A cleaved adhesin DNA vaccine targeting dendritic cell against Porphyromonas gingivalis-induced periodontal disease

被引:1
作者
Fan, Xin [1 ,2 ,3 ,4 ,5 ]
Qu, Peng-Yu [1 ]
Luan, Ke-Feng [1 ]
Sun, Chen-Yu [1 ]
Ren, Hui-Ping [2 ,3 ,4 ,5 ]
Sun, Xue-Hui [1 ]
Lan, Jing [2 ,3 ,4 ,5 ]
机构
[1] Shandong Second Med Univ, Affiliated Hosp, Dept Stomatol, 2428 Yuhe Rd, Weifang 261031, Shandong, Peoples R China
[2] Shandong Univ, Sch & Hosp Stomatol, 44-1 Wenhua Rd West, Jinan 250012, Shandong, Peoples R China
[3] Shandong Key Lab Oral Tissue Regenerat, 44-1 Wenhua Rd West, Jinan 250012, Shandong, Peoples R China
[4] Shandong Engn Lab Dent Mat & Oral Tissue Regenera, 44-1 Wenhua Rd West, Jinan 250012, Shandong, Peoples R China
[5] Shandong Prov Clin Res Ctr Oral Dis, 44-1 Wenhua Rd West, Jinan 250012, Shandong, Peoples R China
关键词
cleaved adhesin; dendritic cells; DNA vaccine; hemagglutinin adhesin; periodontal disease; Porphyromonas gingivalis; PROTECTIVE IMMUNITY; ARG-GINGIPAIN; BONE LOSS; RESPONSES; RGPA; IMMUNIZATION; HEMOGLOBIN; PROTEINASE; INFECTION; CCL19;
D O I
10.1111/omi.12465
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background: Arg-gingipain A (RgpA) is the primary virulence factor of Porphyromonas gingivalis and contains hemagglutinin adhesin (HA), which helps bacteria adhere to cells and proteins. Hemagglutinin's functional domains include cleaved adhesin (CA), which acts as a hemagglutination and hemoglobin-binding actor. Here, we confirmed that the HA and CA genes are immunogenic, and using adjuvant chemokine to target dendritic cells (DCs) enhanced protective autoimmunity against P. gingivalis-induced periodontal disease. Methods: C57 mice were immunized prophylactically with pVAX1-CA, pVAX1-HA, pVAX1, and phosphate-buffered saline (PBS) through intramuscular injection every 2 weeks for a total of three administrations before P. gingivalis-induced periodontitis. The DCs were analyzed using flow cytometry and ribonucleic acid sequencing (RNA-seq) transcriptomic assays following transfection with CA lentivirus. The efficacy of the co-delivered molecular adjuvant CA DNA vaccine was evaluated in vivo using flow cytometry, immunofluorescence techniques, and micro-computed tomography. Results: After the immunization, both the pVAX1-CA and pVAX1-HA groups exhibited significantly elevated P. gingivalis-specific IgG and IgG1, as well as a reduction in bone loss around periodontitis-affected teeth, compared to the pVAX1 and PBS groups (p < 0.05). The expression of CA promoted the secretion of HLA, CD86, CD83, and DC-specific intercellular adhesion molecule-3-grabbing non-integrin (DC-SIGN) in DCs. Furthermore, the RNA-seq analysis revealed a significant increase in the chemokine (C-C motif) ligand 19 (p < 0.05). A notable elevation in the quantities of DCs co-labeled with CD11c and major histocompatibility complex class II, along with an increase in interferon-gamma (IFN-gamma) cells, was observed in the inguinal lymph nodes of mice subjected to CCL19-CA immunization. This outcome effectively illustrated the preservation of peri-implant bone mass in rats afflicted with P. gingivalis-induced peri-implantitis (p < 0.05). Conclusions: The co-administration of a CCL19-conjugated CA DNA vaccine holds promise as an innovative and targeted immunization strategy against P. gingivalis-induced periodontitis and peri-implantitis.
引用
收藏
页码:433 / 445
页数:13
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