Colaço Mariana, Cruz Maria T, Almeida Luís Pereira de, Borges Olga
CNC-UC-Center for Neuroscience and Cell Biology, University of Coimbra, 3004-504 Coimbra, Portugal.
CIBB-Center for Innovative Biomedicine and Biotechnology, University of Coimbra, 3004-504 Coimbra, Portugal.
Pharmaceutics. 2024 Oct 8;16(10):1308. doi: 10.3390/pharmaceutics16101308.
BACKGROUND/OBJECTIVES: Nasal vaccines are a promising strategy for enhancing mucosal immune responses and preventing diseases at mucosal sites by stimulating the secretion of secretory IgA, which is crucial for early pathogen neutralization. However, designing effective nasal vaccines is challenging due to the complex immunological mechanisms in the nasal mucosa, which must balance protection and tolerance against constant exposure to inhaled pathogens. The nasal route also presents unique formulation and delivery hurdles, such as the mucous layer hindering antigen penetration and immune cell access.
This review focuses on cutting-edge approaches to enhance nasal vaccine delivery, particularly those targeting C-type lectin receptors (CLRs) like the mannose receptor and macrophage galactose-type lectin (MGL) receptor. It elucidates the roles of these receptors in antigen recognition and uptake by antigen-presenting cells (APCs), providing insights into optimizing vaccine delivery.
While a comprehensive examination of targeted glycoconjugate vaccine development is outside the scope of this study, we provide key examples of glycan-based ligands, such as lactobionic acid and mannose, which can selectively target CLRs in the nasal mucosa.
With the rise of new viral infections, this review aims to facilitate the design of innovative vaccines and equip researchers, clinicians, and vaccine developers with the knowledge to enhance immune defenses against respiratory pathogens, ultimately protecting public health.
背景/目的:鼻用疫苗是一种很有前景的策略,可通过刺激分泌型IgA的分泌来增强黏膜免疫反应并预防黏膜部位的疾病,而分泌型IgA对于早期病原体中和至关重要。然而,设计有效的鼻用疫苗具有挑战性,因为鼻黏膜中的免疫机制复杂,必须在针对持续吸入病原体的保护和耐受之间取得平衡。鼻内给药途径还存在独特的制剂和给药障碍,例如黏液层会阻碍抗原渗透和免疫细胞进入。
本综述重点关注增强鼻用疫苗递送的前沿方法,特别是那些针对甘露糖受体和巨噬细胞半乳糖型凝集素(MGL)受体等C型凝集素受体(CLR)的方法。它阐明了这些受体在抗原呈递细胞(APC)对抗原的识别和摄取中的作用,为优化疫苗递送提供了见解。
虽然对靶向糖缀合物疫苗开发的全面研究超出了本研究的范围,但我们提供了基于聚糖的配体的关键实例,如乳糖酸和甘露糖,它们可以选择性地靶向鼻黏膜中的CLR。
随着新的病毒感染的增加,本综述旨在促进创新疫苗的设计,并为研究人员、临床医生和疫苗开发者提供知识,以增强对呼吸道病原体的免疫防御,最终保护公众健康。