Semin Liver Dis 2011; 31(4): 410-419
DOI: 10.1055/s-0031-1297929
© Thieme Medical Publishers

The Conundrum of Relapse in STAT-C Therapy: Does HCV Play the Red Queen or Rip Van Winkle?

Robert Ralston1 , 3 , Ira Jacobson2 , Margaret Scull1
  • 1Laboratory of Virology and Infectious Disease and Center for the Study of Hepatitis C, The Rockefeller University, New York, New York
  • 2Department of Medicine, Division of Gastroenterology and Hepatology, Center for the Study of Hepatitis C, Weill Medical College, New York, New York
  • 3Current address: Department of Molecular Microbiology and Immunology, School of Medicine, University of Missouri, Columbia, Missouri
Further Information

Publication History

Publication Date:
21 December 2011 (online)

ABSTRACT

New treatments for chronic hepatitis C combining direct-acting antivirals (DAAs) with pegylated interferon and ribavirin (PEG-IFN/RBV) have dramatically increased the number of patients whose viral load declines to undetectable levels early in treatment. Most go on to achieve a sustained virologic response, but some patients who maintain undetectable levels of virus throughout treatment later relapse during follow-up. These data suggest that hepatitis C virus (HCV) genomes may persist in form(s) that are refractory to eradication by DAAs and PEG-IFN/RBV. Here we examine the molecular biology of HCV replication and review the clinical virology of relapse for clues as to how the virus might survive months of antiviral therapy to later reappear when treatment is withdrawn.

REFERENCES

  • 1 Poordad F, McCone Jr J, Bacon B R SPRINT-2 Investigators et al. Boceprevir for untreated chronic HCV genotype 1 infection.  N Engl J Med. 2011;  364 (13) 1195-1206
  • 2 Bacon B R, Gordon S C, Lawitz E HCV RESPOND-2 Investigators et al. Boceprevir for previously treated chronic HCV genotype 1 infection.  N Engl J Med. 2011;  364 (13) 1207-1217
  • 3 Jacobson I M, McHutchison J G, Dusheiko G ADVANCE Study Team et al. Telaprevir for previously untreated chronic hepatitis C virus infection.  N Engl J Med. 2011;  364 (25) 2405-2416
  • 4 Zeuzem S, Andreone P, Pol S REALIZE Study Team et al. Telaprevir for retreatment of HCV infection.  N Engl J Med. 2011;  364 (25) 2417-2428
  • 5 Pawlotsky J M, Cocquerel L, Durantel D et al.. HCV research 20 years after discovery: a summary of the 16th international symposium on hepatitis C virus and related viruses.  Gastroenterology. 2010;  138 (1) 6-12, e1–e2
  • 6 Lange C M, Sarrazin C, Zeuzem S. Review article: specifically targeted anti-viral therapy for hepatitis C - a new era in therapy.  Aliment Pharmacol Ther. 2010;  32 (1) 14-28
  • 7 Forestier N, Larrey D, Guyader D et al.. Treatment of chronic hepatitis C patients with the NS3/4A protease inhibitor danoprevir (ITMN-191/RG7227) leads to robust reductions in viral RNA: a phase 1b multiple ascending dose study.  J Hepatol. 2011;  54 (6) 1130-1136
  • 8 Reesink H W, Fanning G C, Farha K A et al.. Rapid HCV-RNA decline with once daily TMC435: a phase I study in healthy volunteers and hepatitis C patients.  Gastroenterology. 2010;  138 (3) 913-921
  • 9 McHutchison J G, Lawitz E J, Shiffman M L IDEAL Study Team et al. Peginterferon alfa-2b or alfa-2a with ribavirin for treatment of hepatitis C infection.  N Engl J Med. 2009;  361 (6) 580-593
  • 10 U.S. Food and Drug Administration. US FDA Antiviral Drugs Advisory Committee Briefing Document: Background Material for Boceprevir. Silver Spring, MD: U.S. Food and Drug Administration; 2011: 31
