The remarkable history of the hepatitis C virus

被引:7
作者
Pol, Stanislas [1 ,2 ,3 ,4 ,5 ]
Lagaye, Sylvie [4 ,5 ]
机构
[1] Univ Paris 05, Paris, France
[2] Hop Cochin, AP HP, Dept Hepatol, Paris, France
[3] Inst Pasteur, INSERM UMS 20, Paris, France
[4] Inst Pasteur, Immunobiol Cellules Dendrit, Paris, France
[5] Inst Pasteur, INSERM U1223, 25 Rue Dr Roux, F-75015 Paris, France
关键词
HCV; Infection; Antiviral treatments; SUSTAINED VIROLOGICAL RESPONSE; PEGINTERFERON ALPHA-2B; GENETIC-VARIATION; VIRAL-HEPATITIS; RNA REPLICATION; CORE PROTEIN; LIFE-CYCLE; CDNA-CLONE; F-PROTEIN; T-CELLS;
D O I
10.1016/j.micinf.2019.06.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The infection with the hepatitis C virus (HCV) is an example of the translational research success. The reciprocal interactions between clinicians and scientists have allowed in 30 years the initiation of empirical treatments by interferon, the discovery of the virus, the development of serological and virological tools for diagnosis but also for prognosis (the non- invasive biochemical or morphological fibrosis tests, the predictors of the specific immune response including genetic IL28B polymorphisms). Finally, well-tolerated and effective treatments with oral antivirals inhibiting HCV non-structural viral proteins involved in viral replication have been marketed this last decade, allowing the cure of all infected subjects. HCV chronic infection, which is a public health issue, is a hepatic disease which may lead to a cirrhosis and an hepatocellular carcinoma (HCC) but also a systemic disease with extra-hepatic manifestations either associated with a cryoglobulinemic vasculitis or chronic inflammation. The HCV infection is the only chronic viral infection which may be cured: the so-called sustained virologic response, defined by undetectable HCV RNA 12 weeks after the end of the treatment, significantly reduces the risk of morbidity and mortality associated with hepatic and extra-hepatic manifestations which are mainly reversible. The history of HCV ends with the pangenotypic efficacy of the multiple combinations, easy to use for 8-12 weeks with one to three pills per day and little problems of tolerance. This explains the short 30 years from the virus discovery to the viral hepatitis elimination policy proposed by the World Health Organization (WHO) in 2016. (C) Springer Nature Limited 2019 reproduced with permission of SNCSC. Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:263 / 270
页数:8
相关论文
共 104 条
[1]   Regulatory T cells and viral liver disease [J].
Alatrakchi, Nadia ;
Koziel, Margaret .
JOURNAL OF VIRAL HEPATITIS, 2009, 16 (04) :223-229
[2]   In Vivo Dynamical Interactions between CD4 Tregs, CD8 Tregs and CD4+CD25- Cells in Mice [J].
Arazi, Arnon ;
Sharabi, Amir ;
Zinger, Heidy ;
Mozes, Edna ;
Neumann, Avidan U. .
PLOS ONE, 2009, 4 (12)
[3]   An overview of HCV molecular biology, replication and immune responses [J].
Ashfaq, Usman A. ;
Javed, Tariq ;
Rehman, Sidra ;
Nawaz, Zafar ;
Riazuddin, Sheikh .
VIROLOGY JOURNAL, 2011, 8
[4]   Assembly of infectious hepatitis C virus particles [J].
Bartenschlager, Ralf ;
Penin, Francois ;
Lohmann, Volker ;
Andre, Patrice .
TRENDS IN MICROBIOLOGY, 2011, 19 (02) :95-103
[5]   Cell entry of hepatitis C virus requires a set of co-receptors that include the CD81 tetraspanin and the SR-B1 scavenger receptor [J].
Bartosch, B ;
Vitelli, A ;
Granier, C ;
Goujon, C ;
Dubuisson, J ;
Pascale, S ;
Scarselli, E ;
Cortese, R ;
Nicosia, A ;
Cosset, FL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (43) :41624-41630
[6]   An algorithm for the grading of activity in chronic hepatitis C [J].
Bedossa, P ;
Poynard, T .
HEPATOLOGY, 1996, 24 (02) :289-293
[7]   Hepatitis C virus entry into the hepatocyte [J].
Belouzard, Sandrine ;
Cocquerel, Laurence ;
Dubuisson, Jean .
CENTRAL EUROPEAN JOURNAL OF BIOLOGY, 2011, 6 (06) :933-945
[8]   Global prevalence and genotype distribution of hepatitis C virus infection in 2015: a modelling study [J].
Blach, Sarah ;
Zeuzem, Stefan ;
Manns, Michael ;
Altraif, Ibrahim ;
Duberg, Ann-Sofi ;
Muljono, David H. ;
Waked, Imam ;
Alavian, Seyed M. ;
Lee, Mei-Hsuan ;
Negro, Francesco ;
Abaalkhail, Faisal ;
Abdou, Ahmed ;
Abdulla, Maheeba ;
Abou Rached, Antoine ;
Aho, Inka ;
Akarca, Ulus ;
Al Ghazzawi, Imad ;
Al Kaabi, Saad ;
Al Lawati, Faryal ;
Al Namaani, Khalid ;
Al Serkal, Youssif ;
Al-Busafi, Said A. ;
Al-Dabal, Layla ;
Aleman, Soo ;
Alghamdi, Abdullah S. ;
Aljumah, Abdulrahman A. ;
Al-Romaihi, Hamad E. ;
Andersson, Monique I. ;
Arendt, Vic ;
Arkkila, Perttu ;
Assiri, Abdullah M. ;
Baatarkhuu, Oidov ;
Bane, Abate ;
Ben-Ari, Ziv ;
Bergin, Colm ;
Bessone, Fernando ;
Bihl, Florian ;
Bizri, Abdul R. ;
Blachier, Martin ;
Blasco, Antonio J. ;
Mello, Carlos E. Brandao ;
Bruggmann, Philip ;
Brunton, Cheryl R. ;
Calinas, Filipe ;
Chan, Henry L. Y. ;
Chaudhry, Asad ;
Cheinquer, Hugo ;
Chen, Chien-Jen ;
Chien, Rong-Nan ;
Choi, Moon Seok .
LANCET GASTROENTEROLOGY & HEPATOLOGY, 2017, 2 (03) :161-176
[9]   Hepatitis C virus-like particle morphogenesis [J].
Blanchard, E ;
Brand, D ;
Trassard, S ;
Goudeau, A ;
Roingeard, P .
JOURNAL OF VIROLOGY, 2002, 76 (08) :4073-4079
[10]   Hepatitis C virus entry depends on clathrin-mediated endocytosis [J].
Blanchard, Emmanuelle ;
Belouzard, Sandrine ;
Goueslain, Lucie ;
Wakita, Takaji ;
Dubuisson, Jean ;
Wychowski, Czeslaw ;
Rouille, Yves .
JOURNAL OF VIROLOGY, 2006, 80 (14) :6964-6972