Calvo-Serrano Silvia, Matamoros Esther, Céspedes Jose Antonio, Fernández-Santamaría Rubén, Gil-Ocaña Violeta, Perez-Inestrosa Ezequiel, Frecha Cecilia, Montañez Maria I, Vida Yolanda, Mayorga Cristobalina, Torres Maria J
Allergy Research Group, Instituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina-IBIMA Plataforma Bionand, Parque Tecnológico de Andalucía, 29590 Málaga, Spain.
RICORS Red de Enfermedades Inflamatorias (REI), 28029 Madrid, Spain.
Pharmaceutics. 2024 Aug 3;16(8):1039. doi: 10.3390/pharmaceutics16081039.
In vitro cell activation through specific IgE bound to high-affinity receptors on the basophil surface is a widely used strategy for the evaluation of IgE-mediated immediate hypersensitivity reactions to betalactams. Cellular activation requires drug conjugation to a protein to form a large enough structure displaying a certain distance between haptens to allow the cross-linking of two IgE antibodies bound to the basophil's surface, triggering their degranulation. However, no information about the size and composition of these conjugates is available. Routine in vitro diagnosis using the basophil activation test uses free amoxicillin, which is assumed to conjugate to a carrier present in blood. To standardize the methodology, we propose the use of well-controlled and defined nanomaterials functionalized with amoxicilloyl. Silica nanoparticles decorated with PAMAM-dendrimer-amoxicilloyl conjugates (NpDeAXO) of different sizes and amoxicilloyl densities (50-300 µmol amoxicilloyl/gram nanoparticle) have been prepared and chemically characterized. Two methods of synthesis were performed to ensure reproducibility and stability. Their functional effect on basophils was measured using an basophil activation test (BAT) that determines CD63 or CD203c activation markers. It was observed that NpDeAXO nanocomposites are not only able to specifically activate basophils but also do so in a more effective way than free amoxicillin, pointing to a translational potential diagnosis.
通过结合在嗜碱性粒细胞表面高亲和力受体上的特异性IgE进行体外细胞激活,是评估IgE介导的对β-内酰胺类药物速发型超敏反应的一种广泛应用的策略。细胞激活需要将药物与蛋白质偶联,以形成足够大的结构,使半抗原之间保持一定距离,从而使结合在嗜碱性粒细胞表面的两种IgE抗体发生交联,触发其脱颗粒。然而,关于这些偶联物的大小和组成尚无相关信息。使用嗜碱性粒细胞激活试验的常规体外诊断采用游离阿莫西林,假定它与血液中存在的载体偶联。为了使方法标准化,我们建议使用经阿莫西林酰基功能化的、控制良好且定义明确的纳米材料。已制备了不同尺寸和阿莫西林酰基密度(50 - 300 μmol阿莫西林酰基/克纳米颗粒)的、用PAMAM - 树枝状大分子 - 阿莫西林酰基偶联物修饰的二氧化硅纳米颗粒(NpDeAXO),并对其进行了化学表征。进行了两种合成方法以确保可重复性和稳定性。使用测定CD63或CD203c激活标志物的嗜碱性粒细胞激活试验(BAT)来测量它们对嗜碱性粒细胞的功能作用。观察到NpDeAXO纳米复合材料不仅能够特异性激活嗜碱性粒细胞,而且比游离阿莫西林更有效,具有潜在的转化诊断价值。