Cytokine Profile Response of Human Peripheral Blood Mononuclear Cells Stimulated by Bartonella bacilliformis.

IF 1.9 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Interferon and Cytokine Research Pub Date : 2024-01-01 Epub Date: 2023-11-15 DOI:10.1089/jir.2023.0107
Barbara Ymaña, Javier Enciso-Benavides, Gemma Moncunill, Maria J Pons
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Abstract

Carrion's disease is a neglected endemic disease found in remote Andean areas. As an overlooked disease, knowledge of innate immune responses to Bartonella bacilliformis, the etiological agent, is scarce. This study aimed to evaluate the cytokine response to B. bacilliformis using in vitro human peripheral blood mononuclear cells (PBMCs) stimulations. PBMCs from naive adults were isolated by gradient centrifugation and cocultured with heat-inactivated (HI) B. bacilliformis at different incubation times (3, 6, 12, 24, and 36 h). Cytokines, chemokines, and growth factors were determined in culture supernatants by multiplex fluorescent bead-based quantitative suspension array technology. During the first 36 h, a proinflammatory response was observed, including tumor necrosis factor-α, interleukin (IL)-1α, IL-1β, interferon-α2, and IL-6, followed by an anti-inflammatory response mainly related to IL-1RA. Moreover, high expression levels of chemokines IL-8, monocyte chemoattractant protein-1α, and macrophage inflammatory protein (MIP)-1β were detected from 3 h poststimulation and MIP-1α was detected at 24 h. Some growth factors, mainly granulocyte macrophage colony-stimulating factor and granulocyte colony-stimulating factor, and in minor concentrations vascular endothelial growth factor, epidermal growth factor, and eotaxin, were also detected. Innate response to HI B. bacilliformis stimulation consists of a rapid and strong proinflammatory response characterized by a wide range of cytokines and chemokines followed by an anti-inflammatory response and increased specific growth factors.

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杆菌状巴尔通体刺激人外周血单个核细胞的细胞因子谱反应。
腐肉病是一种被忽视的地方病,常见于偏远的安第斯地区。作为一种被忽视的疾病,对病原体巴通体杆菌的先天免疫反应的了解很少。本研究旨在通过体外刺激人外周血单个核细胞(PBMCs)来评估细胞因子对芽孢杆菌的反应。通过梯度离心分离初生成人的pbmc,并在不同孵育时间(3,6,12,24和36 h)与热灭活(HI)芽孢杆菌共培养。细胞因子、趋化因子和生长因子通过基于多重荧光珠的定量悬浮阵列技术在培养上清液中进行检测。在前36小时,观察到促炎反应,包括肿瘤坏死因子-α、白细胞介素(IL)-1α、IL-1β、干扰素-α2和IL-6,随后是主要与IL- 1ra相关的抗炎反应。此外,趋化因子IL-8、单核细胞趋化蛋白-1α和巨噬细胞炎症蛋白(MIP)-1β在刺激后3小时高表达,MIP-1α在24小时高表达。部分生长因子,主要是粒细胞巨噬细胞集落刺激因子和粒细胞集落刺激因子,以及少量浓度的血管内皮生长因子、表皮生长因子和eotaxin。对HI芽孢杆菌刺激的先天反应包括快速而强烈的促炎反应,其特征是广泛的细胞因子和趋化因子,随后是抗炎反应和特异性生长因子的增加。
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来源期刊
CiteScore
3.80
自引率
0.00%
发文量
78
审稿时长
2.2 months
期刊介绍: Journal of Interferon & Cytokine Research (JICR) provides the latest groundbreaking research on all aspects of IFNs and cytokines. The Journal delivers current findings on emerging topics in this niche community, including the role of IFNs in the therapy of diseases such as multiple sclerosis, the understanding of the third class of IFNs, and the identification and function of IFN-inducible genes.
期刊最新文献
A Conversation with Professor Susan Kaech. Experts Speak: A Conversation with Professor Stefan Rose-John. Experts Speak: A Conversation with Professor Laura Mackay. Alternative Splicing of RNA Is Excessive in Multiple Sclerosis and Not Linked to Gene Expression Levels: Dysregulation Is Corrected by IFN-β. Alternative Splicing in Multiple Sclerosis: A Promising Biomarker of Therapeutic Response to Interferon-β.
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