Karaolis David K R, Newstead Michael W, Zeng Xianying, Hyodo Mamoru, Hayakawa Yoshihiro, Bhan Urvhashi, Liang Hallie, Standiford Theodore J
Intragenics Research Institute, Havre de Grace, MD 21078, USA.
Infect Immun. 2007 Oct;75(10):4942-50. doi: 10.1128/IAI.01762-06. Epub 2007 Jul 23.
Innate immunity is the primary mechanism by which extracellular bacterial pathogens are effectively cleared from the lung. We have previously shown that cyclic di-GMP (c-di-GMP [c-diguanylate]) is a novel small molecule immunomodulator and immunostimulatory agent that triggers protective host innate immune responses. Using a murine model of bacterial pneumonia, we show that local intranasal (i.n.) or systemic subcutaneous (s.c.) administration of c-di-GMP prior to intratracheal (i.t.) challenge with Klebsiella pneumoniae stimulates protective immunity against infection. Specifically, i.n. or s.c. administration of c-di-GMP 48 and 24 h prior to i.t. K. pneumoniae challenge resulted in significantly increased survival. Pretreatment with c-di-GMP resulted in a 5-fold reduction in bacterial CFU in the lung (P < 0.05) and an impressive >1,000-fold decrease in CFU in the blood (P < 0.01). c-di-GMP administration stimulated a robust innate response to bacterial challenge, characterized by enhanced accumulation of neutrophils and alphabeta T cells, as well as activated NK and alphabeta T lymphocytes, which was associated with earlier and more vigorous expression of chemokines and type I cytokines. Moreover, lung macrophages recovered from Klebsiella-infected mice pretreated with c-di-GMP expressed greater quantities of inducible nitric oxide synthase and nitric oxide ex vivo than did macrophages isolated from infected mice pretreated with the control, c-GMP. These findings demonstrate that c-di-GMP delivered in either a compartmentalized or systemic fashion stimulates protective innate immunity in the lung and protects mice against bacterial invasion. We propose that the cyclic dinucleotide c-di-GMP may be used clinically as an effective immunomodulator, immune enhancer, and vaccine adjuvant to protect against respiratory infection and pneumonia in humans and animals.
天然免疫是从肺部有效清除细胞外细菌病原体的主要机制。我们之前已经表明,环二鸟苷酸(c-di-GMP [环二鸟苷酸])是一种新型小分子免疫调节剂和免疫刺激剂,可触发保护性宿主天然免疫反应。使用细菌性肺炎小鼠模型,我们发现,在气管内(i.t.)用肺炎克雷伯菌攻击之前,局部鼻内(i.n.)或全身皮下(s.c.)给予c-di-GMP可刺激针对感染的保护性免疫。具体而言,在i.t.肺炎克雷伯菌攻击前48小时和24小时进行i.n.或s.c.给予c-di-GMP可显著提高存活率。用c-di-GMP预处理可使肺部细菌CFU减少5倍(P < 0.05),血液中CFU减少超过1000倍(P < 0.01)。给予c-di-GMP可刺激对细菌攻击的强烈天然免疫反应,其特征是中性粒细胞和αβ T细胞的积累增加,以及NK和αβ T淋巴细胞的活化,这与趋化因子和I型细胞因子的更早、更强烈表达有关。此外,与从用对照c-GMP预处理的感染小鼠中分离的巨噬细胞相比,从用c-di-GMP预处理的肺炎克雷伯菌感染小鼠中回收的肺巨噬细胞在体外表达更多的诱导型一氧化氮合酶和一氧化氮。这些发现表明,以分隔或全身方式递送的c-di-GMP可刺激肺部的保护性天然免疫,并保护小鼠免受细菌入侵。我们建议,环二核苷酸c-di-GMP可在临床上用作有效的免疫调节剂、免疫增强剂和疫苗佐剂,以预防人和动物的呼吸道感染和肺炎。