Gene therapy for monogenic liver diseases: clinical successes, current challenges and future prospects

Over the last decade, pioneering liver-directed gene therapy trials for haemophilia B have achieved sustained clinical improvement after a single systemic injection of adeno-associated virus (AAV) derived vectors encoding the human factor IX cDNA. These trials demonstrate the potential of AAV technology to provide long-lasting clinical benefit in the treatment of monogenic liver disorders. Indeed, with more than ten ongoing or planned clinical trials for haemophilia A and B and dozens of trials planned for other inherited genetic/metabolic liver diseases, clinical translation is expanding rapidly. Gene therapy is likely to become an option for routine care of a subset of severe inherited genetic/metabolic liver diseases in the relatively near term. In this review, we aim to summarise the milestones in the development of gene therapy, present the different vector tools and their clinical applications for liver-directed gene therapy. AAV-derived vectors are emerging as the leading candidates for clinical translation of gene delivery to the liver. Therefore, we focus on clinical applications of AAV vectors in providing the most recent update on clinical outcomes of completed and ongoing gene therapy trials and comment on the current challenges that the field is facing for large-scale clinical translation. There is clearly an urgent need for more efficient therapies in many severe monogenic liver disorders, which will require careful risk-benefit analysis for each indication, especially in paediatrics

HPLC DETERMINATION OF VITAMIN A PALMITATE: UNEQUIVALENCE OF QUANTITATIVE ANALYSIS PERFORMED BY DIRECT AND REVERSE PHASE MODE

COMUNICAZIONE ORALE OC 2

A 1,5-DIARYLPYRROLE DERIVATIVE

The structure of the 1,5-diarylpyrrole derivative, ethyl 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-2-methyl-3-pyrrolecarboxylate, C20H16Cl3NO2, has been determined. The orientation assumed by the phenyl rings corresponds to the deepest of the two minima obtained from ab initio calculations. All bond distances and angles are in the expected ranges

INTERACTION OF RETINYL PALMITATE WITH PHOSPHOLIPID AND NON-PHOSPHOLIPID VESICLES.

POSTER PA 1