Gene therapy is coming of age. Sarepta’s gene therapy engine provides a framework for potentially creating new therapies for these devastating diseases.
Every gene therapy is comprised of a vector, a promoter, and a transgene, and identifying the appropriate components is critical to developing viable gene therapies. Each component has a role to play:
Vector: Responsible for tissue targeting and delivering the transgene and the promoter to target cells. There are several different types of vectors, including viral vectors such as adenovirus, adeno-associated virus, retrovirus or lentivirus. Other non-viral vectors used in gene therapy include bacterial, lipid- and polymer-based vectors. Patients can potentially have antibodies to some vectors and immune response is important in selecting a vector. Sarepta is currently using adeno-associated virus (AAV) vectors for our gene therapy platform.
Promoter: Responsible for selective gene expression and for driving expression in intended tissue targets.
Transgene: Responsible for producing a functioning version of the protein of interest. The transgene is genetic material introduced into targeted tissues by the vector, and its expression is driven by the promoter.
Vectors used in Sarepta’s gene therapy development programs:
Promoters used in Sarepta’s gene therapy development programs:
The transgenes used in Sarepta’s gene therapy programs vary depending on the disease and protein of interest. Some transgenes contain the full copy of the gene of interest; whereas others contain the partial gene, depending on the gene that is needed.
Sarepta’s gene therapy engine is tailored to specific disease states and aims to select individual components that target specific tissues and cells with the goal of optimizing expression of the select protein in those tissues. Together, these three components form what is called a construct.
As a company on an urgent mission to engineer precision genetic medicine for rare diseases that devastate lives and cut futures short, we want to help answer some frequently asked questions about gene therapy through our educational video series: GT-FAQ. These short videos, hosted by Sarepta researchers, scientists and other employees, answer some of the most common and complex questions about gene therapies in a way we can all understand.
View this video to learn more about how Sarepta is using its investigational, proprietary gene therapy engine to develop gene therapies for specific disease states, aiming to add genes into disease-affected cells with the goal of making a functioning version of the protein that is missing.
Sarepta Therapeutics has brought together the elements essential for successful development of gene therapy—productive collaborations, unparalleled scientific understanding, and an unwavering sense of purpose.
Sarepta has exclusive rights to the SRP-9001 gene therapy program initially developed at the Abigail Wexner Research Institute at Nationwide Children’s Hospital. And in December 2019, Sarepta partnered with Roche to combine Roche’s global reach, commercial presence and regulatory expertise with Sarepta’s gene therapy candidate for Duchenne, SRP-9001, for patients outside the United States. Sarepta is responsible for global development and U.S. commercialization of SRP-9001.
Sarepta’s investigational gene therapy, SRP-9001, follows the 3-part model that drives most gene therapies—vector, transgene, and promoter.
The three elements of Sarepta’s investigational gene therapy for Duchenne:
Sarepta Therapeutics is leveraging our platform approach in gene therapy to research a potential treatment for Duchenne. The information in
this guide provides an overview and answers some frequently asked questions about micro-dystrophin gene therapy.
Sarepta’s 6 development programs focus on: sarcoglycanopathies (LGMD 2C, LGMD 2D, LGMD 2E), dysferlin (LGMD 2B), anoctomin 5 (LGMD 2L), and calpain-3 (LGMD 2A).
The programs for LGMD subtypes 2A, 2E, 2D, 2C, 2B, 2L are being advanced under the guidance of Louise Rodino-Klapac, PhD, Sarepta’s Executive Vice President and Chief Scientific Officer.
You may see variants of LGMD subtype names, as there are several systems in use. Historically, the numerals “1” and “2” have been used to designate the inheritance pattern, followed by a letter indicating the subtypes’ order of discovery. More recently, an alternate system uses the letter “D” for some type-1 dominant inheritance variants, and the letter “R” for some type-2 recessive inheritance variants, plus a number for the order of discovery.
