Stella Cochrane, Ramya Rajagopal, David Sheffield, Fay Stewart, Lindsay Hathaway, Nicholas M Barnes, Omar Qureshi, John Gordon
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In addition to results on the impact of the stimuli used, initial profiling data for a case study chemical, curcumin, is presented, illustrating how the system can be used to generate information on the impact of exogenous materials on three major constituent immune cell subsets for use in risk assessment and to direct follow-on studies. <b>Results:</b> The different stimuli drove distinct responses, not only in relation to the \"quantity\" of the response but also the \"quality\". Curcumin had a limited impact on the B cell parameters measured, with the stimuli used, and it was noted that in contrast to T cells where there was either no impact or a reduction in viability and proliferation with increasing concentration, for B cells there was a small but significant increase in both measurements at curcumin concentrations below 20 µM. Similarly, whilst expression of activation markers by T cells was reduced by the highest concentration of curcumin, they were increased in B cells. Curcumin only impacted the viability of stimulated monocytes at the highest concentration and had differential impact on different activation markers. Levels of all cytokines and PGE2 were reduced at higher concentrations. <b>Discussion:</b> Although the platform has certain limitations, it nevertheless enables assessment of healthy baseline monocyte, T-, and B-cell responses, and scrutiny of the impact of different stimuli to detect potential immune suppression or enhancement from exogenous materials. In the case of curcumin, a pattern of responses indicative of immune suppressive / anti-inflammatory effects was detected. It is an accessible, highly modifiable system that can be used to screen materials and guide further studies, providing a holistic, integrated picture of effects.</p>","PeriodicalId":73111,"journal":{"name":"Frontiers in toxicology","volume":"6 ","pages":"1335110"},"PeriodicalIF":3.6000,"publicationDate":"2024-04-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11082367/pdf/","citationCount":"0","resultStr":"{\"title\":\"Impact of a varied set of stimuli on a suite of immunological parameters within peripheral blood mononuclear cells: toward a non-animal approach for assessing immune modulation by materials intended for human use.\",\"authors\":\"Stella Cochrane, Ramya Rajagopal, David Sheffield, Fay Stewart, Lindsay Hathaway, Nicholas M Barnes, Omar Qureshi, John Gordon\",\"doi\":\"10.3389/ftox.2024.1335110\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Introduction:</b> In toxicology, steps are being taken towards more mechanism-focused and human relevant approaches to risk assessment, requiring new approaches and methods. Additionally, there is increasing emphasis by regulators on risk assessment of immunotoxicity. <b>Methods:</b> Here we present data from a peripheral blood mononuclear cell (PBMC) system whereby a varied set of stimuli, including those against the TCR and Toll-like receptors, enable readouts of cytokine and prostaglandin E2 (PGE2) production with monocyte, T cell and B cell viability, proliferation, and associated activation markers. In addition to results on the impact of the stimuli used, initial profiling data for a case study chemical, curcumin, is presented, illustrating how the system can be used to generate information on the impact of exogenous materials on three major constituent immune cell subsets for use in risk assessment and to direct follow-on studies. <b>Results:</b> The different stimuli drove distinct responses, not only in relation to the \\\"quantity\\\" of the response but also the \\\"quality\\\". Curcumin had a limited impact on the B cell parameters measured, with the stimuli used, and it was noted that in contrast to T cells where there was either no impact or a reduction in viability and proliferation with increasing concentration, for B cells there was a small but significant increase in both measurements at curcumin