| Popis: |
The human immune system is one of the most important causative factors in the pathogenesis of various chronic inflammatory diseases. The network of immunoregulatory signals ruling the course of such disorders is highly complex and does not only involve the cells of the immune system, but also those of the diseased organs. This makes it rather difficult to model such regulatory processes in vitro. Most existing cell culture systems suffer from a serious lack of complexity. This is one of the major reasons why the majority of drug candidates fail in patients. Drugs that are meant to mono-specifically counter-regulate a disease process tend to develop unpredictable responses, due to unknown crosslinks in signalling pathways that are not available in simple culture models. Thus, the candidate selection as it is used at present, can be improved substantially by using more elaborate, in-vivo-like human cell culture models. Such test systems will accelerate the drug development process and decrease the risk of candidate failure. This review describes a new set of human organotypic, reproducible routine cell culture models, developed to optimise the drug candidate selection process and to increase clinical success rates. It is expected that models like these will accelerate drug development in the future substantially. |
