Roe Emily F, Freire Haddad Helena, Lazar Kat M, Liu Peiying, Collier Joel H
Department of Biomedical Engineering, Duke University, Durham, NC, 27708, USA.
Adv Healthc Mater. 2025 Jan;14(3):e2402055. doi: 10.1002/adhm.202402055. Epub 2024 Dec 15.
Mucosal immune responses to vaccination are essential for achieving full protection against pathogens entering their host at mucosal sites. However, traditional parenteral immunization routes commonly fail to raise significant mucosal immunity. Sublingual immunization is a promising alternative delivery route to raise robust immune responses both systemically and at mucosal sites, and nanomaterial-based subunit vaccine platforms offer opportunities for raising epitope-specific responses. Here, sublingual immunization is reported using the Coil29 platform of coiled-coil self-assembling peptide nanofibers. The successful immunization with epitopes of varying physicochemical properties by including mucus-modulating components - namely sequences of proline, alanine, and serine (PAS) is demonstrated. PASylation is shown to decrease mucin complexation and increase epithelial penetration in vitro, enabling sublingual immunization against a variety of selected peptide epitopes in vivo. Coil29 fibers are also readily formed into tablets for solid-state dosing formulations and maintain their immunogenicity in this state. Previous sublingual peptide nanofiber immunotherapies have been based on different structures, such as highly stable β-sheets. The present work demonstrates that alternatively folded structures such as α-helical nanofibers can also be rendered sublingually immunogenic, enabling immunization with a variety of peptide epitopes and offering additional ways to specify mucus interactions, delivery state, dosing, and formulation.
对疫苗接种产生黏膜免疫反应对于实现对在黏膜部位进入宿主的病原体的全面保护至关重要。然而,传统的肠胃外免疫途径通常无法引发显著的黏膜免疫。舌下免疫是一种有前景的替代给药途径,可在全身和黏膜部位引发强大的免疫反应,基于纳米材料的亚单位疫苗平台为引发表位特异性反应提供了机会。在此,报道了使用卷曲螺旋自组装肽纳米纤维的Coil29平台进行舌下免疫。通过包含黏液调节成分——即脯氨酸、丙氨酸和丝氨酸(PAS)序列,证明了对具有不同物理化学性质的表位进行成功免疫。PAS化在体外显示可减少黏蛋白络合并增加上皮穿透,从而能够在体内针对多种选定的肽表位进行舌下免疫。Coil29纤维也很容易制成片剂用于固态给药制剂,并在此状态下保持其免疫原性。先前的舌下肽纳米纤维免疫疗法基于不同的结构,如高度稳定的β-折叠片。目前的工作表明,诸如α-螺旋纳米纤维等交替折叠结构也可具有舌下免疫原性,从而能够用多种肽表位进行免疫,并提供了指定黏液相互作用、给药状态、剂量和制剂的额外方法。