circRNA-programmed macrophages enable localized antibody therapy

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Authors: Yawei Du, Daoyu Zhu, Shifeng Ling, Yixuan Chen
Cited by: 1
References: 7

Abstract

Unlike traditional infectious-disease vaccines, mRNA therapeutics offer a far broader application landscape. Among various next-generation mRNA strategies, protein-replacement therapy is particularly promising.1 Although antibodies are widely used clinically, systemic administration often entails notable systemic adverse effects and treatment burden. By contrast, using mRNA to encode and synthesize antibodies in situ within the body confers multiple advantages: (1) achieving sufficient in vivo expression at lower exogenous doses, thereby increasing effective exposure and bioavailability; (2) a highly modular, rapidly iterable manufacturing process with clear cost and scalability benefits; (3) the ability, via delivery systems, to target specific cells or tissues, improving tissue penetration and local action while reducing off-target effects.

Fields of Study & Subjects

RNA Interference and Gene Delivery Circular RNAs in diseases Virus-based gene therapy research

Publication details

Journal / source
Molecular Therapy — Nucleic Acids
Publisher
Elsevier BV
Volume
37
Issue
3
Pages
103010–103010
Publication date
21 July 2026
Language
EN