Primary Leukocyte Screens for Innate Immune Agonists

被引:10
作者
Goodchild, Amber [1 ]
Nopper, Nicole [1 ]
Craddock, Alexis [1 ]
Law, Tamara [1 ]
King, Andrew [1 ]
Fanning, Gregory [2 ]
Rivory, Laurent [1 ]
Passioura, Toby [1 ]
机构
[1] Johnson & Johnson Res Pty Ltd, Strawberry Hills, NSW 2012, Australia
[2] Tibotec Pharmaceut, Little Isl, County Cork, Ireland
关键词
innate immune agonists; high-throughput screening; Toll-like receptors; immunostimulants; TOLL-LIKE RECEPTOR-3; DOUBLE-STRANDED-RNA; EPITHELIAL-CELLS; HEPATITIS-C; LOCALIZATION; ACTIVATION; RESPONSES;
D O I
10.1177/1087057109335325
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The innate immune system of mammals is a key defense mechanism against invading foreign pathogens. Innate immune stimulants may have applications as vaccine adjuvants as well as in the treatment of cancer and some viral diseases, and clinical studies have been performed using agonists of Toll-like receptors (TLRs) 7, 8, and 9. The high-throughput screens for such agonists have typically relied on the overexpression of a single TLR gene in an immortalized cell line and are inherently artificial systems that are restricted to the identification of agonists for a single receptor. The authors describe 2 assays for the identification of immunostimulants that employ primary human leukocytes cocultured with hepatitis C virus (HCV) replicon-expressing cells. In these assays, stimulation of innate immune pathways in leukocytes induces interferon (IFN) expression, which acts to inhibit HCV replication, providing a high-throughput and low-cost readout for leukocyte activation. These assays are highly sensitive and provide a physiologically relevant system for the identification of a broad range of immunostimulant agents. (Journal of Biomolecular Screening 2009:723-730)
引用
收藏
页码:723 / 730
页数:8
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