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
[1]  
[Anonymous], 2002, Hum Gene Ther, V13, P3
[2]   The genetics and genomics of cancer [J].
Balmain, A ;
Gray, J ;
Ponder, B .
NATURE GENETICS, 2003, 33 (Suppl 3) :238-244
[3]   LATENT ADENOVIRAL INFECTION IN FOLLICULAR BRONCHIECTASIS [J].
BATEMAN, ED ;
HAYASHI, S ;
KUWANO, K ;
WILKE, TA ;
HOGG, JC .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1995, 151 (01) :170-176
[4]   STUDIES OF ADENOVIRUSES (APC) IN VOLUNTEERS [J].
BELL, JA ;
WARD, TG ;
HUEBNER, RJ ;
ROWE, WP ;
SUSKING, RG ;
PAFFENBARGER, RS .
AMERICAN JOURNAL OF PUBLIC HEALTH AND THE NATIONS HEALTH, 1956, 46 (09) :1130-1146
[5]  
Benjamin R, 2001, Hum Gene Ther, V12, P1591
[6]  
BHAT BM, 1994, VACCINES 94 - MODERN APPROACHES TO NEW VACCINES INCLUDING PREVENTION OF AIDS, P309
[7]   An adenovirus mutant that replicates selectively in p53-deficient human tumor cells [J].
Bischoff, JR ;
Kim, DH ;
Williams, A ;
Heise, C ;
Horn, S ;
Muna, M ;
Ng, L ;
Nye, JA ;
SampsonJohannes, A ;
Fattaey, A ;
McCormick, F .
SCIENCE, 1996, 274 (5286) :373-376
[8]   IMMUNIZATION BY SELECTIVE INFECTION WITH TYPE 4 ADENOVIRUS GROWN IN HUMAN DIPLOID TISSUE CULTURE .I. SAFETY AND LACK OF ONCOGENICITY AND TESTS FOR POTENCY IN VOLUNTEERS [J].
CHANOCK, RM ;
LUDWIG, W ;
HEUBNER, RJ ;
CATE, TR ;
CHU, LW .
JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1966, 195 (06) :445-&
[9]   Replication and immunogenicity of Ad7-, Ad4-, and Ad5-hepatitis B virus surface antigen recombinants, with or without a portion of E3 region, in chimpanzees [J].
Chengalvala, MV ;
Bhat, BM ;
Bhat, RA ;
Dheer, SK ;
Lubeck, MD ;
Purcell, RH ;
Murthy, KK .
VACCINE, 1997, 15 (03) :335-339
[10]  
*COMM AC RESP DIS, 1947, J CLIN INVEST, V26, P957