Role of αv integrins in adenovirus cell entry and gene delivery

被引:221
作者
Nemerow, GR [1 ]
Stewart, PL [1 ]
机构
[1] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
关键词
D O I
10.1128/MMBR.63.3.725-734.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Adenoviruses (Ad) are a significant cause of acute infections in humans; however, replication-defective forms of this virus are currently under investigation for human gene therapy Approximately 20 to 25% of all the gene therapy trials (phases I to III) conducted over the past 10 years involve the use of Ad gene delivery for treatment inherited or acquired diseases. At present, the most promising applications involve the use of Ad vectors to irradicate certain nonmetastatic tumors and to promote angiogenesis in order to alleviate cardiovascular disease. While specific problems of using Ad vectors remain to be overcome las is true for almost all viral and nonviral delivery methods), a distinct advantage of Ad is the extensive knowledge of its macromolecular structure, genome organization, sequence, and mode of replication. Moreover, significant information has also been acquired on the interaction of Ad particles with distinct host cell receptors, events which strongly affect virus tropism. This review provides an overview of the structure and function of Ad attachment (coxsackievirus and Ad receptor [CAR]) and internalization (alpha(nu) integrins) receptors and discusses their precise role in virus infection and gene delivery. Recent structure studies of integrin-Ad complexes by cryoelectron microscopy are also highlighted. Finally, unanswered questions arising from the current state of knowledge of Ad-receptor interactions are presented in the context of improving Ad vectors for future human gene therapy applications.
引用
收藏
页码:725 / +
页数:12
相关论文
共 106 条
[101]   Targeted adenovirus-mediated gene delivery to T cells via CD3 [J].
Wickham, TJ ;
Lee, GM ;
Titus, JA ;
Sconocchia, G ;
Bakacs, T ;
Kovesdi, I ;
Segal, DM .
JOURNAL OF VIROLOGY, 1997, 71 (10) :7663-7669
[102]   INTEGRIN ALPHA-V-BETA-5 SELECTIVELY PROMOTES ADENOVIRUS-MEDIATED CELL-MEMBRANE PERMEABILIZATION [J].
WICKHAM, TJ ;
FILARDO, EJ ;
CHERESH, DA ;
NEMEROW, GR .
JOURNAL OF CELL BIOLOGY, 1994, 127 (01) :257-264
[103]   INTEGRIN-ALPHA-V-BETA-3 AND INTEGRIN-ALPHA-V-BETA-5 PROMOTE ADENOVIRUS INTERNALIZATION BUT NOT VIRUS ATTACHMENT [J].
WICKHAM, TJ ;
MATHIAS, P ;
CHERESH, DA ;
NEMEROW, GR .
CELL, 1993, 73 (02) :309-319
[104]   A p300/CBP-associated factor that competes with the adenoviral oncoprotein E1A [J].
Yang, XJ ;
Ogryzko, VV ;
Nishikawa, J ;
Howard, BH ;
Nakatani, Y .
NATURE, 1996, 382 (6589) :319-324
[105]   ADENOVIRUS-MEDIATED GENE-TRANSFER TRANSIENTLY CORRECTS THE CHLORIDE TRANSPORT DEFECT IN NASAL EPITHELIA OF PATIENTS WITH CYSTIC-FIBROSIS [J].
ZABNER, J ;
COUTURE, LA ;
GREGORY, RJ ;
GRAHAM, SM ;
SMITH, AE ;
WELSH, MJ .
CELL, 1993, 75 (02) :207-216
[106]   Lack of high affinity fiber receptor activity explains the resistance of ciliated airway epithelia to adenovirus infection [J].
Zabner, J ;
Freimuth, P ;
Puga, A ;
Fabrega, A ;
Welsh, MJ .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (05) :1144-1149