Stewart V Ann, McGrath Shannon, Krieg Arthur M, Larson Noelle S, Angov Evelina, Smith Christopher L, Brewer Thomas G, Heppner D Gray
Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Clin Vaccine Immunol. 2008 Feb;15(2):221-6. doi: 10.1128/CVI.00420-07. Epub 2007 Dec 12.
Following a demonstration that mouse-optimized cytosine-guanosine dinucleotide (CpG) oligodeoxynucleotides stimulated innate immune protection against intracellular pathogens, we tested the ability of CpG 7909, a primate-optimized Toll-like receptor 9 (TLR9) agonist, to stimulate rhesus macaques to produce interferon-inducible protein-10 (IP-10), a biomarker of immune activation. This study was performed prior to a similar trial with humans in order to facilitate the development of CpG 7909 as an immunomodulator for biodefense. A single subcutaneous dose of clinical-grade CpG 7909 was given to four groups of healthy adult rhesus macaques (0-mg dose [n = 5], 0.75-mg dose [n = 9], 1.5-mg dose [n = 9], and 3.0-mg dose [n = 9]). Directed physical examination findings, clinical laboratory values, and serum IP-10 concentrations were collected at scheduled intervals for 28 days. All three dose levels of CpG 7909 were safe and not associated with significant clinical or laboratory abnormality. The time to peak serum IP-10 concentration was 1.0 days at the 0.75-mg dose and 0.5 days at the 1.5- and 3.0-mg doses. A dose-dependent response was observed for the magnitude and duration of IP-10 concentrations, which remained significantly above baseline for 3 days for the 3.0-mg and 1.5-mg dose groups but above baseline for only 2 days for the 0.75-mg dose group. There were no nonresponders to CpG 7909. These rhesus macaque safety and IP-10 response data closely parallel a subsequent phase 1 human study of subcutaneously administered CpG 7909. A single dose of clinical-grade CpG 7909 induced a rapid, sustained IP-10 response, a biomarker for activation of the innate immune system. Given the similar susceptibilities of humans and rhesus macaques to infectious diseases, the rhesus macaque appears to be a suitable model to evaluate the potential of CpG 7909-mediated innate immune activation to protect humans against pathogens.
在证明小鼠优化的胞嘧啶-鸟嘌呤二核苷酸(CpG)寡脱氧核苷酸可刺激针对细胞内病原体的先天免疫保护后,我们测试了灵长类动物优化的Toll样受体9(TLR9)激动剂CpG 7909刺激恒河猴产生干扰素诱导蛋白10(IP-10)的能力,IP-10是免疫激活的生物标志物。这项研究在对人类进行类似试验之前进行,以促进将CpG 7909开发为用于生物防御的免疫调节剂。给四组健康成年恒河猴皮下注射单剂量临床级CpG 7909(0毫克剂量[n = 5]、0.75毫克剂量[n = 9]、1.5毫克剂量[n = 9]和3.0毫克剂量[n = 9])。在28天内按预定间隔收集定向体格检查结果、临床实验室值和血清IP-10浓度。CpG 7909的所有三个剂量水平都是安全的,且与显著的临床或实验室异常无关。血清IP-10浓度达到峰值的时间在0.75毫克剂量组为1.0天,在1.5毫克和3.0毫克剂量组为0.5天。观察到IP-10浓度的幅度和持续时间呈剂量依赖性反应,3.0毫克和1.5毫克剂量组在3天内显著高于基线水平,而0.75毫克剂量组仅在2天内高于基线水平。对CpG 7909没有无反应者。这些恒河猴的安全性和IP-10反应数据与随后皮下注射CpG 7909的1期人体研究密切相似。单剂量临床级CpG 7909诱导了快速、持续的IP-10反应,IP-10是先天免疫系统激活的生物标志物。鉴于人类和恒河猴对传染病的易感性相似,恒河猴似乎是评估CpG 7909介导的先天免疫激活保护人类抵御病原体潜力的合适模型。