Electrochemical Cytokine Profiling Reveals Dual Immunomodulatory Effects of Human Milk Oligosaccharides in THP-1 Macrophages

IF 4.5 2区 医学 Q2 CHEMISTRY, MEDICINAL
ACS Infectious Diseases Pub Date : 2026-10-09 Epub Date: 2026-09-30 DOI:10.1021/acsinfecdis.6c00388
Victoria A. Federico, Hannah A. Richards, Julie A. Talbert, Jocelyn R. Leal, Jennifer A. Gaddy, Steven D. Townsend, David E. Cliffel
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引用次数: 0

Abstract

Human milk oligosaccharides (HMOs) are bioactive carbohydrates that govern host–microbe interactions and immune regulation. Beyond their antimicrobial and antibiofilm functions, HMOs have been shown to modulate inflammatory pathways by altering cytokine expression, including interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α), which are key mediators in infection and inflammation associated complications. In this study, we characterize the effects of HMOs on cytokine secretion in THP-1 macrophages stimulated with lipopolysaccharides using a validated magnetic bead electrochemical sandwich assay (MBESA). The electrochemical assay enabled precise quantification of cytokine responses and revealed that HMO treatment attenuated proinflammatory signaling in LPS stimulated macrophages. These findings provide new insights into the immunomodulatory properties of HMOs and demonstrate the utility of electrochemical biosensing platforms for rapid, sensitive assessment of cellular inflammatory responses. Future studies will expand this approach to microphysiological systems to further elucidate HMO mediated regulation of immune signaling.

电化学细胞因子谱揭示人乳寡糖对THP-1巨噬细胞的双重免疫调节作用
人乳寡糖(HMOs)是一种生物活性碳水化合物,可调节宿主与微生物的相互作用和免疫调节。除了抗菌和抗生物膜功能外,HMOs还通过改变细胞因子的表达来调节炎症途径,包括白细胞介素-1β (IL-1β)和肿瘤坏死因子-α(TNF-α),它们是感染和炎症相关并发症的关键介质。在本研究中,我们利用已验证的磁珠电化学夹心法(MBESA)表征了HMOs对脂多糖刺激的THP-1巨噬细胞细胞因子分泌的影响。电化学分析能够精确量化细胞因子反应,并揭示HMO治疗可以减弱LPS刺激的巨噬细胞中的促炎信号。这些发现为HMOs的免疫调节特性提供了新的见解,并证明了电化学生物传感平台在快速、敏感地评估细胞炎症反应方面的实用性。未来的研究将把这一方法扩展到微生理系统,以进一步阐明HMO介导的免疫信号调节。
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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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