Peptides as Therapeutic Agents for Dengue Virus

被引:62
作者
Chew, Miaw-Fang [1 ]
Poh, Keat-Seong [2 ]
Poh, Chit-Laa [1 ]
机构
[1] Sunway Univ, Res Ctr Biomed Sci, 5 Jalan Univ, Bandar Sunway 47500, Selangor, Malaysia
[2] Univ Malaya, Dept Surg, Fac Med, Jalan Univ, Kuala Lumpur 50603, Malaysia
关键词
Dengue virus; Drug discovery; Peptides; Antiviral therapeutics; WEST-NILE-VIRUS; HUMAN DENDRITIC CELLS; PLACEBO-CONTROLLED TRIAL; ANTIBODY-DEPENDENT ENHANCEMENT; BORNE ENCEPHALITIS-VIRUS; TYPE-2 ENVELOPE PROTEIN; ORIGINAL ANTIGENIC SIN; YELLOW-FEVER VIRUS; DC-SIGN; DOMAIN-III;
D O I
10.7150/ijms.21875
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Dengue is an important global threat caused by dengue virus (DENV) that records an estimated 390 million infections annually. Despite the availability of CYD-TDV as a commercial vaccine, its long-term efficacy against all four dengue virus serotypes remains unsatisfactory. There is therefore an urgent need for the development of antiviral drugs for the treatment of dengue. Peptide was once a neglected choice of medical treatment but it has lately regained interest from the pharmaceutical industry following pioneering advancements in technology. In this review, the design of peptide drugs, antiviral activities and mechanisms of peptides and peptidomimetics (modified peptides) action against dengue virus are discussed. The development of peptides as inhibitors for viral entry, replication and translation is also described, with a focus on the three main targets, namely, the host cell receptors, viral structural proteins and viral non-structural proteins. The antiviral peptides designed based on these approaches may lead to the discovery of novel anti-DENV therapeutics that can treat dengue patients.
引用
收藏
页码:1342 / 1359
页数:18
相关论文
共 199 条
[1]   De novo synthesis of RNA by the dengue virus RNA-dependent RNA polymerase exhibits temperature dependence at the initiation but not elongation phase [J].
Ackermann, M ;
Padmanabhan, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (43) :39926-39937
[2]   Functional entry of dengue virus into Aedes albopictus mosquito cells is dependent on clathrinmediated endocytosis [J].
Acosta, Eliana G. ;
Castilla, Viviana ;
Damonte, Elsa B. .
JOURNAL OF GENERAL VIROLOGY, 2008, 89 :474-484
[3]   Alternative infectious entry pathways for dengue virus serotypes into mammalian cells [J].
Acosta, Eliana G. ;
Castilla, Viviana ;
Damonte, Elsa B. .
CELLULAR MICROBIOLOGY, 2009, 11 (10) :1533-1549
[4]   Broad Antiviral Activity of Carbohydrate-Binding Agents against the Four Serotypes of Dengue Virus in Monocyte-Derived Dendritic Cells [J].
Alen, Marijke M. F. ;
De Burghgraeve, Tine ;
Kaptein, Suzanne J. F. ;
Balzarini, Jan ;
Neyts, Johan ;
Schols, Dominique .
PLOS ONE, 2011, 6 (06)
[5]   Inhibition of Dengue Virus Entry into Target Cells Using Synthetic Antiviral Peptides [J].
Alhoot, Mohammed Abdelfatah ;
Rathinam, Alwin Kumar ;
Wang, Seok Mui ;
Manikam, Rishya ;
Sekaran, Shamala Devi .
INTERNATIONAL JOURNAL OF MEDICAL SCIENCES, 2013, 10 (06) :719-729
[6]   C-type lectins DC-SIGN and L-SIGN mediate cellular entry by Ebola virus in cis and in trans [J].
Alvarez, CP ;
Lasala, F ;
Carrillo, J ;
Muñiz, O ;
Corbí, AL ;
Delgado, R .
JOURNAL OF VIROLOGY, 2002, 76 (13) :6841-6844
[7]  
[Anonymous], 2016, DENG VACC WHO POS PA
[8]  
[Anonymous], 2017, Dengue Control
[9]   Identification and characterization of carbohydrate molecules in mammalian cells recognized by dengue virus type 2 [J].
Aoki, C ;
Hidari, KIPJ ;
Itonori, S ;
Yamada, A ;
Takahashi, N ;
Kasama, T ;
Hasebe, F ;
Islam, MA ;
Hatano, K ;
Matsuoka, K ;
Taki, T ;
Guo, CT ;
Takahashi, T ;
Sakano, Y ;
Suzuki, T ;
Miyamoto, D ;
Sugita, M ;
Terunuma, D ;
Morita, K ;
Suzuki, Y .
JOURNAL OF BIOCHEMISTRY, 2006, 139 (03) :607-614
[10]   Peptide entry inhibitors of enveloped viruses: The importance of interfacial hydrophobicity [J].
Badani, Hussain ;
Garry, Robert F. ;
Wimley, William C. .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2014, 1838 (09) :2180-2197