  • 11 U.S. Food and Drug Administration. US FDA Antiviral Drugs Advisory Committee Briefing Document for NDA 201–917 Telaprevir 375 mg Tablets. Silver Spring, MD: U.S. Food and Drug Administration; 2011: 22
  • 12 U.S. Food and Drug Administration. US FDA Antiviral Drugs Advisory Committee Briefing Document: Boceprevir Capsules (NDA 202–258) Briefing Document. Whitehouse Station, NJ: Merck and Co; 2011: 90
  • 13 U.S. Food and Drug Administration. US FDA Antiviral Drugs Advisory Committee Briefing Document: Telaprevir 375-mg Film-Coated Tablet for the Treatment of Genotype 1 Chronic Hepatitis C. Cambridge, MA: Vertex Pharmaceuticals; 2011: 147
  • 14 Ludmerer S W, Graham D J, Boots E et al.. Replication fitness and NS5B drug sensitivity of diverse hepatitis C virus isolates characterized by using a transient replication assay.  Antimicrob Agents Chemother. 2005;  49 (5) 2059-2069
  • 15 Le Pogam S, Seshaadri A, Kosaka A et al.. Existence of hepatitis C virus NS5B variants naturally resistant to non-nucleoside, but not to nucleoside, polymerase inhibitors among untreated patients.  J Antimicrob Chemother. 2008;  61 (6) 1205-1216
  • 16 Pockros P, Jensen D, Tsai N et al.. First SVR data with the nucleoside analogue polymerase inhibitor mericitabine (RG7128) combined with peginterferon/ribavirin in treatment-naive HCV G1/4 patients: interim analysis from the JUMP-C trial. Paper presented at: European Association for the Study of the Liver 46th Annual Meeting March 30–April 3, 2011. Berlin, Germany;
  • 17 van Valen L. A new evolutionary law.  Evol Theory. 1973;  1 1-30
  • 18 Domingo E, Escarmís C, Sevilla N et al.. Basic concepts in RNA virus evolution.  FASEB J. 1996;  10 (8) 859-864
  • 19 Pham T N, Michalak T I. Occult persistence and lymphotropism of hepatitis C viral infection.  World J Gastroenterol. 2008;  14 (18) 2789-2793
  • 20 Sumpter Jr R, Loo Y M, Foy E et al.. Regulating intracellular antiviral defense and permissiveness to hepatitis C virus RNA replication through a cellular RNA helicase, RIG-I.  J Virol. 2005;  79 (5) 2689-2699
  • 21 Shoukry N H, Cawthon A G, Walker C M. Cell-mediated immunity and the outcome of hepatitis C virus infection.  Annu Rev Microbiol. 2004;  58 391-424
  • 22 Tillmann H L, Thompson A J, Patel K German Anti-D Study Group et al. A polymorphism near IL28B is associated with spontaneous clearance of acute hepatitis C virus and jaundice.  Gastroenterology. 2010;  139 (5) 1586-1592, 1592, e1
  • 23 Walters K A, Katze M G. Using high-throughput genomics to study hepatitis C: what determines the outcome of infection?.  Antiviral Res. 2009;  81 (3) 198-208
  • 24 Sugano M, Hayashi Y, Yoon S et al.. Quantitation of hepatitis C viral RNA in liver and serum samples using competitive polymerase chain reaction.  J Clin Pathol. 1995;  48 (9) 820-825
  • 25 Neumann A U, Lam N P, Dahari H et al.. Hepatitis C viral dynamics in vivo and the antiviral efficacy of interferon-alpha therapy.  Science. 1998;  282 (5386) 103-107
  • 26 Guedj J, Dahari H, Rong L et al.. New insights into the mechanism of action of interferon-alpha and BMS-790052: a multi-scale mathematical modeling approach. Paper presented at: 18th International Symposium on Hepatitis C Virus and Related Viruses September 8–12, 2011. Seattle, WA;
  • 27 Gowans EJ. Distribution of markers of hepatitis C virus infection throughout the body.  Semin Liver Dis. 2001;  20 (1) 85-102
  • 28 Idrees M, Lal A, Malik F A et al.. Occult hepatitis C virus infection and associated predictive factors: the Pakistan experience.  Infect Genet Evol. 2011;  11 (2) 442-445
