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Beyond “One disease at a time”: Therapeutic platforms for rare monogenic disease
Based on the most recent estimates, there are over 10,000 known human diseases, and more are being discovered each day. A large fraction of these are rare monogenic (Mendelian) disorders. Gene-targeted therapies, such as gene therapy, gene editing, and oligonucleotides are therapeutic platforms that are broadly applicable to a large fraction of monogenic diseases. However, these technologies are currently developed as treatments for one disease at a time. This approach favors the most common rare diseases, and will leave many diseases and patients who could greatly benefit from gene targeted therapies behind. To address this disparity, a fundamentally different way of thinking about the problem is required. One potential solution, based on the science itself, is to develop gene-targeted therapies as therapeutic platforms to treat monogenic disease, rather than as treatments for one disease at a time. I will discuss the implications and challenges of this approach and provide examples of ongoing research in this area. See pave-gt.ncats.nih.gov ; fnih.org/our-programs/AMP/BGTC ; commonfund.nih.gov/editing .
Date:
23 June 2023, 15:00
Venue:
IMS-Tetsuya Nakamura Building, Roosevelt Dr, Headington OX3 7TY
Venue Details:
IDRM Seminar Rooms 1&2
Speaker:
Dr Philip J. (P.J.) Brooks (NIH)
Organiser:
Associate Professor Carlo Rinaldi (University of Oxford, MDUK Oxford Neuromuscular Centre)
Organiser contact email address:
rufina.kaloyanova@medsci.ox.ac.uk
Host:
Associate Professor Carlo Rinaldi (University of Oxford, MDUK Oxford Neuromuscular Centre)
Part of:
IDRM Seminar Series
Booking required?:
Required
Booking email:
rufina.kaloyanova@medsci.ox.ac.uk
Audience:
Members of the University only
Editor:
Rufina Kaloyanova
