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“U”敲响丧钟:假尿苷可逃避Toll样受体检测。

For "U" the bell tolls: Pseudouridine evades TLR detection.

作者信息

Young Alexander P, Kanneganti Thirumala-Devi

机构信息

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.

出版信息

Mol Cell. 2025 Sep 4;85(17):3206-3208. doi: 10.1016/j.molcel.2025.08.008.

Abstract

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.

摘要

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。

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