Department of Immunology, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Cellular and Molecular Research Center, Research Institute for Prevention of Non-communicable Disease, Qazvin University of Medical Sciences, Qazvin, Iran.
Int Immunopharmacol. 2021 Dec;101(Pt B):108350. doi: 10.1016/j.intimp.2021.108350. Epub 2021 Nov 12.
Allergen-specific sublingual immunotherapy (SLIT), a safe and efficient route for treating type I hypersensitivity disorders, requires high doses of allergens. SLIT is generally performed without adjuvants and delivery systems. Therefore, allergen formulation with appropriate presentation platforms results in improved allergen availability, targeting the immune cells, inducing regulatory immune responses, and enhancing immunotherapy's efficacy while decreasing the dose of the allergen. In this review, we discuss the adjuvants and delivery systems that have been applied as allergen-presentation platforms for SLIT. These adjuvants include TLRs ligands, 1α, 25-dihydroxy vitamin D3, galectin-9, probiotic and bacterial components that provoke allergen-specific helper type-1 T lymphocytes (TH1), and regulatory T cells (Tregs). Another approach is encapsulation or adsorption of the allergens into a particulate vector system to facilitate allergen capture by tolerogenic dendritic cells. Also, we proposed strategies to increasing the efficacy of SLIT via new immunopotentiators and carrier systems in the future.
变应原特异性舌下免疫疗法 (SLIT) 是一种治疗 I 型超敏反应疾病的安全有效的方法,需要高剂量的变应原。SLIT 通常在没有佐剂和给药系统的情况下进行。因此,具有适当递呈平台的变应原配方可提高变应原的可用性,靶向免疫细胞,诱导调节性免疫反应,并增强免疫疗法的疗效,同时降低变应原的剂量。在这篇综述中,我们讨论了已被用作 SLIT 变应原递呈平台的佐剂和给药系统。这些佐剂包括 TLR 配体、1α, 25-二羟维生素 D3、半乳糖凝集素-9、益生菌和细菌成分,它们可引发变应原特异性辅助型 1 T 淋巴细胞 (TH1) 和调节性 T 细胞 (Tregs)。另一种方法是将过敏原包封或吸附到颗粒载体系统中,以促进耐受性树突状细胞捕获过敏原。此外,我们还提出了通过新的免疫增强剂和载体系统在未来提高 SLIT 疗效的策略。