  • 29 Carreño V, Pardo M, López-Alcorocho J M, Rodríguez-Iñigo E, Bartolomé J, Castillo I. Detection of hepatitis C virus (HCV) RNA in the liver of healthy, anti-HCV antibody-positive, serum HCV RNA-negative patients with normal alanine aminotransferase levels.  J Infect Dis. 2006;  194 (1) 53-60
  • 30 Castillo I, Rodríguez-Iñigo E, López-Alcorocho J M, Pardo M, Bartolomé J, Carreño V. Hepatitis C virus replicates in the liver of patients who have a sustained response to antiviral treatment.  Clin Infect Dis. 2006;  43 (10) 1277-1283
  • 31 Carreño V. Occult hepatitis C virus infection: a new form of hepatitis C.  World J Gastroenterol. 2006;  12 (43) 6922-6925
  • 32 Chang M, Williams O, Mittler J et al.. Dynamics of hepatitis C virus replication in human liver.  Am J Pathol. 2003;  163 (2) 433-444
  • 33 Egger D, Wölk B, Gosert R et al.. Expression of hepatitis C virus proteins induces distinct membrane alterations including a candidate viral replication complex.  J Virol. 2002;  76 (12) 5974-5984
  • 34 Moradpour D, Penin F, Rice C M. Replication of hepatitis C virus.  Nat Rev Microbiol. 2007;  5 (6) 453-463
  • 35 Gosert R, Egger D, Lohmann V et al.. Identification of the hepatitis C virus RNA replication complex in Huh-7 cells harboring subgenomic replicons.  J Virol. 2003;  77 (9) 5487-5492
  • 36 Rouillé Y, Helle F, Delgrange D et al.. Subcellular localization of hepatitis C virus structural proteins in a cell culture system that efficiently replicates the virus.  J Virol. 2006;  80 (6) 2832-2841
  • 37 Pfeifer U, Thomssen R, Legler K et al.. Experimental non-A, non-B hepatitis: four types of cytoplasmic alteration in hepatocytes of infected chimpanzees.  Virchows Arch B Cell Pathol Incl Mol Pathol. 1980;  33 (3) 233-243
  • 38 Schaff Z, Tabor E, Jackson D R, Gerety R J. Ultrastructural alterations in serial liver biopsy specimens from chimpanzees experimentally infected with a human non-A, non-B hepatitis agent.  Virchows Arch B Cell Pathol Incl Mol Pathol. 1984;  45 (3) 301-312
  • 39 De Vos R, Verslype C, Depla E et al.. Ultrastructural visualization of hepatitis C virus components in human and primate liver biopsies.  J Hepatol. 2002;  37 (3) 370-379
  • 40 Kasprzak A, Seidel J, Biczysko W, Wysocki J, Spachacz R, Zabel M. Intracellular localization of NS3 and C proteins in chronic hepatitis C.  Liver Int. 2005;  25 (4) 896-903
  • 41 Falcón V, Acosta-Rivero N, Chinea G et al.. Ultrastructural evidences of HCV infection in hepatocytes of chronically HCV-infected patients.  Biochem Biophys Res Commun. 2003;  305 (4) 1085-1090
  • 42 Asselah T, Bièche I, Mansouri A et al.. In vivo hepatic endoplasmic reticulum stress in patients with chronic hepatitis C.  J Pathol. 2010;  221 (3) 264-274
  • 43 Ferraris P, Blanchard E, Roingeard P. Ultrastructural and biochemical analyses of hepatitis C virus-associated host cell membranes.  J Gen Virol. 2010;  91 (Pt 9) 2230-2237
  • 44 Reiss S, Rebhan I, Backes P et al.. Recruitment and activation of a lipid kinase by hepatitis C virus NS5A is essential for integrity of the membranous replication compartment.  Cell Host Microbe. 2011;  9 (1) 32-45
  • 45 Knoops K, Kikkert M, Worm S H et al.. SARS-coronavirus replication is supported by a reticulovesicular network of modified endoplasmic reticulum.  PLoS Biol. 2008;  6 (9) e226
  • 46 Uchil P D, Satchidanandam V. Architecture of the flaviviral replication complex. Protease, nuclease, and detergents reveal encasement within double-layered membrane compartments.  J Biol Chem. 2003;  278 (27) 24388-24398
