Glycodendritic structures: promising new antiviral drugs

被引:60
作者
Rojo, J
Delgado, R
机构
[1] CSIC, Inst Invest Quim, Grp Carbohidratos, Seville 41092, Spain
[2] Hosp Univ 12 Octubre, Mol Microbiol Lab, Microbiol Serv, Madrid, Spain
关键词
boltorn; DC-SIGN; dendrimers; Ebola virus;
D O I
10.1093/jac/dkh399
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
DC-SIGN, a C-type lectin expressed by dendritic cells, is able to recognize high mannosylated glycoproteins at the surface of a broad range of pathogens including viruses, bacteria, fungi and parasites. For at least some of these agents this interaction appears to be an important part of the infection process. Therefore, this lectin might be considered in the design of new antiviral drugs. In this manner, multivalent carbohydrate systems based on dendrimers and dendritic polymers are promising candidates as antiviral drugs. Boltorn hyperbranched dendritic polymers functionalized with mannose have been used to inhibit DC-SIGN-mediated infection in an Ebola-pseudotyped viral model. Their physiological solubility, lack of toxicity and especially their low price suggest the application of these glycodendritic polymers for possible formulation as microbicides.
引用
收藏
页码:579 / 581
页数:3
相关论文
共 20 条
[1]   Glycodendritic structures based on Boltorn hyperbranched polymers and their interactions with Lens culinaris lectin [J].
Arce, E ;
Nieto, PM ;
Díaz, V ;
Castro, RG ;
Bernad, A ;
Rojo, J .
BIOCONJUGATE CHEMISTRY, 2003, 14 (04) :817-823
[2]   Dendritic cells and the control of immunity [J].
Banchereau, J ;
Steinman, RM .
NATURE, 1998, 392 (6673) :245-252
[3]   Evaluations of unformulated and formulated dendrimer-based microbicide candidates in mouse and guinea pig models of genital herpes [J].
Bernstein, DI ;
Stanberry, LR ;
Sacks, S ;
Ayisi, NK ;
Gong, YH ;
Ireland, J ;
Mumper, RJ ;
Holan, G ;
Matthews, B ;
McCarthy, T ;
Bournel, N .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (12) :3784-3788
[4]  
Bezouska K., 2002, Rev. Mol. Biotechnol, V90, P269, DOI DOI 10.1016/S1389-0352(01)00064-2
[5]   Dendrimers in drug research [J].
Boas, U ;
Heegaard, PMH .
CHEMICAL SOCIETY REVIEWS, 2004, 33 (01) :43-63
[6]   Dendrimers, a new class of candidate topical microbicides with activity against herpes simplex virus infection [J].
Bourne, N ;
Stanberry, LR ;
Kern, ER ;
Holan, G ;
Matthews, B ;
Bernstein, DI .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (09) :2471-2474
[7]   Biological applications of dendrimers [J].
Cloninger, MJ .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2002, 6 (06) :742-748
[8]   SEQUENCE AND EXPRESSION OF A MEMBRANE-ASSOCIATED C-TYPE LECTIN THAT EXHIBITS CD4-INDEPENDENT BINDING OF HUMAN-IMMUNODEFICIENCY-VIRUS ENVELOPE GLYCOPROTEIN-GP120 [J].
CURTIS, BM ;
SCHARNOWSKE, S ;
WATSON, AJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (17) :8356-8360
[9]   DC-SIGN, a dendritic cell-specific HIV-1-binding protein that enhances trans-infection of T cells [J].
Geijtenbeek, TBH ;
Kwon, DS ;
Torensma, R ;
van Vliet, SJ ;
van Duijnhoven, GCF ;
Middel, J ;
Cornelissen, ILMHA ;
Nottet, HSLM ;
KewalRamani, VN ;
Littman, DR ;
Figdor, CG ;
van Kooyk, Y .
CELL, 2000, 100 (05) :587-597
[10]   Evidence of dual sites of action of dendrimers: SPL-2999 inhibits both virus entry and late stages of herpes simplex virus replication [J].
Gong, YH ;
Matthews, B ;
Cheung, D ;
Tam, T ;
Gadawski, I ;
Leung, D ;
Holan, G ;
Raff, J ;
Sacks, S .
ANTIVIRAL RESEARCH, 2002, 55 (02) :319-329