RNA-based medicines are a class of treatments that leverage RNA molecules to target and modulate gene expression for therapeutic purposes. This field has gained significant attention due to its promise in treating a wide array of diseases, including cancer, genetic disorders, and viral infections. As the demand for RNA-based therapeutics continues to rise, maintaining the purity, stability, and efficacy of these RNA products is essential for clinical applications.
A critical challenge in the development of RNA-based therapies is the presence of unintended impurities, particularly double-stranded RNA (dsRNA). While dsRNA is an inevitable byproduct of in vitro transcription (IVT), uncontrolled contamination can pose serious risks. They can trigger potent immune responses through innate immune pathways, such as the activation of toll-like receptors (TLRs), and can lead to inefficient translation of therapeutic mRNA or circRNA. These unintended interactions reduce therapeutic efficacy.
Researchers and manufacturers in the field are developing robust strategies and analytical methods to minimize dsRNA presence, ensuring that the final RNA product is both safe and capable of achieving its intended therapeutic goals.
Double-stranded RNA is a structural form of RNA that consists of two complementary strands bound together in a helical formation. In mRNA manufacturing, dsRNA emerges as a byproduct of the IVT process, where RNA polymerases synthesize mRNA from a DNA template.
The undesired impurity results from:
Secondary structures or hairpins are formed by self-complementary sequences.
Transcription errors, specifically incomplete termination or re-initiation.
Antisense RNA, created from the opposite DNA strand, hybridizes with the sense mRNA.
The presence of dsRNA in mRNA-based medicine has several risks:
Innate Immune Activation – dsRNA is recognized as a viral signature by the innate immune system, mainly via pattern recognition receptors (PRRs) like Toll-like receptor 3 (TLR3) and retinoic acid-inducible gene I (RIG-I). This can lead to excessive immune activation, resulting in inflammation, reduced therapeutic efficacy, and potential safety concerns. Controlling dsRNA is key for vaccine production.
Reduced Protein Expression – The cell’s machinery degrades dsRNA, reducing the amount of mRNA available for translation and leading to lower protein output. In mRNA therapeutics, this results in diminished therapeutic effects.
Batch-to-Batch Variability – Inconsistent dsRNA removal strategies can introduce variability in manufacturing, making it challenging to achieve reproducible clinical outcomes.
At CATUG, we understand the critical importance of dsRNA detection and control in RNA manufacturing. We use several analytical and detection methods to detect dsRNA impurities with superior sensitivity, including:
dsRNA-specific ELISA assays
Electrophoretic separation with our proprietary dsRNA ladders
Next-generation sequencing and chromatography
State-of-art proprietary technology to analyse and purify RNA products.
Check our webinar at the USP mRNA Virtual Summit about CATUG's analytical methods for dsRNA detection in IVT mRNA by our Director of Analytical Development Department, Dr. Michael Zhang.
Double-strand RNA standards and ladders are used by researchers to benchmark and quantify dsRNA impurities with high accuracy. With these tools you can:
Reliably assess dsRNA contamination at various stages of production.
Standardized calibration for quality control testing.
Compare across different manufacturing conditions to optimize purification steps.
Purchase our dsRNA standards and ladders.
The next generation of RNA therapeutics should be safer, more effective, and consistently high-quality. Our manufacturing methods ensure:
High-yield, high-purity RNA products.
Reduced immunogenicity without compromising stability or expression.
Compliance with regulatory expectations for RNA therapeutics.
Get RNA products with minimal dsRNA content.