  • 47 Mackenzie J M, Jones M K, Young P R. Immunolocalization of the dengue virus nonstructural glycoprotein NS1 suggests a role in viral RNA replication.  Virology. 1996;  220 (1) 232-240
  • 48 Westaway E G, Mackenzie J M, Kenney M T, Jones M K, Khromykh A A. Ultrastructure of Kunjin virus-infected cells: colocalization of NS1 and NS3 with double-stranded RNA, and of NS2B with NS3, in virus-induced membrane structures.  J Virol. 1997;  71 (9) 6650-6661
  • 49 Quinkert D, Bartenschlager R, Lohmann V. Quantitative analysis of the hepatitis C virus replication complex.  J Virol. 2005;  79 (21) 13594-13605
  • 50 Syed G H, Amako Y, Siddiqui A. Hepatitis C virus hijacks host lipid metabolism.  Trends Endocrinol Metab. 2010;  21 (1) 33-40
  • 51 Gastaminza P, Cheng G, Wieland S, Zhong J, Liao W, Chisari F V. Cellular determinants of hepatitis C virus assembly, maturation, degradation, and secretion.  J Virol. 2008;  82 (5) 2120-2129
  • 52 Russell R S, Meunier J C, Takikawa S et al.. Advantages of a single-cycle production assay to study cell culture-adaptive mutations of hepatitis C virus.  Proc Natl Acad Sci U S A. 2008;  105 (11) 4370-4375
  • 53 Brimacombe C L, Grove J, Meredith L W et al.. Neutralizing antibody-resistant hepatitis C virus cell-to-cell transmission.  J Virol. 2011;  85 (1) 596-605
  • 54 Valli M B, Serafino A, Crema A et al.. Transmission in vitro of hepatitis C virus from persistently infected human B-cells to hepatoma cells by cell-to-cell contact.  J Med Virol. 2006;  78 (2) 192-201
  • 55 Timpe J M, Stamataki Z, Jennings A et al.. Hepatitis C virus cell-cell transmission in hepatoma cells in the presence of neutralizing antibodies.  Hepatology. 2008;  47 (1) 17-24
  • 56 Witteveldt J, Evans M J, Bitzegeio J et al.. CD81 is dispensable for hepatitis C virus cell-to-cell transmission in hepatoma cells.  J Gen Virol. 2009;  90 (Pt 1) 48-58
  • 57 Catanese M T, Loureiro J, Jones C T et al.. Viral and cellular determinants of HCV cell-to-cell spread. Paper presented at: 18th International Symposium on Hepatitis C Virus and Related Viruses September 8–12, 2011. Seattle, WA;
  • 58 Sigal A, Kim J T, Balazs A B et al.. Cell-to-cell spread of HIV permits ongoing replication despite antiretroviral therapy.  Nature. 2011;  477 (7362) 95-98
  • 59 Hu Y, Shahidi A, Park S, Guilfoyle D, Hirshfield I. Detection of extrahepatic hepatitis C virus replication by a novel, highly sensitive, single-tube nested polymerase chain reaction.  Am J Clin Pathol. 2003;  119 (1) 95-100
  • 60 Sung V M, Shimodaira S, Doughty A L et al.. Establishment of B-cell lymphoma cell lines persistently infected with hepatitis C virus in vivo and in vitro: the apoptotic effects of virus infection.  J Virol. 2003;  77 (3) 2134-2146
  • 61 Steffan A, Marianneau P, Caussin-Schwemling C et al.. Ultrastructural observations in hepatitis C virus-infected lymphoid cells.  Microbes Infect. 2001;  3 (3) 193-202
  • 62 Pham T N, Michalak T I. Occult persistence and lymphotropism of hepatitis C virus infection.  World J Gastroenterol. 2008;  14 (18) 2789-2793
  • 63 Zehender G, Meroni L, De Maddalena C, Varchetta S, Monti G, Galli M. Detection of hepatitis C virus RNA in CD19 peripheral blood mononuclear cells of chronically infected patients.  J Infect Dis. 1997;  176 (5) 1209-1214
  • 64 Boisvert J, He X S, Cheung R, Keeffe E B, Wright T, Greenberg H B. Quantitative analysis of hepatitis C virus in peripheral blood and liver: replication detected only in liver.  J Infect Dis. 2001;  184 (7) 827-835
