Yan Yan-Hong, Yu Fei, Zeng Chang, Cao Li-Hua, Zhang Zhou, Xu Qing-An
The State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST) & Key Laboratory of Oral Biomedicine of Ministry of Education (KLOBM), School & Hospital of Stomatology, Wuhan University, Wuhan 430079, China.
Shanghai Engineering Research Center of Tooth Restoration and Regeneration, Department of Pediatric Dentistry, School of Stomatology, Tongji University, Shanghai 200072, China.
Acta Pharmacol Sin. 2016 Sep;37(9):1229-36. doi: 10.1038/aps.2016.73. Epub 2016 Aug 15.
CCL19 and its receptor CCR7 are essential molecules for facilitating the trafficking of mature dendritic cells (DCs) and helping to establish a microenvironment in lymphoid tissues to initiate primary immune responses, whereas CCL17 is required in the CCR7-CCL19-dependent migration of DCs. In this study we examined whether co-administration of CCL17 and CCL19 could enhance the immunogenicity of an anti-caries DNA vaccine, pCIA-P, in rodents.
Plasmids encoding CCL17 (pCCL17/VAX) and CCL19 (pCCL19/VAX) were constructed. BALB/c mice were intranasally administered pCCL17/VAX, pCCL19/VAX, or pCCL17/VAX plus pCCL19/VAX, the migration of DCs to the spleen and draining lymph nodes (DLNs) was assessed with flow cytometry. The mice were co-administered pCIA-P; and the anti-PAc antibodies in the serum and saliva were detected with ELISA. Wistar rats were orally challenged with Streptococcus mutans and then administered pCIA-P in combination with pCCL17/VAX, pCCL19/VAX, or pCCL17/VAX plus pCCL19/VAX. The amount of S mutans sustained on rat molar surfaces was assessed using a colony forming assay. Caries activity was scored with the Keyes method.
Co-administration of the CCL17 and CCL19 genes in mice caused a greater increase in the number of mature DCs in the spleen and DLNs compared with administration of CCL17 or CCL19 genes alone. CCL17 and CCL19 double-adjuvant plus pCIA-P induced significantly higher levels of anti-PAc salivary IgA and anti-PAc serum IgG antibody in mice, and strengthened the ability of pCIA-P in inhibiting the colonization of S mutans on rat tooth surfaces. The caries activity of the combined adjuvant group was significantly lower than that of the pCCL17/VAX or the pCCL19/VAX group.
A nasal adjuvant consisting of a combination of CCL17 and CCL19 attracts more mature DCs to secondary lymphoid tissues, inducing enhanced antibody responses against the anti-caries DNA vaccine pCIA-P and reducing S mutans infection in rodents.
CCL19及其受体CCR7是促进成熟树突状细胞(DCs)迁移并帮助在淋巴组织中建立微环境以启动初次免疫反应的关键分子,而CCL17是DCs依赖CCR7-CCL19迁移所必需的。在本研究中,我们检测了联合给予CCL17和CCL19是否能增强抗龋DNA疫苗pCIA-P在啮齿动物中的免疫原性。
构建编码CCL17(pCCL17/VAX)和CCL19(pCCL19/VAX)的质粒。将pCCL17/VAX、pCCL19/VAX或pCCL17/VAX加pCCL19/VAX经鼻给予BALB/c小鼠,用流式细胞术评估DCs向脾脏和引流淋巴结(DLNs)的迁移。给小鼠联合给予pCIA-P;用ELISA检测血清和唾液中的抗PAc抗体。用变形链球菌对Wistar大鼠进行口腔攻击,然后给予pCIA-P联合pCCL17/VAX、pCCL19/VAX或pCCL17/VAX加pCCL19/VAX。用菌落形成试验评估大鼠磨牙表面变形链球菌的存留量。用凯斯方法对龋齿活性进行评分。
与单独给予CCL17或CCL19基因相比,在小鼠中联合给予CCL17和CCL19基因导致脾脏和DLNs中成熟DCs数量有更大增加。CCL17和CCL19双佐剂加pCIA-P在小鼠中诱导出显著更高水平的抗PAc唾液IgA和抗PAc血清IgG抗体,并增强了pCIA-P抑制变形链球菌在大鼠牙齿表面定植的能力。联合佐剂组的龋齿活性显著低于pCCL17/VAX或pCCL19/VAX组。
由CCL17和CCL19组成的鼻腔佐剂可吸引更多成熟DCs至二级淋巴组织,诱导针对抗龋DNA疫苗pCIA-P的增强抗体反应,并减少啮齿动物中的变形链球菌感染。