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用于巴西利什曼原虫抗原无针纳米疫苗接种的超可变形古脂质体

Ultradeformable Archaeosomes for Needle Free Nanovaccination with Leishmania braziliensis Antigens.

作者信息

Higa Leticia H, Arnal Laura, Vermeulen Mónica, Perez Ana Paula, Schilrreff Priscila, Mundiña-Weilenmann Cecilia, Yantorno Osvaldo, Vela María Elena, Morilla María José, Romero Eder Lilia

机构信息

Nanomedicine Research Program, Departamento de Ciencia y Tecnologia, Universidad Nacional de Quilmes. Roque Saenz Peña 352, Bernal, Argentina B1876BXD.

Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas (INIFTA), Universidad Nacional de La Plata-CONICET, Sucursal 4 Casilla de Correo 16, 1900 La Plata, Argentina.

出版信息

PLoS One. 2016 Mar 2;11(3):e0150185. doi: 10.1371/journal.pone.0150185. eCollection 2016.

Abstract

Total antigens from Leishmania braziliensis promastigotes, solubilized with sodium cholate (dsLp), were formulated within ultradeformable nanovesicles (dsLp-ultradeformable archaeosomes, (dsLp-UDA), and dsLp-ultradeformable liposomes (dsLp-UDL)) and topically administered to Balb/c mice. Ultradeformable nanovesicles can penetrate the intact stratum corneum up to the viable epidermis, with no aid of classical permeation enhancers that can damage the barrier function of the skin. Briefly, 100 nm unilamellar dsLp-UDA (soybean phosphatidylcholine: Halorubrum tebenquichense total polar lipids (TPL): sodium cholate, 3:3:1 w:w) of -31.45 mV Z potential, containing 4.84 ± 0.53% w/w protein/lipid dsLp, 235 KPa Young modulus were prepared. In vitro, dsLp-UDA was extensively taken up by J774A1 and bone marrow derive cells, and the only that induced an immediate secretion of IL-6, IL-12p40 and TNF-α, followed by IL-1β, by J774A1 cells. Such extensive uptake is a key feature of UDA ascribed to the highly negatively charged archaeolipids of the TPL, which are recognized by a receptor specialized in uptake and not involved in downstream signaling. Despite dsLp alone was also immunostimulatory on J774A1 cells, applied twice a week on consecutive days along 7 weeks on Balb/c mice, it raised no measurable response unless associated to UDL or UDA. The highest systemic response, IgGa2 mediated, 1 log lower than im dsLp Al2O3, was elicited by dsLp-UDA. Such findings suggest that in vivo, UDL and UDA acted as penetration enhancers for dsLp, but only dsLp-UDA, owed to its pronounced uptake by APC, succeeded as topical adjuvants. The actual TPL composition, fully made of sn2,3 ether linked saturated archaeolipids, gives the UDA bilayer resistance against chemical, physical and enzymatic attacks that destroy ordinary phospholipids bilayers. Together, these properties make UDA a promising platform for topical drug targeted delivery and vaccination, that may be of help for countries with a deficient healthcare system.

摘要

用胆酸钠溶解的巴西利什曼原虫前鞭毛体的总抗原(dsLp),被制备成超可变形纳米囊泡(dsLp-超可变形古脂质体,(dsLp-UDA)和dsLp-超可变形脂质体(dsLp-UDL)),并局部施用于Balb/c小鼠。超可变形纳米囊泡可以穿透完整的角质层直至活表皮,无需借助可能损害皮肤屏障功能的传统渗透促进剂。简要地说,制备了具有-31.45 mV Z电位、含4.84±0.53%w/w蛋白质/脂质dsLp、杨氏模量为235 KPa的100 nm单层dsLp-UDA(大豆磷脂酰胆碱:嗜盐碱红菌总极性脂质(TPL):胆酸钠,3:3:1 w:w)。在体外,dsLp-UDA被J774A1细胞和骨髓来源细胞大量摄取,并且是唯一能诱导J774A1细胞立即分泌IL-6、IL-12p40和TNF-α,随后分泌IL-1β的物质。这种大量摄取是UDA的一个关键特征,这归因于TPL中高度带负电荷的古脂质,它们被专门用于摄取的受体识别且不参与下游信号传导。尽管单独的dsLp对J774A1细胞也有免疫刺激作用,但在Balb/c小鼠上连续7周每周两次应用时,除非与UDL或UDA联合使用,否则不会引起可测量的反应。dsLp-UDA引发了最高的全身反应,由IgGa2介导,比肌肉注射dsLp Al2O3低1个对数。这些发现表明,在体内,UDL和UDA作为dsLp的渗透促进剂,但只有dsLp-UDA由于其被抗原呈递细胞显著摄取,成功地作为局部佐剂。实际的TPL组成完全由sn2,3醚键连接的饱和古脂质构成,赋予UDA双层抵抗破坏普通磷脂双层的化学、物理和酶攻击的能力。总之,这些特性使UDA成为局部药物靶向递送和疫苗接种的一个有前景的平台,这可能对医疗保健系统不完善的国家有所帮助。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5013/4774928/23e387091860/pone.0150185.g001.jpg

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