  • 65 Laporte J, Bain C, Maurel P, Inchauspe G, Agut H, Cahour A. Differential distribution and internal translation efficiency of hepatitis C virus quasispecies present in dendritic and liver cells.  Blood. 2003;  101 (1) 52-57
  • 66 Sansonno D, Tucci F A, Lauletta G et al.. Hepatitis C virus productive infection in mononuclear cells from patients with cryoglobulinaemia.  Clin Exp Immunol. 2007;  147 (2) 241-248
  • 67 Laskus T, Radkowski M, Jablonska J et al.. Human immunodeficiency virus facilitates infection/replication of hepatitis C virus in native human macrophages.  Blood. 2004;  103 (10) 3854-3859
  • 68 Lerat H, Rumin S, Habersetzer F et al.. In vivo tropism of hepatitis C virus genomic sequences in hematopoietic cells: influence of viral load, viral genotype, and cell phenotype.  Blood. 1998;  91 (10) 3841-3849
  • 69 Di Liberto G, Roque-Afonso A M, Kara R et al.. Clinical and therapeutic implications of hepatitis C virus compartmentalization.  Gastroenterology. 2006;  131 (1) 76-84
  • 70 Pham T N, Mulrooney-Cousins P M, Mercer S E et al.. Antagonistic expression of hepatitis C virus and alpha interferon in lymphoid cells during persistent occult infection.  J Viral Hepat. 2007;  14 (8) 537-548
  • 71 Radkowski M, Gallegos-Orozco J F, Jablonska J et al.. Persistence of hepatitis C virus in patients successfully treated for chronic hepatitis C.  Hepatology. 2005;  41 (1) 106-114
  • 72 Pham T N, MacParland S A, Mulrooney P M et al.. Hepatitis C virus persistence after spontaneous or treatment-induced resolution of hepatitis C.  J Virol. 2004;  78 (11) 5867-5874
  • 73 Natarajan V, Kottilil S, Hazen A et al.. HCV in peripheral blood mononuclear cells are predominantly carried on the surface of cells in HIV/HCV co-infected individuals.  J Med Virol. 2010;  82 (12) 2032-2037
  • 74 Ramirez S, Perez-Del-Pulgar S, Carrion J A et al.. Hepatitis C virus compartmentalization and infection recurrence after liver transplantation.  Am J Transplant. 2009;  9 (7) 1591-1601
  • 75 Maggi F, Fornai C, Vatteroni M L et al.. Differences in hepatitis C virus quasispecies composition between liver, peripheral blood mononuclear cells and plasma.  J Gen Virol. 1997;  78 (Pt 7) 1521-1525
  • 76 Revie D, Salahuddin S Z. Human cell types important for hepatitis C virus replication in vivo and in vitro: old assertions and current evidence.  Virol J. 2011;  8 346
  • 77 Martínez J L, Rojo F. Metabolic regulation of antibiotic resistance.  FEMS Microbiol Rev. 2011;  35 (5) 768-789
  • 78 Klepper A, Eng F, Walewski J et al.. Contrary to published models of HCV RNA replication, heat denaturation reveals that much of the HCV in natural infections is in double-stranded form. Paper presented at: 18th International Symposium on Hepatitis C Virus and Related Viruses September 8–12, 2011. Seattle, WA;
  • 79 Jones C T, Murray C L, Eastman D K, Tassello J, Rice C M. Hepatitis C virus p7 and NS2 proteins are essential for production of infectious virus.  J Virol. 2007;  81 (16) 8374-8383
  • 80 Pedersen I M, Cheng G, Wieland S et al.. Interferon modulation of cellular microRNAs as an antiviral mechanism.  Nature. 2007;  449 (7164) 919-922
  • 81 Chang J, Guo J T, Jiang D, Guo H, Taylor J M, Block T M. Liver-specific microRNA miR-122 enhances the replication of hepatitis C virus in nonhepatic cells.  J Virol. 2008;  82 (16) 8215-8223
  • 82 Jopling C L. Regulation of hepatitis C virus by microRNA-122.  Biochem Soc Trans. 2008;  36 (Pt 6) 1220-1223
  • 83 Randall G, Panis M, Cooper J D et al.. Cellular cofactors affecting hepatitis C virus infection and replication.  Proc Natl Acad Sci U S A. 2007;  104 (31) 12884-12889
