<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Aav-Vectors on 生物经济</title><link>https://cn.bioecon.ru/technologies/aav-vectors/</link><description>Recent content in Aav-Vectors on 生物经济</description><generator>Hugo</generator><language>zh-CN</language><lastBuildDate>Thu, 23 Jul 2026 23:05:33 +0700</lastBuildDate><atom:link href="https://cn.bioecon.ru/technologies/aav-vectors/index.xml" rel="self" type="application/rss+xml"/><item><title>体内基因治疗：AAV与慢病毒载体</title><link>https://cn.bioecon.ru/technology/gene-therapy-in-vivo-aav-lentiviral/</link><pubDate>Thu, 23 Jul 2026 00:00:00 +0000</pubDate><guid>https://cn.bioecon.ru/technology/gene-therapy-in-vivo-aav-lentiviral/</guid><description>通过工程化腺相关病毒与慢病毒载体将功能性治疗基因一次性递送进患者细胞——自2017年Luxturna以来已有八款FDA批准的体内产品，从Luxturna到Beqvez，如今已是与诚实的商业收缩并存的数十亿美元临床现实。</description></item><item><title>个性化与再生医学</title><link>https://cn.bioecon.ru/technology/personalized-regenerative-medicine/</link><pubDate>Fri, 19 Jun 2026 00:00:00 +0000</pubDate><guid>https://cn.bioecon.ru/technology/personalized-regenerative-medicine/</guid><description>针对罕见单基因病和肿瘤疾病的基因与细胞治疗平台：AAV载体、慢病毒HSC编辑、体外CRISPR（Casgevy）和体内CRISPR（LNP递送）已获FDA和EMA批准，可实现持久的单次给药治疗。</description></item></channel></rss>