TY - JOUR
T1 - Fibrosis Regression After Eradication of Hepatitis C Virus
T2 - From Bench to Bedside
AU - Rockey, Don C.
AU - Friedman, Scott L.
N1 - Funding Information:
Conflicts of interest Don C. Rockey has no financial arrangements (eg, consultancies, stock ownership, equity interests, or patent-licensing arrangements) with a company whose product figures prominently in this manuscript or with a company making a competing product. His institution receives or has received research grant support within the last 12 months from the following: Intercept Pharmaceuticals, Galectin Therapeutics, Genfit, Gilead Sciences, Salix Pharmaceuticals, and Sequana Medical. Scott L. Friedman Scott L. Friedman has the following relationships: consulting for 89 Bio, Axcella, Blade, Bristol Myers Squibb, Can-Fite Biopharma, ChemomAb, Escient, Forbion, Galmed, Genevant, Gordian Biotechnology, Glycotest, Glympse Bio, Morphic Therapeutics, North Sea Therapeutics, Novartis, Ono Pharmaceuticals, Pfizer, Scholar Rock, and Surrozen; and stock or stock options from Blade Therapeutics, Escient, Galectin, Galmed, Genfit, Glympse, Intercept, Lifemax, Madrigal, Metacrine, Morphic Therapeutics, Nimbus, North Sea Therapeutics, Scholar Rock, and Surrozen.
Funding Information:
Funding This work was supported in part by the National Institutes of Health (R01 DK113159, P30 DK123704 to DCR, and R01 DK56621 to SLF).
Publisher Copyright:
© 2021 AGA Institute
PY - 2021/4
Y1 - 2021/4
N2 - Hepatitis C virus (HCV) infection and its complications have been the major cause of cirrhosis and its complications for several decades in the Western world. Until recently, treatment for HCV with interferon-based regimens was associated with moderate success but was difficult to tolerate. More recently, however, an arsenal of novel and highly effective direct-acting antiviral (DAA) drugs has transformed the landscape by curing HCV in a broad range of patients, including those with established advanced fibrosis, cirrhosis, comorbidities, and even those with complications of cirrhosis. Fibrosis is a dynamic process comprising both extracellular matrix deposition, as well as its degradation. With almost universal sustained virologic response (SVR) (ie, elimination of HCV), it is timely to explore whether HCV eradication can reverse fibrosis and cirrhosis. Indeed, fibrosis in several types of liver disease is reversible, including HCV. However, we do not know with certainty in whom fibrosis regression can be expected after HCV elimination, how quickly it occurs, and whether antifibrotic therapies will be indicated in those with persistent cirrhosis. This review summarizes the evidence for reversibility of fibrosis and cirrhosis after HCV eradication, its impact on clinical outcomes, and therapeutic prospects for directly promoting fibrosis regression in patients whose fibrosis persists after SVR.
AB - Hepatitis C virus (HCV) infection and its complications have been the major cause of cirrhosis and its complications for several decades in the Western world. Until recently, treatment for HCV with interferon-based regimens was associated with moderate success but was difficult to tolerate. More recently, however, an arsenal of novel and highly effective direct-acting antiviral (DAA) drugs has transformed the landscape by curing HCV in a broad range of patients, including those with established advanced fibrosis, cirrhosis, comorbidities, and even those with complications of cirrhosis. Fibrosis is a dynamic process comprising both extracellular matrix deposition, as well as its degradation. With almost universal sustained virologic response (SVR) (ie, elimination of HCV), it is timely to explore whether HCV eradication can reverse fibrosis and cirrhosis. Indeed, fibrosis in several types of liver disease is reversible, including HCV. However, we do not know with certainty in whom fibrosis regression can be expected after HCV elimination, how quickly it occurs, and whether antifibrotic therapies will be indicated in those with persistent cirrhosis. This review summarizes the evidence for reversibility of fibrosis and cirrhosis after HCV eradication, its impact on clinical outcomes, and therapeutic prospects for directly promoting fibrosis regression in patients whose fibrosis persists after SVR.
KW - Direct-Acting Antiviral
KW - Fibrosis Regression
KW - Hepatitis C Virus
KW - Sustained Virologic Response
UR - http://www.scopus.com/inward/record.url?scp=85103736543&partnerID=8YFLogxK
U2 - 10.1053/j.gastro.2020.09.065
DO - 10.1053/j.gastro.2020.09.065
M3 - Review article
C2 - 33529675
AN - SCOPUS:85103736543
SN - 0016-5085
VL - 160
SP - 1502-1520.e1
JO - Gastroenterology
JF - Gastroenterology
IS - 5
ER -