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
  • [31] Toxicology and biodistribution of AdAPT-001, a replication-competent type 5 adenovirus with a trap for the immunosuppressive cytokine, TGF-beta
    Larson, Christopher
    Oronsky, Bryan
    Abrouk, Nacer E.
    Oronsky, Arnold
    Reid, Tony R.
    AMERICAN JOURNAL OF CANCER RESEARCH, 2021, 11 (10): : 5184 - 5189
  • [32] Evaluation of the biodistribution, persistence, toxicity, and potential of germ-line transmission of a replication-competent human adenovirus following intraprostatic administration in the mouse
    Paielli, DL
    Wing, MS
    Rogulski, KR
    Gilbert, JD
    Kolozsvary, A
    Kim, JH
    Hughes, J
    Schnell, M
    Thompson, T
    Freytag, SO
    MOLECULAR THERAPY, 2000, 1 (03) : 263 - 274
  • [33] Inclusion of miR122 targets in wild-type serotype 5 adenovirus to ablate liver replication
    Lavilla-Alonso, S.
    Ylosmaki, E.
    Saksela, K.
    HUMAN GENE THERAPY, 2010, 21 (10) : 1409 - 1409
  • [34] Attenuated, replication-competent herpes simplex virus type 1 mutant G207: Safety evaluation in mice
    Sundaresan, P
    Hunter, WD
    Martuza, RL
    Rabkin, SD
    JOURNAL OF VIROLOGY, 2000, 74 (08) : 3832 - 3841
  • [35] Complete replication-competent adenovirus 11p vectors with E1 or E3 insertions show improved heat stability
    Mei, Ya-Fang
    Wu, Haidong
    Hultenby, Kjell
    Silver, Jim
    VIROLOGY, 2016, 497 : 198 - 210
  • [36] Effects of viral strain, transgene position, and target cell type on replication kinetics, genomic stability, and transgene expression of replication-competent murine leukemia virus-based vectors
    Paar, Matthias
    Schwab, Sonja
    Rosenfellner, Doris
    Salmons, Brian
    Guenzburg, Walter H.
    Renner, Matthias
    Portsmouth, Daniel
    JOURNAL OF VIROLOGY, 2007, 81 (13) : 6973 - 6983
  • [37] Experimental therapy of allogeneic solid tumors induced in athymic mice with suicide gene-transducing replication-competent foamy virus vectors
    Martin Heinkelein
    Ursula Hoffmann
    Markus Lücke
    Horst Imrich
    Justus G Müller
    Jürgen Meixensberger
    Martin Westphahl
    Axel Kretschmer
    Axel Rethwilm
    Cancer Gene Therapy, 2005, 12 : 947 - 953
  • [38] Enhanced Safety Profiles of the Telomerase-Specific Replication-Competent Adenovirus by Incorporation of Normal Cell-Specific microRNA-Targeted Sequences
    Sugio, Kumiko
    Sakurai, Fuminori
    Katayama, Kazufumi
    Tashiro, Katsuhisa
    Matsui, Hayato
    Kawabata, Kenji
    Kawase, Atsushi
    Iwaki, Masahiro
    Hayakawa, Takao
    Fujiwara, Toshiyoshi
    Mizuguchi, Hiroyuki
    CLINICAL CANCER RESEARCH, 2011, 17 (09) : 2807 - 2818
  • [39] An adenoviral vector-based expression and delivery system for the inhibition of wild-type adenovirus replication by artificial microRNAs
    Ibrisimovic, Mirza
    Kneidinger, Doris
    Lion, Thomas
    Klein, Reinhard
    ANTIVIRAL RESEARCH, 2013, 97 (01) : 10 - 23
  • [40] Infectivity and expression of the early adenovirus proteins are important regulators of wild-type and ΔE1B adenovirus replication in human cells
    Wilma T Steegenga
    Nicole Riteco
    Johannes L Bos
    Oncogene, 1999, 18 : 5032 - 5043