Ogunniyi Abiodun D, Paton James C, Kirby Alun C, McCullers Jonathan A, Cook Jan, Hyodo Mamoru, Hayakawa Yoshihiro, Karaolis David K R
School of Molecular and Biomedical Science, University of Adelaide, South Australia 5005, Australia.
Vaccine. 2008 Aug 26;26(36):4676-85. doi: 10.1016/j.vaccine.2008.06.099. Epub 2008 Jul 18.
Cyclic diguanylate (c-di-GMP) is a unique bacterial intracellular signaling molecule capable of stimulating enhanced protective innate immunity against various bacterial infections. The effects of intranasal pretreatment with c-di-GMP, or intraperitoneal coadministration of c-di-GMP with the pneumolysin toxoid (PdB) or pneumococcal surface protein A (PspA) before pneumococcal challenge, were investigated in mice. We found that c-di-GMP had no significant direct short-term effect on the growth rate of Streptococcus pneumoniae either in vitro or in vivo. However, intranasal pretreatment of mice with c-di-GMP resulted in a significant decrease in bacterial load in lungs and blood after serotypes 2 and 3 challenge, and a significant decrease in lung titers after serotype 4 challenge. Potential cellular mediators of these enhanced protective responses were identified in lungs and draining lymph nodes. Intraperitoneal coadministration of c-di-GMP with PdB or PspA before challenge resulted in significantly higher antigen-specific antibody titers and increased survival of mice, compared to that obtained with alum adjuvant. These findings demonstrate that local or systemic c-di-GMP administration stimulates innate and adaptive immunity against invasive pneumococcal disease. We propose that c-di-GMP can be used as an effective broad spectrum immunomodulator and vaccine adjuvant to prevent infectious diseases.
环二鸟苷酸(c-di-GMP)是一种独特的细菌细胞内信号分子,能够刺激增强针对各种细菌感染的先天性免疫保护作用。我们在小鼠中研究了鼻内用c-di-GMP预处理,或在肺炎球菌攻击前腹腔内将c-di-GMP与肺炎溶血素类毒素(PdB)或肺炎球菌表面蛋白A(PspA)联合给药的效果。我们发现,c-di-GMP在体外或体内对肺炎链球菌的生长速率均无显著直接短期影响。然而,用c-di-GMP对小鼠进行鼻内预处理后,在2型和3型血清型攻击后,肺和血液中的细菌载量显著降低,在4型血清型攻击后,肺滴度显著降低。在肺和引流淋巴结中鉴定出了这些增强的保护反应的潜在细胞介质。与明矾佐剂相比,在攻击前腹腔内将c-di-GMP与PdB或PspA联合给药导致抗原特异性抗体滴度显著更高,小鼠存活率增加。这些发现表明,局部或全身给予c-di-GMP可刺激针对侵袭性肺炎球菌疾病的先天性和适应性免疫。我们提出,c-di-GMP可作为一种有效的广谱免疫调节剂和疫苗佐剂来预防传染病。