Inflammation is a highly regulated process involved both in the response to pathogens as well as in tissue homeostasis. In recent years, a complex network of proteins in charge of inflammation control has been revealed by the study of hereditary periodic fever syndromes. Most of these proteins belong to few families and share the capability of sensing pathogen-associated and damage-associated molecular patterns. By interacting with each other, these proteins participate in the assembling of molecular platforms, called inflammasomes, which ultimately lead to the activation of cytokines, to the transcription of inflammatory gene or to the induction of cell apoptosis. Among hereditary periodic fever syndromes, mevalonate kinase deficiency (MKD) is the sole in which the phenotype did not directly associate with a deficiency of these proteins, but with a metabolic defect of the mevalonate pathway, highlighting the importance of this metabolic pathway in the inflammation control. Noteworthy, drugs acting on this pathway can greatly influence the inflammatory response. The modulation of inflammation by mevalonate pathway is of interest, since it may involve mechanisms not directly referable to inflammasomes. MKD provides a robust model to study these mechanisms and possibly to develop new classes of anti-inflammatory drugs.
