Young Alexander P, Kanneganti Thirumala-Devi
Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Mol Cell. 2025 Sep 4;85(17):3206-3208. doi: 10.1016/j.molcel.2025.08.008.
TLRs detect pathogen-derived uridine but not endogenous pseudouridine, which promotes host defense without autoimmunity. This principle is critical for the safe design of mRNA-based therapeutics, but the underlying mechanisms driving differential innate immune activation were unknown. In a recent issue of Cell, Bérouti et al. find that pseudouridine-containing RNA resists enzymatic degradation to evade TLR-mediated inflammation and type I interferon response.
Toll样受体(TLRs)能检测病原体来源的尿苷,但不能检测内源性假尿苷,内源性假尿苷可促进宿主防御而不引发自身免疫。这一原理对于基于信使核糖核酸(mRNA)的治疗药物的安全设计至关重要,但驱动不同先天免疫激活的潜在机制尚不清楚。在最近一期的《细胞》杂志上,贝鲁蒂等人发现含假尿苷的核糖核酸(RNA)能抵抗酶促降解,以逃避TLR介导的炎症和I型干扰素反应。