The Influence of Innate and Pre-Existing Immunity on Adenovirus Therapy

被引:115
作者
Zaiss, Anne K. [1 ,2 ,3 ]
Machado, Hidevaldo B. [1 ,2 ,3 ]
Herschman, Harvey R. [1 ,2 ,3 ,4 ]
机构
[1] Univ Calif Los Angeles, Dept Biol Chem, David Geffen Sch Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Mol & Med Pharmacol, David Geffen Sch Med, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Inst Mol Biol, David Geffen Sch Med, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Jonsson Comprehens Canc Ctr, David Geffen Sch Med, Los Angeles, CA 90095 USA
关键词
ADENOVIRUS; INNATE IMMUNITY; NEUTRALIZING ANTIBODY; GENE THERAPY; VACCINATION; HELPER-DEPENDENT ADENOVIRUS; SIGNIFICANT GENE-EXPRESSION; IN-VIVO; RECOMBINANT ADENOVIRUS; NEUTRALIZING ANTIBODIES; POLYETHYLENE-GLYCOL; HIGH-CAPACITY; T-CELLS; IMMUNOLOGICAL SYNAPSES; ADENOASSOCIATED VIRUS;
D O I
10.1002/jcb.22328
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recombinant adenovirus serotype 5 (Ad5) vectors have been studied extensively in preclinical gene therapy models and in a range of clinical trials. However, innate immune responses to adenovirus vectors limit effectiveness of Ad5 based therapies. Moreover, extensive pre-existing Ad5 immunity in human populations will likely limit the clinical utility of adenovirus vectors, unless methods to circumvent neutralizing antibodies that bind virus and block target cell transduction can be developed. Furthermore, memory T cell and humoral responses to Ad5 are associated with increased toxicity, raising safety concerns for therapeutic adenovirus vectors in immunized hosts. Most preclinical studies have been performed in naive animals; although pre-existing immunity is among the greatest hurdles for adenovirus therapies, it is also one of the most neglected experimentally. Here we summarize findings using adenovirus vectors in naive animals, in Ad-immunized animals and in clinical trials, and review strategies proposed to overcome innate immune responses and pre-existing immunity. J. Cell. Biochem. 108: 778-790, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:778 / 790
页数:13
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