  • 84 Henke J I, Goergen D, Zheng J et al.. microRNA-122 stimulates translation of hepatitis C virus RNA.  EMBO J. 2008;  27 (24) 3300-3310
  • 85 Jangra R K, Yi M, Lemon S M. Regulation of hepatitis C virus translation and infectious virus production by the microRNA miR-122.  J Virol. 2010;  84 (13) 6615-6625
  • 86 Roberts A P, Lewis A P, Jopling C L. miR-122 activates hepatitis C virus translation by a specialized mechanism requiring particular RNA components.  Nucleic Acids Res. 2011;  39 (17) 7716-7729
  • 87 Sagan S, Sarnow P. Stabilization of the HCV RNA genome by miR-122. Paper presented at: 18th International Symposium on Hepatitis C Virus and Related Viruses September 8–12, 2011. Seattle, WA;
  • 88 Shimakami T, Yamane D, Jangra R K et al.. miR-122 stabilizes hepatitis C virus RNA by an Ago2-dependent mechanism. Paper presented at: 18th International Symposium on Hepatitis C Virus and Related Viruses September 8–12, 2011. Seattle, WA;
  • 89 Negro F. Mechanisms of hepatitis C virus-related insulin resistance.  Clin Res Hepatol Gastroenterol. 2011;  35 (5) 358-363
  • 90 Rasmussen A L, Diamond D L, McDermott J E et al.. Systems virology identifies a mitochondrial Fatty Acid oxidation enzyme, dodecenoyl coenzyme a delta isomerase, required for hepatitis C virus replication and likely pathogenesis.  J Virol. 2011;  85 (22) 11646-11654
  • 91 Diamond D L, Syder A J, Jacobs J M et al.. Temporal proteome and lipidome profiles reveal hepatitis C virus-associated reprogramming of hepatocellular metabolism and bioenergetics.  PLoS Pathog. 2010;  6 (1) e1000719
  • 92 Berger K L, Randall G. Potential roles for cellular cofactors in hepatitis C virus replication complex formation.  Commun Integr Biol. 2009;  2 (6) 471-473
  • 93 Estrabaud E, De Muynck S, Asselah T. Activation of unfolded protein response and autophagy during HCV infection modulates innate immune response.  J Hepatol. 2011;  55 (5) 1150-1153
  • 94 Ke P Y, Chen S S. Autophagy: a novel guardian of HCV against innate immune response.  Autophagy. 2011;  7 (5) 533-535
  • 95 Ke P Y, Chen S S. Activation of the unfolded protein response and autophagy after hepatitis C virus infection suppresses innate antiviral immunity in vitro.  J Clin Invest. 2011;  121 (1) 37-56
  • 96 Zeuzem S, Poordad F, Gordon S C et al.. Boceprevir resistance-associated variants (RAVs) are observed more frequently in HCV (GT1)-infected patients with poor response to peginterferon alfa-2b/ribavirin. Paper presented at: European Association for the Study of the Liver 46th Annual Meeting March 30–April 3, 2011. Berlin, Germany;
  • 97 Jiang M, Vijgen L, Sullivan J et al.. Phenotypic characterization of HCV NS3 protease from patient isolates in phase 2 clinical trials of telaprevir. Paper presented at: 18th International Symposium on Hepatitis C Virus and Related Viruses September 8–12, 2011. Seattle, WA;
  • 98 Shimakami T, Welsch C, Yamane D et al.. Protease inhibitor-resistant hepatitis C virus mutants with reduced fitness from impaired production of infectious virus.  Gastroenterology. 2011;  140 (2) 667-675
  • 99 Kieffer T L, Sarrazin C, Miller J S et al.. Telaprevir and pegylated interferon-alpha-2a inhibit wild-type and resistant genotype 1 hepatitis C virus replication in patients.  Hepatology. 2007;  46 (3) 631-639
  • 100 Le Pogam S, Seshaadri A, Ewing A et al.. RG7128 alone or in combination with pegylated interferon-α2a and ribavirin prevents hepatitis C virus (HCV) Replication and selection of resistant variants in HCV-infected patients.  J Infect Dis. 2010;  202 (10) 1510-1519
