New way to improve the efficacy of innovative RNA therapies
Peer-Reviewed Publication
Updates every hour. Last Updated: 17-Dec-2025 14:22 ET (17-Dec-2025 19:22 GMT/UTC)
A recent study involving researchers from the University of Basel reveals that slowing down the intracellular transport of RNA-based drugs can significantly enhance their effectiveness. These promising therapeutics are currently used to treat rare genetic diseases.
Senescent cells, which are damaged and inflammatory, contribute significantly to ageing. Researchers at the Max Planck Institute for Biology of Ageing have found that worms can enter a senescent-like state, similar to that observed in mammals. This discovery provides a simple yet powerful model to study senescence at the whole organism level, enabling the identification of new ways to prevent or reverse senescence. These findings hold promise for developing therapies targeting age-related conditions and cancer dormancy.
Using a cell-free RNA (cfRNA) “liquid biopsy” of maternal plasma, researchers at the Carlos Simon Foundation and iPremom enrolled 9,586 pregnant women from 14 hospitals across Spain between September 2021 and June 2024. In a nested case-control analysis of 216 participants, they successfully predicted both early-onset and late-onset preeclampsia well before the onset of symptoms.
By isolating paternal age from female reproductive factors through the exclusive use of donor eggs from young women, the study provides robust evidence that male age plays a critical role in reproductive success, challenging the common assumption that sperm age has little impact once fertilisation occurs.