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首页> 外文期刊>Brazilian Archives of Biology and Technology >A Therapeutic Oral Vaccine Candidate against Propionibacterium acnes: Preparation and Immunological Evaluation of Nanoparticles Encapsulated Sialidase-CAMP Fusion Protein
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A Therapeutic Oral Vaccine Candidate against Propionibacterium acnes: Preparation and Immunological Evaluation of Nanoparticles Encapsulated Sialidase-CAMP Fusion Protein

机译:针对丙酸杆菌的治疗口腔疫苗候选者:纳米颗粒的制备和免疫评估包封唾液酸酶蛋白融合蛋白

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Acne Vulgaris is a common skin disease caused by Propionibacterium acnes , an anaerobic microbiota of human skin that plays a vital role in the pathology of acne. The aim of this study was to prepare nanoparticles containing an acne recombinant protein and determine its ability as an oral acne vaccine in mice. The recombinant Sialidase-CAMP gene was expressed and purified in a prokaryotic host. The chitosan nanoparticles containing the recombinant protein were prepared, encapsulated, and administered by both oral and subcutaneous routes to Balb/c mice. Sera IgA and IgG and stool IgA titers were measured by ELISA, and the immunized mice were challenged against P. acnes . A 65 kDa recombinant protein was confirmed by SDS-PAGE and western blot. The size and zeta potential of nanoparticles were 80 nm and 18 mV, respectively. After oral immunization, the serum IgG and IgA titers were 1:3200 and 1:16, respectively, and the stool IgA titer was 1:8. In the subcutaneous route, the serum IgG titer was 1:51200. Immunized mice showed no inflammation in the ear of challenged mice. It is the first study that examines a chitosan-nanoparticulated acne fusion protein as an applicable acne vaccine candidate with appropriate immunogenicity potential. Further studies are required to validate the clinical usefulness of this vaccine candidate.
机译:痤疮寻常症是由痤疮丙酸杆菌丙酸杆菌痤疮丙酸杆菌引起的常见皮肤病,这是人体皮肤的厌氧微生物,在痤疮的病理学中起着至关重要的作用。本研究的目的是制备含有痤疮重组蛋白的纳米颗粒,并确定其作为小鼠口腔痤疮疫苗的能力。在原核宿主中表达并纯化重组唾液酸酶-CAP基因。制备含有重组蛋白的壳聚糖纳米粒子,用口服和皮下途径制备,包封并给予BALB / C小鼠。通过ELISA测量血清IgA和IgG和粪便IgA滴度,免疫小鼠攻击P. Acnes。通过SDS-PAGE和Western印迹确认65kDa重组蛋白。纳米颗粒的尺寸和ζ电位分别为80nm和18mV。在口腔免疫后,血清IgG和IgA滴度分别为1:3200和1:16,粪便IgA滴度为1:8。在皮下途径中,血清IgG滴度为1:51200。免疫小鼠在挑战小鼠的耳朵中显示出炎症。第一项研究将壳聚糖 - 纳米颗粒状痤疮融合蛋白作为适用的痤疮疫苗候选物,具有适当的免疫原性潜力。需要进一步的研究来验证该疫苗候选者的临床有用性。

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