The subtypes are also sometimes referred to by the gene or protein abnormality involved; for example, LGMD2E is also called beta-sarcoglycanopathy because it results from a mutation of the beta-sarcoglycan gene (“-opathy” means a disease or disorder).
The sarcoglycan complex is a subcomplex within the dystrophin-associated glycoprotein complex, consisting of 4 different glycoproteins (gamma, alpha, beta, delta sarcoglycan), which help to maintain sarcolemmal integrity. Mutations in genes encoding one of these four proteins cause LGMD 2C, LGMD 2D, LGMD 2E, and LGMD 2F, respectively.
Phenotypically, sarcoglycanopathy resembles dystrophinopathy, with severe, progressive proximal muscular weakness that leads to early disability. Symptoms may present in early life—typically 4 to 7 years old—and presentation may occur up to the second decade. Respiratory failure and cardiomyopathy (rare in LGMD 2D) are common features and should be actively screened for.
The elements of our investigational gene therapies for the sarcoglycanopathies are as follows:
LGMD 2B (Dysferlinopathy) is a rare, recessively inherited muscular dystrophy caused by mutations in the DYSF gene. The DYSF gene may play an important role in membrane repair.
The clinical phenotype of the dysferlinopathies is quite variable. Clinical symptoms usually start in young adulthood and are associated with highly elevated serum creatine kinase levels. The disease progresses invariably producing muscle weakness that markedly impairs daily activities and dramatically reduces quality of life.
The elements of our investigational gene therapy for LGMD 2B dysferlinopathy (LGMD R2) are:
An autosomal recessive mutation in the gene coding for anoctamin 5 causes limb-girdle muscular dystrophy type 2L (LGMD R12). Anoctamin 5 has been shown to be critical for membrane repair, but how it functions in the membrane repair complex remains unknown.
This condition is characterized by proximal weakness affecting the pelvic girdle and leg muscles, or with only distal weakness known as non-dysferlin Miyoshi muscular weakness type 3 (MMD3). Asymmetric weakness is relatively common in which prominent asymmetrical atrophy of the quadriceps femoris and biceps brachii is the diagnostic hallmark.
The elements of our investigational gene therapy for LGMD 2L anoctaminopathy are:
CAPN3 gene encodes a muscle-specific, calcium-activated neutral protease, calpain-3, that binds to titin and dysferlin and plays a major role in sarcomere remodeling.
Calpainopathy is characterized by symmetric and progressive weakness of proximal limb-girdle muscles. The age at onset of muscle weakness ranges from two to 40 years. Clinical findings of calpainopathy include the tendency to walk on tiptoes, difficulty in running, scapular winging, waddling gait, and slight hyperlordosis. Loss of ambulation typically occurs from 5 to 39 years of age.
The elements of the investigational gene therapy for LGMD 2A calpainopathy are:
The pioneering research of Louise Rodino-Klapac, Ph.D, our Executive Vice President, Head of R&D and Chief Scientific Officer, is the foundation for five of our investigational limb-girdle muscular dystrophy (LGMD) programs. Hear from Dr. Rodino-Klapac about the science behind the LGMDs, the importance of subtype identification and how our gene therapy engine will help engineer potential therapies for this group of inherited neuromuscular diseases.
Sarepta, along with our collaborator, Zarife Sahenk, MD, PhD, from Nationwide Children’s Hospital, is developing neurotrophin 3 (NT-3), a gene therapy candidate designed to treat CMT, with the lead indication being type 1A.
Schwann cells (SCs) play a crucial role in the support of axonal regeneration and associated myelination. Our hypothesis is that mutations interfere with the ability of SCs to differentiate into a competent state to support axonal growth and myelination. Schwann cell survival and differentiation factor, NT-3, could potentially overcome these deficiencies.
This investigational compound is designed to deliver a neurotrophin NTF3 transgene.
The three elements of Sarepta's investigational gene therapy for CMT are:
NT-3 gene therapy in development also has the potential to treat other subtypes of CMT, along with other muscle-wasting disorders.