concentrations below 20 µM. Similarly, whilst expression of activation markers by T cells was reduced by the highest concentration of curcumin, they were increased in B cells. Curcumin only impacted the viability of stimulated monocytes at the highest concentration and had differential impact on different activation markers. Levels of all cytokines and PGE2 were reduced at higher concentrations. <b>Discussion:</b> Although the platform has certain limitations, it nevertheless enables assessment of healthy baseline monocyte, T-, and B-cell responses, and scrutiny of the impact of different stimuli to detect potential immune suppression or enhancement from exogenous materials. In the case of curcumin, a pattern of responses indicative of immune suppressive / anti-inflammatory effects was detected. 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引用次数: 0
摘要
导言:在毒理学领域,人们正在采取措施,采用更加注重机理和与人类相关的方法来进行风险评估,这就需要采用新的方法和手段。此外,监管机构也越来越重视免疫毒性的风险评估。方法:在这里,我们展示了外周血单核细胞(PBMC)系统的数据,通过该系统可读出细胞因子和前列腺素 E2(PGE2)的产生情况,以及单核细胞、T 细胞和 B 细胞的活力、增殖和相关活化标记。除了所使用的刺激物的影响结果外,还介绍了案例研究化学品姜黄素的初步分析数据,说明了该系统如何用于生成外源材料对三个主要免疫细胞亚群的影响信息,以用于风险评估和指导后续研究。结果:不同的刺激不仅在反应的 "量 "方面,而且在 "质 "方面都产生了不同的反应。姜黄素对所测量的 B 细胞参数的影响有限,所使用的刺激物也是如此。与 T 细胞不受影响或活力和增殖随浓度增加而减少的情况不同,姜黄素浓度低于 20 µM 时,B 细胞的活力和增殖都有小幅但显著的增加。同样,虽然姜黄素的最高浓度降低了 T 细胞活化标志物的表达,但 B 细胞的活化标志物表达却增加了。姜黄素只在最高浓度时才会影响受刺激单核细胞的活力,并对不同的活化标志物产生不同的影响。高浓度姜黄素会降低所有细胞因子和 PGE2 的水平。讨论:虽然该平台有一定的局限性,但它仍能评估健康基线单核细胞、T 细胞和 B 细胞的反应,并仔细检查不同刺激的影响,以检测外源物质可能产生的免疫抑制或增强作用。就姜黄素而言,检测到了表明免疫抑制/抗炎作用的反应模式。这是一个易于使用、高度可修改的系统,可用于筛选材料和指导进一步研究,提供全面、综合的效果图谱。
Impact of a varied set of stimuli on a suite of immunological parameters within peripheral blood mononuclear cells: toward a non-animal approach for assessing immune modulation by materials intended for human use.
Introduction: In toxicology, steps are being taken towards more mechanism-focused and human relevant approaches to risk assessment, requiring new approaches and methods. Additionally, there is increasing emphasis by regulators on risk assessment of immunotoxicity. Methods: Here we present data from a peripheral blood mononuclear cell (PBMC) system whereby a varied set of stimuli, including those against the TCR and Toll-like receptors, enable readouts of cytokine and prostaglandin E2 (PGE2) production with monocyte, T cell and B cell viability, proliferation, and associated activation markers. In addition to results on the impact of the stimuli used, initial profiling data for a case study chemical, curcumin, is presented, illustrating how the system can be used to generate information on the impact of exogenous materials on three major constituent immune cell subsets for use in risk assessment and to direct follow-on studies. Results: The different stimuli drove distinct responses, not only in relation to the "quantity" of the response but also the "quality". Curcumin had a limited impact on the B cell parameters measured, with the stimuli used, and it was noted that in contrast to T cells where there was either no impact or a reduction in viability and proliferation with increasing concentration, for B cells there was a small but significant increase in both measurements at curcumin concentrations below 20 µM. Similarly, whilst expression of activation markers by T cells was reduced by the highest concentration of curcumin, they were increased in B cells. Curcumin only impacted the viability of stimulated monocytes at the highest concentration and had differential impact on different activation markers. Levels of all cytokines and PGE2 were reduced at higher concentrations. Discussion: Although the platform has certain limitations, it nevertheless enables assessment of healthy baseline monocyte, T-, and B-cell responses, and scrutiny of the impact of different stimuli to detect potential immune suppression or enhancement from exogenous materials. In the case of curcumin, a pattern of responses indicative of immune suppressive / anti-inflammatory effects was detected. It is an accessible, highly modifiable system that can be used to screen materials and guide further studies, providing a holistic, integrated picture of effects.