Gnosis by Lesaffre - Research & Applications department, Lesaffre Group, Marcq-en-Baroeul, France.
NIZO, Ede, the Netherlands.
Benef Microbes. 2024 Aug 14;15(6):659-678. doi: 10.1163/18762891-bja00028.
LifeinU™ Bacillus subtilis CU1 (BSCU1) has been previously shown to be effective in stimulating mucosal immune responses and supporting resistance to common infectious disease episodes in the elderly. The current clinical study aimed at exploring potential pathways by which BSCU1 could beneficially modulate the immune system and contribute to protection against infection in the general population. A total of 88 participants from three different age groups were supplemented with BSCU1 (2 × 109 cfu/day) for 4 weeks. The effect of the intervention on mucosal immunity was assessed by faecal sIgA levels. In addition, a series of complementary immunoassays were selected, including immune phenotyping, gene expression, basal cytokine levels, cytokine levels in lipopolysaccharide (LPS)-stimulated whole blood and phagocytosis assay. Although no significant effect was observed on faecal sIgA levels after intervention, BSCU1 showed a positive effect on a consistent set of markers of the peripheral innate immune system in adults and the elderly. Percentages of peripheral blood myeloid cells as well as the expression of the activation marker CD69 on monocytes were significantly increased after probiotic intervention. BSCU1 supplementation resulted in significant enrichment of clusters of genes involved in response to type I interferon and phagocytosis pathway. Consistently, ex vivo stimulation of whole blood with LPS resulted in a statistically significant increase in pro-inflammatory cytokines (interleukin (IL)-1beta, IL-6, interferon-gamma, IL-12, tumour necrosis factor (TNF)-alpha, macrophage inflammatory protein (MIP)-1alpha, IL-8) and phagocytosis assays showed increased capacity of monocytes to engulf bacteria as well as higher phagosome maturation. BSCU1 supplementation also had a positive effect on low-grade inflammation as significant reduction in basal levels of several serum cytokines (IL-10, TNF-alpha, MIP-1alpha, IL-8) were observed in the elderly subgroup. Overall, BSCU1 primed immune cells for a better response to microbial challenges and reduced low-grade inflammation associated with aging. Registered at ClinicalTrials.gov with the identifier NCT05403398.
U 型生活®枯草芽孢杆菌 CU1(BSCU1)先前已被证明可有效刺激黏膜免疫反应,并支持老年人抵抗常见传染病发作。目前的临床研究旨在探索 BSCU1 可能通过有益地调节免疫系统并有助于保护普通人群免受感染的潜在途径。共有来自三个不同年龄组的 88 名参与者每天补充 BSCU1(2×109 cfu)4 周。通过粪便 sIgA 水平评估干预对黏膜免疫的影响。此外,选择了一系列互补免疫测定法,包括免疫表型、基因表达、基础细胞因子水平、脂多糖(LPS)刺激全血中的细胞因子水平和吞噬作用测定法。尽管干预后粪便 sIgA 水平没有明显变化,但 BSCU1 对成人和老年人外周固有免疫系统的一组一致标志物显示出积极影响。外周血髓样细胞的百分比以及单核细胞激活标志物 CD69 的表达在益生菌干预后显著增加。BSCU1 补充导致参与 I 型干扰素反应和吞噬作用途径的基因簇显著富集。一致地,用 LPS 对全血进行体外刺激导致促炎细胞因子(白细胞介素(IL)-1β、IL-6、干扰素-γ、IL-12、肿瘤坏死因子(TNF)-α、巨噬细胞炎症蛋白(MIP)-1α、IL-8)的统计学显着增加,吞噬作用测定法显示单核细胞吞噬细菌的能力增加,吞噬体成熟度更高。BSCU1 补充对低度炎症也有积极影响,因为在老年亚组中观察到几种血清细胞因子(IL-10、TNF-α、MIP-1α、IL-8)的基础水平显着降低。总的来说,BSCU1 为免疫细胞对微生物挑战做出更好的反应做好了准备,并减少了与衰老相关的低度炎症。在 ClinicalTrials.gov 上以标识符 NCT05403398 注册。