适体
超抗原
促炎细胞因子
T细胞
肠毒素
化学
流式细胞术
单克隆抗体
分子生物学
体外
免疫系统
微生物学
细胞生物学
免疫学
生物
抗体
炎症
生物化学
大肠杆菌
基因
作者
Leslie Chávez‐Galán,Andy Ruíz,Lucero A. Ramón‐Luing,Alejandro Escamilla-Gutiérrez,Anahí Sánchez-Monciváis,Brenda Tecuatzi-Cadena,Karen Medina-Quero,María Guadalupe Córdova-Espinoza
出处
期刊:Molecules
[MDPI AG]
日期:2023-04-14
卷期号:28 (8): 3480-3480
被引量:1
标识
DOI:10.3390/molecules28083480
摘要
Staphylococcal enterotoxin B (SEB) is a protein produced by Staphylococcus aureus, which is toxic to humans. It is well known for its ability to stimulate the exacerbated activation of proinflammatory CD4+ T cells (Th1 profile), and in vitro studies have been conducted to understand its mechanism of action and its potential use as an immune therapy. However, the efficiency of the SEB1741 aptamer in blocking SEB has not been experimentally demonstrated.Enrichment CD4+ T cells were stimulated with SEB, and as a blocker, we used the SEB1741 aptamer, which was previously synthesised by an "in silico" analysis, showing high affinity and specificity to SEB. The efficiency of the SEB1741 aptamer in blocking CD4+ T cell activation was compared with that of an anti-SEB monoclonal antibody. Flow cytometry and Bio-Plex were used to evaluate the T-cell function.In vitro, SEB induced the activation of CD4+ T cells and favoured a Th1 profile; however, the SEB1741 aptamer was highly efficient in decreasing the frequency of CD4+ T cells positive to ki-67 and CD69 cells, this means that proliferation and activation of CD4+ T cells was decreased. Moreover, the production of interleukin 2 (IL-2) and interferon-gamma (IFN-γ) was affected, suggesting that the Th1 profile is not present when the SEB1441 aptamer is used. Thus, the SEB1741 function was similar to that of anti-SEB.The SEB1741 aptamer is a valuable tool for blocking CD4+ T cell activation and the subsequent release of proinflammatory cytokines by SEB stimulation.
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