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2025/12/10
📅 Dec 8 - 14, 2025
Children's Hospital of Philadelphia completed the first personalized CRISPR gene-editing therapy for sickle cell disease. Unlike Casgevy (FDA-approved last year), this new approach uses patient-specific editing strategies targeting the exact mutation causing the disease, rather than the universal fetal hemoglobin reactivation pathway.
Key Highlights:
Beam Therapeutics announced that its base-edited CAR-T therapy BEAM-201 received FDA Breakthrough Therapy Designation for relapsed/refractory T-cell acute lymphoblastic leukemia (T-ALL). This therapy uses base editing technology (rather than traditional CRISPR cutting) for multiplex editing of donor T cells, creating an "off-the-shelf" CAR-T product.
Technical Advantages:
Nature Neuroscience published important research revealing a new mechanism by which mutant huntingtin protein (mHTT) causes neuronal death in Huntington's disease. The research team discovered that mHTT disrupts mitochondria-ER contact sites (MAMs), leading to calcium homeostasis imbalance, providing a crucial target for developing new therapeutic strategies.
Research Significance:
The David Baker laboratory published new results in Science, demonstrating novel protein nanocages designed using RFdiffusion that can precisely encapsulate and release drug molecules. These nanocages can undergo controlled switching in response to pH changes or specific ligands, opening new pathways for targeted drug delivery.
Application Prospects:
Synlogic announced that its engineered E. coli strain SYNB1934 has entered Phase III clinical trials for treating inflammatory bowel disease (IBD). This genetically modified strain can locally produce anti-inflammatory molecules IL-10 and short-chain fatty acids in the gut, achieving precision-targeted therapy.
Innovation Features:
FieldEventImpact🏛️ PolicyUS BIOSECURE Act advances in House voteRestricts collaboration with certain foreign biotech companies💰 FundingRecursion Pharmaceuticals completes $500M financingAccelerates AI drug discovery platform expansion🤝 PartnershipRoche and Flagship Pioneering reach $2B collaborationDevelop next-generation cell therapies📈 IPOAutobahn Therapeutics lists on NASDAQRaises $180M for neurological disease programs
Multiple studies this week advance the "biological computing" concept:
New tools for regulating gene expression without altering DNA sequence:
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This digest is compiled from public information for reference only