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介孔二氧化硅纳米颗粒作为抗结核疫苗开发的潜在平台

Mesoporous Silica Nanoparticles as a Potential Platform for Vaccine Development against Tuberculosis.

作者信息

Montalvo-Quirós Sandra, Vallet-Regí María, Palacios Ainhoa, Anguita Juan, Prados-Rosales Rafael C, González Blanca, Luque-Garcia Jose L

机构信息

Department of Analytical Chemistry, Faculty of Chemistry, Complutense University of Madrid, 28040 Madrid, Spain.

Centro de Estudios Tecnológicos y Sociales y Facultad de Experimentales, Francisco de Vitoria University, 28223 Madrid, Spain.

出版信息

Pharmaceutics. 2020 Dec 16;12(12):1218. doi: 10.3390/pharmaceutics12121218.

Abstract

The increasing emergence of new strains of () highly resistant to antibiotics constitute a public health issue, since tuberculosis still constitutes the primary cause of death in the world due to bacterial infection. has been shown to produce membrane-derived extracellular vesicles (EVs) containing proteins responsible for modulating the pathological immune response after infection. These natural vesicles were considered a promising alternative to the development of novel vaccines. However, their use was compromised by the observed lack of reproducibility between preparations. In this work, with the aim of developing nanosystems mimicking the extracellular vesicles produced by mesoporous silica nanoparticles (MSNs) have been used as nanocarriers of immunomodulatory and vesicle-associated proteins (Ag85B, LprG and LprA). These novel nanosystems have been designed and extensively characterized, demonstrating the effectiveness of the covalent anchorage of the immunomodulatory proteins to the surface of the MSNs. The immunostimulatory capacity of the designed nanosystems has been demonstrated by measuring the levels of pro- (TNF) and anti-inflammatory (IL-10) cytokines in exposed macrophages. These results open a new possibility for the development of more complex nanosystems, including additional vesicle components or even antitubercular drugs, thus allowing for the combination of immunomodulatory and bactericidal effects against .

摘要

对多种抗生素具有高度抗性的新型()菌株不断出现,这构成了一个公共卫生问题,因为结核病仍是全球细菌感染导致死亡的主要原因。()已被证明能产生膜衍生的细胞外囊泡(EVs),其中含有负责调节感染后病理免疫反应的蛋白质。这些天然囊泡被认为是开发新型疫苗的一个有前景的替代方案。然而,由于制剂之间缺乏可重复性,其应用受到了影响。在这项工作中,为了开发模仿()产生的细胞外囊泡的纳米系统,介孔二氧化硅纳米颗粒(MSNs)被用作免疫调节和囊泡相关蛋白(Ag85B、LprG和LprA)的纳米载体。这些新型纳米系统已经过设计和广泛表征,证明了免疫调节蛋白与MSNs表面共价锚定的有效性。通过测量暴露巨噬细胞中促炎(TNF)和抗炎(IL - 10)细胞因子的水平,证明了所设计纳米系统的免疫刺激能力。这些结果为开发更复杂的纳米系统开辟了新的可能性,包括添加其他囊泡成分甚至抗结核药物,从而实现针对()的免疫调节和杀菌效果的联合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bded/7767215/655ce04681bd/pharmaceutics-12-01218-g003.jpg

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