engineered islet cells were still making insulin at 14 months, without anti-rejection drugs.

Written by Updated 16 March 2026 2 min read
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The 60-second answer

You can file this under real progress that still does not change your day. In Sana’s early study, one patient still had working, gene-engineered insulin-making cells at 14 months, without any anti-rejection drugs. That last part is the point: today’s islet transplants need those harsh, lifelong drugs, so they are kept for the most severe cases.

  • Islet cells are the clusters in the pancreas holding the beta cells that make insulin; in Type 1 the immune system destroys them.
  • Islet transplants exist on the NHS but rely on anti-rejection drugs (they dampen the immune system) that carry real risks, so they are rare.
  • Sana engineered its cells to be harder to spot, and at 14 months they were still alive and making insulin without those drugs.
  • This is a single participant, so it shows the idea can last over time, not that it works for everyone yet.
The update

What 14 months adds to the story

This is the same Sana study NPN has followed before: first the cells survived four weeks, then six months, and now Breakthrough T1D UK reports they were still evading the immune system and making insulin at 14 months. Why does the calendar matter so much? Because a cure has to last. Cells that work for a month but fade within a year would not free anyone from insulin. Each longer time point is a small piece of evidence that the engineering, making the cells less visible to the immune system, is holding up rather than slowly failing. That is genuinely encouraging.

The honest bar

Why this is still years away

One participant is not a trial you can draw firm conclusions from. Researchers will need to repeat this in more people, follow them for longer, and show it is both safe and reliable before anyone talks about routine use. The amount of cells given here was part of an early safety study, too, not a full transplant designed to end insulin injections. So the fair summary is this: a real and important signal that immune-invisible cells can last, sitting inside a process that still has larger trials, regulators and NHS decisions ahead of it. Hope is reasonable. A countdown is not.

What to notice

Worth keeping in perspective

Early cure research is often reported one patient at a time; a strong single case is a start, not a finish.
The advance being tested here is avoiding anti-rejection drugs, which is exactly what makes today’s islet transplants so limited.
If you want to follow it, UK charities like Breakthrough T1D and Diabetes UK are steadier than one-off headlines.
What to ask your team

Questions that make an appointment useful

"Is islet or pancreas transplantation ever something that would apply to my situation, and what would make someone eligible?"
"Are there any UK research studies in this area I could register my interest in?"
Sources