Department of Immunology and Infectious Biology, Institute of Microbiology, Biotechnology and Immunology, Faculty of Biology and Environmental Protection, University of Lodz, Banacha 12/16, 90-237, Lodz, Poland.
Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Sienkiewicza 112, 90-636, Lodz, Poland.
Sci Rep. 2024 Feb 27;14(1):4747. doi: 10.1038/s41598-024-55353-6.
Gram-negative spiral-shaped Helicobacter pylori (Hp) bacteria induce the development of different gastric disorders. The growing resistance of Hp to antibiotics prompts to search for new therapeutic formulations. A promising candidate is Mycobacterium bovis BCG (BCG) with immunomodulatory properties. Biodegradable mucoadhesive chitosan is a good carrier for delivering BCG mycobacteria to the gastric mucosal environment. This study aimed to show whether BCG bacilli are able to increase the phagocytic activity of Cavia porcellus-guinea pig macrophages derived from the bone marrow towards fluorescently labeled Escherichia coli. Furthermore, to encapsulate live BCG bacilli, in spray-dried chitosan microparticles (CHI-MPs), and assess the pH-dependent release of mycobacteria in pH conditions mimicking gastric (acidic) or gut (alkaline) milieu. Microparticles (MPs) were made of chitosan and coated with Pluronic F-127-(Plur) or N-Acetyl-D-Glucosamine-(GlcNAc) to increase the MPs resistance to low pH or to increase anti-Hp effect, respectively. Spray-drying method was used for microencapsulation of live BCG. The biosafety of tested CHI-MPs has been confirmed using cell models in vitro and the model of guinea pig in vivo. The CHI-MPs loaded with BCG released live mycobacteria at pH 3.0 (CHI-GlcNAc-MPs) or pH 8.0. (CHI-Plur-MPs). The CHI-MPs loaded with live BCG can be used for per os inoculation of Cavia porcellus to check the effectiveness of delivered mycobacteria in increasing anti-H. pylori host response.
革兰氏阴性螺旋形幽门螺杆菌 (Hp) 细菌会引发不同的胃部疾病。Hp 对抗生素的耐药性不断增加,促使人们寻找新的治疗方案。具有免疫调节特性的牛分枝杆菌 BCG(BCG)是一种很有前途的候选药物。可生物降解的黏附性壳聚糖是将 BCG 分枝杆菌递送到胃黏膜环境的良好载体。本研究旨在证明 BCG 杆菌是否能够提高源自豚鼠骨髓的 Cavia porcellus-豚鼠巨噬细胞对荧光标记的大肠杆菌的吞噬活性。此外,要将活的 BCG 杆菌包封在喷雾干燥的壳聚糖微球(CHI-MPs)中,并评估在模拟胃(酸性)或肠道(碱性)环境的 pH 条件下,分枝杆菌的 pH 依赖性释放。微球(MPs)由壳聚糖制成,并涂有 Pluronic F-127-(Plur) 或 N-乙酰-D-氨基葡萄糖(GlcNAc),以分别提高 MPs 对低 pH 的抵抗力或增强抗-Hp 作用。喷雾干燥法用于微封装活的 BCG。使用体外细胞模型和豚鼠体内模型证实了测试用 CHI-MPs 的生物安全性。在 pH 值为 3.0(CHI-GlcNAc-MPs)或 pH 值为 8.0 时,负载 BCG 的 CHI-MPs 会释放出活的分枝杆菌。(CHI-Plur-MPs)。负载活 BCG 的 CHI-MPs 可用于豚鼠口服接种,以检查递送至宿主的分枝杆菌在增强抗-Hp 宿主反应方面的有效性。