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 50 条
  • [21] Safety testing for replication-competent retrovirus associated with gibbon ape leukemia virus-pseudotyped retroviral vectors
    Chen, J
    Reeves, L
    Cornetta, K
    HUMAN GENE THERAPY, 2001, 12 (01) : 61 - 70
  • [22] Characterization of a replication-competent vector encoding DsRed based on a human adenovirus type 4 a-like strain
    Tian, Xingui
    Chen, Yong
    Li, Haitao
    Ran, Ye
    Zhou, Zhichao
    Chen, Shiying
    Li, Xiao
    Zhou, Rong
    VIRUS RESEARCH, 2019, 270
  • [23] Recruitment of wild-type and recombinant adeno-associated virus into adenovirus replication centers
    Weitzman, MD
    Fisher, KJ
    Wilson, JM
    JOURNAL OF VIROLOGY, 1996, 70 (03) : 1845 - 1854
  • [24] Efficient mobilization of E1-deleted adenovirus type 5 vectors by wild-type adenoviruses of other serotypes
    Rademaker, HJ
    Abou El Hassan, MA
    Versteeg, GA
    Rabelink, MJWE
    Hoeben, RC
    JOURNAL OF GENERAL VIROLOGY, 2002, 83 : 1311 - 1314
  • [25] Development of replication-competent retrovirus vectors for cancer gene therapy:: In vivo therapeutic efficacy, tumor-selectivity, and safety
    Tai, CK
    Wang, WJ
    Chen, TC
    Sazawa, A
    Faure, E
    Logg, CR
    Bochner, BH
    Yoon, LTK
    Lee, AS
    Cannon, PM
    Anderson, WF
    Kasahara, N
    CANCER GENE THERAPY, 2003, 10 : S15 - S15
  • [26] Adenovirus replication-competent vectors (KD1, KD3) complement the cytotoxicity and transgene expression from replication-defective vectors (Ad-GFP, Ad-Luc)
    Habib, NA
    Mitry, R
    Seth, P
    Kuppuswamy, M
    Doronin, K
    Toth, K
    Krajcsi, P
    Tollefson, AE
    Wold, WSM
    CANCER GENE THERAPY, 2002, 9 (08) : 651 - 654
  • [27] A cell line for high-yield production of E1-deleted adenovirus vectors without the emergence of replication-competent virus
    Gao, GP
    Engdahl, RK
    Wilson, JM
    HUMAN GENE THERAPY, 2000, 11 (01) : 213 - 219
  • [28] Wild-type p53 induction mediated by replication-deficient adenoviral vectors
    McPake, CR
    Shetty, S
    Kitchingman, GR
    Harris, LC
    CANCER RESEARCH, 1999, 59 (17) : 4247 - 4251
  • [29] A replication-competent adenovirus assay for E1-deleted Ad35 vectors produced in PER.C6 cells
    Marzio, G.
    Kerkvliet, E.
    Bogaards, J. A.
    Koelewijn, S.
    De Groot, A.
    Gijsbers, L.
    Weverling, G. J.
    Vogels, R.
    Havenga, M.
    Custers, J.
    Pau, M. G.
    Guichoux, J. Y.
    Lewis, J.
    Goudsmit, J.
    VACCINE, 2007, 25 (12) : 2228 - 2237
  • [30] Combined HSV-1 recombinant and amplicon piggyback vectors: Replication-competent and defective forms, and therapeutic efficacy for experimental gliomas
    Pechan, PA
    Herrlinger, U
    Aghi, M
    Jacobs, A
    Breakefield, XO
    JOURNAL OF GENE MEDICINE, 1999, 1 (03): : 176 - 185