Experimental infections of humans with wild-type adenoviruses and with replication-competent adenovirus vectors: replication, safety, and transmission

被引:56
作者
Lichtenstein, DL
Wold, WS
机构
[1] St Louis Univ, Sch Med, Dept Mol Microbiol & Immunol, St Louis, MO 63104 USA
[2] VirRx Inc, St Louis, MO 63017 USA
关键词
adenovirus; replication-competent vectors; human; clinical trials; review;
D O I
10.1038/sj.cgt.7700765
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Replication-competent (RC) adenoviruses (Ads) are increasingly being developed as oncolytic vectors and as vehicles for delivering vaccine antigens. Although the safety of such vectors in humans is of paramount importance, these vectors pose additional special concerns. Specifically, the prospect of causing Ad-mediated disease in the patient, the amount and sites of Ad replication, the possibility of virus shedding leading to unintended transmission to patient contacts, and the potential for persistence in the inoculated individual must be evaluated. Previous experience with administration of wild-type and RC recombinant Ads to humans may shed light on some of these issues. Experimental infections of humans with natural Ad isolates and RC recombinant vectors show that in adults Ads cause mild or no disease, particularly with Ad serotypes 2 and 5, the serotypes most often used to make recombinant constructs. Other studies show that Ad can replicate in experimentally infected persons, that in some situations Ads can be shed and transmitted to close contacts, and that there is evidence for persistent/latent Ad infection in naturally infected individuals. Overall, these studies indicate that Ads can be safely administered to humans for the treatment of cancer and as antigen delivery vehicles suggesting that the continued development of RC oncolytic and vaccine vectors should be pursued.
引用
收藏
页码:819 / 829
页数:11
相关论文
共 111 条
[61]  
Macek V, 1999, Can Respir J, V6, P37
[62]  
Makower D, 2003, CLIN CANCER RES, V9, P693
[63]   Persistence of viruses in upper respiratory tract of children with asthma [J].
Marin, J ;
Jeler-Kacar, D ;
Levstek, V ;
Macek, V .
JOURNAL OF INFECTION, 2000, 41 (01) :69-72
[64]  
Matsubara S, 2001, CANCER RES, V61, P6012
[65]   LATENT ADENOVIRAL INFECTION IN THE PATHOGENESIS OF CHRONIC AIRWAYS OBSTRUCTION [J].
MATSUSE, T ;
HAYASHI, S ;
KUWANO, K ;
KEUNECKE, H ;
JEFFERIES, WA ;
HOGG, JC .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1992, 146 (01) :177-184
[66]  
MITSUI Y, 1959, Br J Ophthalmol, V43, P540, DOI 10.1136/bjo.43.9.540
[67]   EFFECT OF INOCULATING ADENOVIRUS (APC VIRUS) TYPE-8 INTO HUMAN VOLUNTEERS [J].
MITSUI, Y ;
HANABUSA, J ;
MINODA, R ;
OGATA, S .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1957, 43 (04) :84-90
[68]   COMMUNICABILITY OF ENTERIC LIVE ADENOVIRUS TYPE 4 VACCINE IN FAMILIES [J].
MUELLER, RE ;
MULDOON, RL ;
JACKSON, GG .
JOURNAL OF INFECTIOUS DISEASES, 1969, 119 (01) :60-&
[69]   Safety and feasibility of injection with an E1B-55 kDa gene-deleted, replication-selective adenovirus (ONYX-015) into primary carcinomas of the pancreas: a phase I trial [J].
Mulvihlll, S ;
Warren, R ;
Venook, A ;
Adler, A ;
Randlev, B ;
Heise, C ;
Kirn, D .
GENE THERAPY, 2001, 8 (04) :308-315
[70]   Adenoviral gene therapy leads to rapid induction of multiple chemokines and acute neutrophil-dependent hepatic injury in vivo [J].
Muruve, DA ;
Barnes, MJ ;
Stillman, IE ;
Libermann, TA .
HUMAN GENE THERAPY, 1999, 10 (06) :965-976