  • 101 Lawitz E, Nguyen T, Younes Z et al.. Valopicitabine NM283 plus PEGinterferon in treatment-naive hepatitis C patients with HCV genotype 1 infection: HCV RNA clearance during 24 weeks of treatment.  Hepatology. 2007;  44 223A
  • 102 Ali S, Leveque V, Le Pogam S et al.. Selected replicon variants with low-level in vitro resistance to the hepatitis C virus NS5B polymerase inhibitor PSI-6130 lack cross-resistance with R1479.  Antimicrob Agents Chemother. 2008;  52 (12) 4356-4369
  • 103 Fridell R A, Qiu D, Valera L, Wang C, Rose R E, Gao M. Distinct functions of NS5A in hepatitis C virus RNA replication uncovered by studies with the NS5A inhibitor BMS-790052.  J Virol. 2011;  85 (14) 7312-7320
  • 104 Lok A, Gardiner D, Lawitz E et al.. Quadruple therapy with BMS-790052, BMS-650032 and PEG-IFN/RBV for 24 weeks results in 100% SVR12 in HCV genotype 1 null responders (Abstract 1356).  J Hepatol. 2011;  54 S536
  • 105 Fried M W, Hadziyannis S J, Shiffman M L, Messinger D, Zeuzem S. Rapid virological response is the most important predictor of sustained virological response across genotypes in patients with chronic hepatitis C virus infection.  J Hepatol. 2011;  55 (1) 69-75
  • 106 Guedj J, Bazzoli C, Neumann A U, Mentré F. Design evaluation and optimization for models of hepatitis C viral dynamics.  Stat Med. 2011;  30 (10) 1045-1056
  • 107 Guedj J, Dahari H, Shudo E, Smith S, Perelson A. Hepatitis C viral kinetics with the nucleoside polymerase inhibitor RG7128. Paper presented at: 18th International Symposium on Hepatitis C Virus and Related Viruses September 8–12, 2011. Seattle, WA;
  • 108 Pearson J E, Krapivsky P, Perelson A S. Stochastic theory of early viral infection: continuous versus burst production of virions.  PLOS Comput Biol. 2011;  7 (2) e1001058
  • 109 Zeuzem S, Schmidt J M, Lee J H, von Wagner M, Teuber G, Roth W K. Hepatitis C virus dynamics in vivo: effect of ribavirin and interferon alfa on viral turnover.  Hepatology. 1998;  28 (1) 245-252
  • 110 Zeuzem S, Lee J H, Franke A et al.. Quantification of the initial decline of serum hepatitis C virus RNA and response to interferon alfa.  Hepatology. 1998;  27 (4) 1149-1156
  • 111 Dusheiko G, Main J, Thomas H et al.. Ribavirin treatment for patients with chronic hepatitis C: results of a placebo-controlled study.  J Hepatol. 1996;  25 (5) 591-598
  • 112 Pawlotsky J M, Dahari H, Neumann A U et al.. Antiviral action of ribavirin in chronic hepatitis C.  Gastroenterology. 2004;  126 (3) 703-714
  • 113 Fried M W, Shiffman M L, Reddy K R et al.. Peginterferon alfa-2a plus ribavirin for chronic hepatitis C virus infection.  N Engl J Med. 2002;  347 (13) 975-982
  • 114 Manns M P, McHutchison J G, Gordon S C et al.. Peginterferon alfa-2b plus ribavirin compared with interferon alfa-2b plus ribavirin for initial treatment of chronic hepatitis C: a randomised trial.  Lancet. 2001;  358 (9286) 958-965
  • 115 Hézode C, Forestier N, Dusheiko G PROVE2 Study Team et al. Telaprevir and peginterferon with or without ribavirin for chronic HCV infection.  N Engl J Med. 2009;  360 (18) 1839-1850
  • 116 McHutchison J G, Everson G T, Gordon S C PROVE1 Study Team et al. Telaprevir with peginterferon and ribavirin for chronic HCV genotype 1 infection.  N Engl J Med. 2009;  360 (18) 1827-1838

Robert RalstonPh.D. 

Department of Molecular Microbiology and Immunology, School of Medicine, University of Missouri

1201 E. Rollins Drive, Columbia, MO 65211

Email: ralstonr@missouri.edu