Sygnature Discovery has established an in vivo LPS model of inflammation which can help understand life-limiting neuroinflammatory conditions like Parkinson’s disease, multiple sclerosis, Alzheimer’s disease, and traumatic brain injuries and identify new drug targets.
The LPS in vivo model supports early-stage anti-inflammatory drug discovery in neuroinflammation, kidney, and systemic inflammation. The inclusion of kidney inflammation and neuroinflammation studies in Sygnature Discovery's LPS model sets it apart from conventional models, providing valuable insights into the complex interplay of inflammation in different organs.
This unique capability enables researchers to identify new drug mechanisms, evaluate drug efficacy, and enhance our understanding of kidney and neuroinflammatory diseases, driving the downstream development of targeted therapeutic interventions for patients with unmet needs. The model also enables an understanding of the pharmacology and processes that underpin systemic inflammation, and builds on existing in vitro capabilities within Sygnature Discovery to further strengthen drug target validation and translation from in vitro to in vivo. It measures key pro-inflammatory cytokines in blood and provides a useful model system to quickly evaluate the efficacy of novel anti-inflammatory drugs in early drug discovery.
Commenting on the model’s benefits Dr. John Unitt, Vice President of Inflammation and Immunology at Sygnature Discovery, said: “An important step in drug discovery is the successful translation of a drug's effect on in vitro cell function to efficacy in an in vivo disease model. Sygnature's LPS in vivo model provides that initial step in determining the efficacy of a novel anti-inflammatory. Getting this first in vivo inflammation model off the ground is an exciting start, but it is only the beginning of a pipeline of new models planned to test a broader range of immunomodulatory drugs and mechanisms.”