<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Cell-Therapy on 生物经济</title><link>https://cn.bioecon.ru/technologies/cell-therapy/</link><description>Recent content in Cell-Therapy on 生物经济</description><generator>Hugo</generator><language>zh-CN</language><lastBuildDate>Sat, 11 Jul 2026 14:19:14 +0700</lastBuildDate><atom:link href="https://cn.bioecon.ru/technologies/cell-therapy/index.xml" rel="self" type="application/rss+xml"/><item><title>NK 细胞与 CAR-NK 疗法</title><link>https://cn.bioecon.ru/technology/nk-cell-car-nk-therapy/</link><pubDate>Fri, 19 Jun 2026 00:00:00 +0000</pubDate><guid>https://cn.bioecon.ru/technology/nk-cell-car-nk-therapy/</guid><description>CAR-NK 与 NK 细胞疗法 — 对抗实体瘤和血液肿瘤的同种异体、现货型效应细胞，具有低毒性（极少 CRS，无 GVHD）；iPSC-NK 是可扩展的平台。</description></item><item><title>TIL 疗法（肿瘤浸润淋巴细胞）</title><link>https://cn.bioecon.ru/technology/til-therapy/</link><pubDate>Fri, 19 Jun 2026 00:00:00 +0000</pubDate><guid>https://cn.bioecon.ru/technology/til-therapy/</guid><description>TIL 疗法——具有多克隆特异性的自体肿瘤浸润 T 细胞；首个获批药物 Lifileucel（Amtagvi，Iovance，FDA 2024）是转移性黑色素瘤的突破。</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>