Hepatitis C Virus Glycan-Dependent Interactions and the Potential for Novel Preventative Strategies

被引:6
作者
LeBlanc, Emmanuelle V. [1 ]
Kim, Youjin [1 ]
Capicciotti, Chantelle J. [1 ,2 ,3 ]
Colpitts, Che C. [1 ]
机构
[1] Queens Univ, Dept Biomed & Mol Sci, Kingston, ON K7L 3N6, Canada
[2] Queens Univ, Dept Chem, Kingston, ON K7L 3N6, Canada
[3] Queens Univ, Dept Surg, Kingston, ON K7L 3N6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
hepatitis C virus; viral entry; glycans; vaccines; prophylaxis; N-LINKED GLYCANS; HCV ENVELOPE GLYCOPROTEINS; HYPERVARIABLE REGION 1; NEUTRALIZING ANTIBODIES; HEPARAN-SULFATE; E2; GLYCOPROTEIN; DC-SIGN; CELLULAR DETERMINANTS; URIDINE DERIVATIVES; MONOCLONAL-ANTIBODY;
D O I
10.3390/pathogens10060685
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Chronic hepatitis C virus (HCV) infections continue to be a major contributor to liver disease worldwide. HCV treatment has become highly effective, yet there are still no vaccines or prophylactic strategies available to prevent infection and allow effective management of the global HCV burden. Glycan-dependent interactions are crucial to many aspects of the highly complex HCV entry process, and also modulate immune evasion. This review provides an overview of the roles of viral and cellular glycans in HCV infection and highlights glycan-focused advances in the development of entry inhibitors and vaccines to effectively prevent HCV infection.
引用
收藏
页数:19
相关论文
共 144 条
[1]   Additional Glycosylation Within a Specific Hypervariable Region of Subtype 3a of Hepatitis C Virus Protects Against Virus Neutralization [J].
Anjum, Sadia ;
Wahid, Ahmed ;
Afzal, Muhammad Sohail ;
Albecka, Anna ;
Alsaleh, Khaled ;
Ahmad, Tahir ;
Baumert, Thomas F. ;
Wychowski, Czeslaw ;
Qadri, Ishtiaq ;
Penin, Francois ;
Dubuisson, Jean .
JOURNAL OF INFECTIOUS DISEASES, 2013, 208 (11) :1888-1897
[2]   The past, present and future of neutralizing antibodies for hepatitis C virus [J].
Ball, Jonathan K. ;
Tarr, Alexander W. ;
McKeating, Jane A. .
ANTIVIRAL RESEARCH, 2014, 105 :100-111
[3]   Cellular binding of hepatitis C virus envelope glycoprotein E2 requires cell surface heparan sulfate [J].
Barth, H ;
Schäfer, C ;
Adah, MI ;
Zhang, FM ;
Linhardt, RJ ;
Toyoda, H ;
Kinoshita-Toyoda, A ;
Toida, T ;
van Kuppevelt, TH ;
Depla, E ;
von Weizsäcker, F ;
Blum, HE ;
Baumert, TF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (42) :41003-41012
[4]   Viral and cellular determinants of the hepatitis C virus envelope-heparan sulfate interaction [J].
Barth, Heidi ;
Schnober, Eva K. ;
Zhang, Fuming ;
Linhardt, Robert J. ;
Depla, Erik ;
Boson, Bertrand ;
Cosset, Francois-Loic ;
Patel, Arvind H. ;
Blum, Hubert E. ;
Baumert, Thomas F. .
JOURNAL OF VIROLOGY, 2006, 80 (21) :10579-10590
[5]   Infectious hepatitis C virus pseudo-particles containing functional E1-E2 envelope protein complexes [J].
Bartosch, B ;
Dubuisson, J ;
Cosset, FL .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (05) :633-642
[6]  
Bastida Inaki, 2020, Drug Discov Today Technol, V35-36, P45, DOI 10.1016/j.ddtec.2020.09.004
[7]   Sulfated homologues of heparin inhibit hepatitis C virus entry into mammalian cells [J].
Basu, Arnab ;
Kanda, Tatsuo ;
Beyene, Aster ;
Saito, Kousuke ;
Meyer, Keith ;
Ray, Ranjit .
JOURNAL OF VIROLOGY, 2007, 81 (08) :3933-3941
[8]   A prophylactic hepatitis C virus vaccine: A distant peak still worth climbing [J].
Baumert, Thomas F. ;
Fauvelle, Catherine ;
Chen, Diana Y. ;
Lauer, Georg M. .
JOURNAL OF HEPATOLOGY, 2014, 61 :S34-S44
[9]   Influence of N-linked glycans on intracellular transport of hepatitis C virus E1 chimeric glycoprotein and its role in pseudotype virus infectivity [J].
Beyene, A ;
Basu, A ;
Meyer, K ;
Ray, R .
VIROLOGY, 2004, 324 (02) :273-285
[10]   Structure-activity studies of (-)-epigallocatechin gallate derivatives as HCV entry inhibitors [J].
Bhat, Rohit ;
Adam, Amna T. ;
Lee, Jungeun Jasmine ;
Deloison, Gaspard ;
Rouille, Yves ;
Seron, Karin ;
Rotella, David P. .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2014, 24 (17) :4162-4165