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Recombinant Adeno-Associated Viral Therapeutics and Gene Doping. How to Detect It?
Natalia V Mesonzhnik1,2, Mikhail B Afonin1, Polina M Novikova1
1Resource Centre of Analytical Methods, Sirius University of Science and Technology, Sochi, Russia.
None:
Gene therapy is a powerful tool for treating and correcting severe genetic diseases caused by defective genes. However, the same technology could be exploited to introduce exogenous genes that enhance physical performance and endurance in sports, which not only subverts the principles of fair competition but also poses risks to athletes' health. Exogenous transgenes can be delivered into the human body via viral vectors, and recombinant adeno-associated virus (rAAV) vectors are, to date, considered the safest and most reliable viral vectors in that regard for a prolonged effect. Since 2003, the World Anti-Doping Agency (WADA) has included the term "gene doping" in its Prohibited List of Substances and Methods under Article M3 "Gene and Cell Doping." To date, no confirmed case of gene doping in sport has been officially identified. Over the past two decades, several strategies for long-term detection of rAAV-based transgenes in biological fluids have been proposed. These include direct methods such as polymerase chain reaction (PCR), liquid chromatography-high-resolution mass spectrometry (LC-HRMS), and matrix-assisted laser desorption/ionization-time-of-flight (MALDI-TOF), and next-generation sequencing (NGS)-based approaches. Indirect methods include detection of recombinant protein products, analysis of immune responses (e.g., neutralizing antibodies, T-cell activation), and "omics" technologies such as proteomics, immunopeptidomics, and metabolomics, as well as combinations thereof. This review aims to provide a general overview of the potential of gene therapy for enhancing athletic performance and methods for detecting rAAV-based gene doping.
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