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Oral Mucosal Immunization Recent Advancement and Exploit Dendritic Cell Targeting

机译:口腔粘膜免疫的最新进展和利用树突状细胞靶向

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Oral mucosal vaccine thrive significant interest in developing vaccines that evoke mucosal moreover systemic immune response i.e. induction of IgA. Oral immunization consistently preferred over conventional immunization because it provides strengthens inpatient acquiescence, needle-free delivery, cost-effective. Thereby strong antibody production at the mucosal site is not refreshing by parenteral administration of the vaccines. Antibodies produced on the mucosal surface instead of it also start common mucosal immune system (CMIS). Vaccines allow particulate delivery protection of antigen. Polylactic-co-glycolic acid, poly lactic acid loaded nanoparticles, liposomes, niosomes, dendrimers; proteosomes are some of the nanocarriers which protect the antigen from their degradation. Authentication concepts of various studies on the mucosal vaccine by using nanotechnology for targeting to dendritic cell presenting on Peyer's patch elicit antibody production. This review sums up current studies on mucosal vaccination by using nanocarrier. More of the studies have been done on mucosal for improvement in methodology.
机译:口服粘膜疫苗在开发引起粘膜而且全身免疫应答即IgA诱导的疫苗方面引起了极大的兴趣。口服免疫始终优于常规免疫,因为它可增强住院患者的默认水平,无针递送,经济高效。因此,通过肠胃外施用疫苗,在粘膜部位的强抗体产生不会恢复。在粘膜表面而不是表面产生的抗体也会启动普通的粘膜免疫系统(CMIS)。疫苗可保护抗原的微粒传递。聚乳酸-乙醇酸共聚物,载有聚乳酸的纳米颗粒,脂质体,脂质体,树枝状聚合物;蛋白体是保护抗原免于其降解的一些纳米载体。对粘膜疫苗的各种研究的验证概念,是通过使用针对Peyer贴片的呈递树突状细胞的纳米技术来引发抗体产生的。这篇综述总结了目前使用纳米载体进行粘膜疫苗接种的研究。为了改善方法,已经进行了关于粘膜的更多研究。

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