Mone Kiruthiga, Singh Shraddha, Abdullatif Fatema, Sur Meghna, Rasquinha Mahima T, Seravalli Javier, Zinniel Denise K, Mukhopadhyay Indranil, Barletta Raul G, Gebregiworgis Teklab, Reddy Jay
School of Veterinary Medicine and Biomedical Sciences, University of Nebraska-Lincoln, Lincoln, NE 68583, USA.
Department of Biochemistry, Schulich School of Medicine and Dentistry, University of Western Ontario, London, ON N6A 5C1, Canada.
Vaccines (Basel). 2025 Jul 21;13(7):768. doi: 10.3390/vaccines13070768.
BACKGROUND/OBJECTIVES: Freund's adjuvants induce different immunomodulatory effects, but their underlying molecular mechanisms are unclear. In this study, we investigated whether the immune-stimulating effects of the complete Freund's adjuvant (CFA) involve the mechanisms of trained immunity (TI).
We examined bone marrow cells (BMCs) isolated from CFA-immunized A/J mice to address this question. Incomplete Freund's adjuvant (IFA) and var. Bacillus Calmette-Guérin (BCG) served as negative and positive controls, respectively. We evaluated cytokine profiles, metabolic, and epigenetic changes.
First, BMCs from all groups except saline showed varied levels of IL-1β, IL-6, and TNF-α. But expression of CCL5 and CXCL10 was significantly elevated only in the CFA and BCG groups. Transcriptionally, significant elevations were noted for TNF-α and IL-1β in the CFA and BCG groups, whereas CXCL10, IL-6, and IL-10 were upregulated in the CFA and BCG groups, respectively. Second, while BMCs from the BCG group expressed the markers of both the M1 and M2 macrophages, no clear trends were noted in the CFA and IFA groups. Third, cell lysates from the CFA group revealed metabolic reprogramming in the BMCs. Specifically, we observed an increased level of lactate, indicative of aerobic glycolysis, which is implicated in TI, and this was also detected in the IFA group. Fourth, epigenetic analysis revealed histone enrichment in the promoter region of TNF-α, in the CFA group, but to a lesser degree than the BCG group. However, no epigenetic changes were observed in the IFA group.
Our data provide new insights into the mechanisms of Freund's adjuvants and the immunomodulatory effects of CFA could involve the features of TI.
背景/目的:弗氏佐剂可诱导不同的免疫调节作用,但其潜在的分子机制尚不清楚。在本研究中,我们调查了完全弗氏佐剂(CFA)的免疫刺激作用是否涉及训练免疫(TI)机制。
为解决这个问题,我们检测了从接受CFA免疫的A/J小鼠中分离出的骨髓细胞(BMC)。不完全弗氏佐剂(IFA)和卡介苗(BCG)分别作为阴性和阳性对照。我们评估了细胞因子谱、代谢和表观遗传变化。
首先,除生理盐水组外,所有组的BMC中白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)水平各不相同。但趋化因子配体5(CCL5)和CXC趋化因子配体10(CXCL10)的表达仅在CFA组和BCG组显著升高。在转录水平上,CFA组和BCG组的TNF-α和IL-1β显著升高,而CXCL10、IL-6和白细胞介素-10(IL-10)分别在CFA组和BCG组中上调。其次,虽然BCG组的BMC表达了M1和M2巨噬细胞的标志物,但CFA组和IFA组未观察到明显趋势。第三,CFA组的细胞裂解物显示BMC中存在代谢重编程。具体而言,我们观察到乳酸水平升高,这表明有氧糖酵解增加,这与TI有关,并且在IFA组中也检测到了这一点。第四,表观遗传分析显示,CFA组中TNF-α启动子区域存在组蛋白富集,但程度低于BCG组。然而,IFA组未观察到表观遗传变化。
我们的数据为弗氏佐剂的机制提供了新的见解,CFA的免疫调节作用可能涉及TI的特征。