<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Crispr on BRYSGO</title><link>https://www.brysgo.com/tags/crispr/</link><description>Recent content in Crispr on BRYSGO</description><generator>Hugo</generator><language>en-us</language><lastBuildDate>Thu, 04 Jun 2026 14:26:16 +0000</lastBuildDate><atom:link href="https://www.brysgo.com/tags/crispr/index.xml" rel="self" type="application/rss+xml"/><item><title>The Immune Problem Was Always the Problem: How Engineered "Stealth" Beta Cells Finally Address It</title><link>https://www.brysgo.com/post/2026-06-04-the-immune-problem-was-always-the-problem-how-engineered-stealth-beta-/</link><pubDate>Thu, 04 Jun 2026 14:26:16 +0000</pubDate><guid>https://www.brysgo.com/post/2026-06-04-the-immune-problem-was-always-the-problem-how-engineered-stealth-beta-/</guid><description>&lt;p&gt;Islet transplantation has worked as a diabetes treatment for decades. The procedure itself isn&amp;rsquo;t the problem — surgeons can take insulin-producing cells from a donor pancreas, infuse them into the hepatic portal vein, and watch a Type 1 diabetic patient achieve near-normal blood glucose without injecting insulin. It&amp;rsquo;s been demonstrated repeatedly since the Edmonton Protocol in 2000. The reason it never became standard care has nothing to do with the transplant. It&amp;rsquo;s what comes after: to keep those cells alive in a foreign body, patients need immunosuppression aggressive enough to cause kidney damage, increase cancer risk, and leave them vulnerable to infections that can kill them. You&amp;rsquo;re trading one chronic disease for a cocktail of others.&lt;/p&gt;</description></item></channel></rss>