Critical challenges and emerging opportunities in hepatitis C virus research in an era of potent antiviral therapy: Considerations for scientists and funding agencies

被引:123
作者
Bartenschlager, Ralf [1 ,2 ,3 ,4 ]
Baumert, Thomas F. [5 ,6 ]
Bukh, Jens [7 ,8 ,9 ]
Houghton, Michael [10 ]
Lemon, Stanley M. [11 ,12 ]
Lindenbach, Brett D. [13 ]
Lohmann, Volker [1 ]
Moradpour, Darius [14 ]
Pietschmann, Thomas [3 ,4 ,15 ]
Rice, Charles M. [16 ]
Thimme, Robert [17 ]
Wakita, Takaji [18 ]
机构
[1] Heidelberg Univ, Dept Infect Dis, Mol Virol, Heidelberg, Germany
[2] German Canc Res Ctr, Div Virus Associated Carcinogenesis, Heidelberg, Germany
[3] German Ctr Infect Res DZIF, Partner Site Heidelberg, Heidelberg, Germany
[4] German Ctr Infect Res DZIF, Partner Site Hannover Braunschweig, Braunschweig, Germany
[5] INSERM, U1110, Inst Rech Malad Virales & Hepat, Strasbourg, France
[6] Univ Strasbourg, Strasbourg Inst Hosp Univ, Nouvel Hop Civil, Pole Hepatodigestif, Strasbourg, France
[7] Univ Copenhagen, Copenhagen Hepatitis C Program CO HEP, Dept Infect Dis, Copenhagen, Denmark
[8] Univ Copenhagen, Hvidovre Hosp, Clin Res Ctr, Copenhagen, Denmark
[9] Univ Copenhagen, Dept Immunol & Microbiol, Fac Hlth & Med Sci, Copenhagen, Denmark
[10] Univ Alberta, Li Ka Siting Inst Virol, Dept Med Microbiol & Immunol, Edmonton, AB, Canada
[11] Univ N Carolina, Lineberger Comprehens Canc Ctr, Dept Med, Chapel Hill, NC USA
[12] Univ N Carolina, Lineberger Comprehens Canc Ctr, Dept Microbiol & Immunol, Chapel Hill, NC USA
[13] Yale Univ, Sch Med, New Haven, CT USA
[14] Univ Lausanne, Ctr Hosp Univ Vaudois, Div Gastroenterol & Hepatol, Lausanne, Switzerland
[15] Ctr Expt & Clin Infect Res, TWINCORE, Inst Expt Virol, Hannover, Germany
[16] Rockefeller Univ, Ctr Study Hepatitis C, Lab Virol & Infect Dis, 1230 York Ave, New York, NY 10021 USA
[17] Univ Freiburg, Med Ctr, Dept Med 2, Ctr Med, Freiburg, Germany
[18] Natl Inst Infect Dis, Dept Virol 2, Tokyo, Japan
关键词
Direct acting antiviral therapy; HCV vaccine; Immune reconstitution; HCV research funding; SUSTAINED VIROLOGICAL RESPONSE; ADAPTIVE IMMUNE-RESPONSES; NON-B-HEPATITIS; CD8(+) T-CELLS; NEUTRALIZING ANTIBODIES; NON-A; HCV INFECTION; LIFE-CYCLE; MEMBRANOUS REPLICATION; STRUCTURAL BASIS;
D O I
10.1016/j.virusres.2018.02.016
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The development and clinical implementation of direct-acting antivirals (DAAs) has revolutionized the treatment of chronic hepatitis C. Infection with any hepatitis C virus (HCV) genotype can now be eliminated in more than 95% of patients with short courses of all-oral, well-tolerated drugs, even in those with advanced liver disease and liver transplant recipients. DAAs have proven so successful that some now consider HCV amenable to eradication, and continued research on the virus of little remaining medical relevance. However, given 400,000 HCV-related deaths annually important challenges remain, including identifying those who are infected, providing access to treatment and reducing its costs. Moreover, HCV infection rarely induces sterilizing immunity, and those who have been cured with DAAs remain at risk for reinfection. Thus, it is very unlikely that global eradication and elimination of the cancer risk associated with HCV infection can be achieved without a vaccine, yet research in that direction receives little attention. Further, over the past two decades HCV research has spearheaded numerous fundamental discoveries in the fields of molecular and cell biology, immunology and microbiology. It will continue to do so, given the unique opportunities afforded by the reagents and knowledge base that have been generated in the development and clinical application of DAAs. Considering these critical challenges and new opportunities, we conclude that funding for HCV research must be sustained.
引用
收藏
页码:53 / 62
页数:10
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