TY - JOUR
T1 - Adeno-Associated Virus (AAV) gene therapy for cystic fibrosis
T2 - current barriers and recent developments
AU - Guggino, William B.
AU - Cebotaru, Liudmila
N1 - Funding Information:
The authors are funded by NIH grant R01 HL122267 and grant GUGGIN14P0 from the Cystic Fibrosis Foundation.
Publisher Copyright:
© 2017 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2017/10/3
Y1 - 2017/10/3
N2 - Introduction: Since the cystic fibrosis (CF) gene was discovered in 1989, researchers have worked to develop a gene therapy. One of the most promising and enduring vectors is the AAV, which has been shown to be safe. In particular, several clinical trials have been conducted with AAV serotype 2. All of them detected viral genomes, but identification of mRNA transduction was not consistent; clinical outcomes in Phase II studies were also inconsistent. The lack of a positive outcome has been attributed to a less-than-efficient viral infection by AAV2, a weak transgene promoter and the host immune response to the vector. Areas covered: Herein, the authors focus on AAV gene therapy for CF, evaluating past experience with this approach and identifying ways forward, based on the progress that has already been made in identifying and overcoming the limitations of AAV gene therapy. Expert opinion: Such progress makes it clear that this is an opportune time to push forward toward the development of a gene therapy for CF. Drugs to treat the basic defect in CF represent a remarkable advance but cannot treat a significant cohort of patients with rare mutations. Thus, there is a critical need to develop a gene therapy for those individuals.
AB - Introduction: Since the cystic fibrosis (CF) gene was discovered in 1989, researchers have worked to develop a gene therapy. One of the most promising and enduring vectors is the AAV, which has been shown to be safe. In particular, several clinical trials have been conducted with AAV serotype 2. All of them detected viral genomes, but identification of mRNA transduction was not consistent; clinical outcomes in Phase II studies were also inconsistent. The lack of a positive outcome has been attributed to a less-than-efficient viral infection by AAV2, a weak transgene promoter and the host immune response to the vector. Areas covered: Herein, the authors focus on AAV gene therapy for CF, evaluating past experience with this approach and identifying ways forward, based on the progress that has already been made in identifying and overcoming the limitations of AAV gene therapy. Expert opinion: Such progress makes it clear that this is an opportune time to push forward toward the development of a gene therapy for CF. Drugs to treat the basic defect in CF represent a remarkable advance but cannot treat a significant cohort of patients with rare mutations. Thus, there is a critical need to develop a gene therapy for those individuals.
KW - Gene therapy
KW - adeno-associated virus
KW - clinical trials
KW - cystic fibrosis
KW - preclinical testing
UR - http://www.scopus.com/inward/record.url?scp=85028741968&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85028741968&partnerID=8YFLogxK
U2 - 10.1080/14712598.2017.1347630
DO - 10.1080/14712598.2017.1347630
M3 - Review article
C2 - 28657358
AN - SCOPUS:85028741968
SN - 1471-2598
VL - 17
SP - 1265
EP - 1273
JO - Expert Opinion on Biological Therapy
JF - Expert Opinion on Biological Therapy
IS - 10
ER -