{"title":"使用无血清培养基进行外周血单核细胞培养及其对 T 细胞和 B 细胞读数的影响。","authors":"Stella Cochrane, Ouarda Saib, David Sheffield","doi":"10.3389/ftox.2024.1462688","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>As part of a wider programme of work developing next-generation risk assessment approaches (NGRA) using non-animal methods (NAMs) for safety assessment of materials, Unilever SEAC is exploring the use of a peripheral blood mononuclear cell (PBMC) system to investigate how cells from different arms of the human immune system are impacted by different treatments. To maximise human relevance, the cell cultures are supported by human serum, but this came with some challenges, including an inability to measure induced levels of immunoglobulins due to high background levels. Therefore, a study comparing use of human sera containing media with three different chemically defined serum-free media was undertaken.</p><p><strong>Materials and methods: </strong>PBMC were isolated from healthy donors and cultured in the absence (media alone) or presence of stimulation reagents (CpG-ODN plus IL-15, Pokeweed Mitogen (PWM) or Cytostim (CS)), in RPMI plus human serum, AIM-V, CTS OpTmizer T cell expansion SFM or X-VIVO 15 media. T cell (CD4<sup>+</sup> and CD8<sup>+</sup>) and B cell proliferation and viability were measured after 6 days, along with levels of total IgG in the cell culture supernatants.</p><p><strong>Results: </strong>Each of the serum-free media tested supported good levels of viable and proliferating T cells and B cells over the 6 days of culture, with only a few, small differences across the media, when there was no stimulation. They also enabled detection of a stimulation-evoked increase in IgG levels. There were however some differences in the viability and proliferation responses of T and B cells, to different stimuli, across the different media.</p><p><strong>Discussion: </strong>The serum-free media formulations tested in this study offer defined systems for. measuring B cell IgG responses, <i>in vitro</i>, in either a 'T cell-independent' (CpG + IL-15) or \"T cell-dependent\" (PWM or CS) manner and for assessing B cell proliferation, particularly in response to a \"T cell-independent\" stimulus. However, there are some characteristics and features endowed by human serum that appear to be missing. Therefore, further work is required to optimise animal-free, chemically defined culture conditions for PBMC based assays for inclusion in tiered safety assessments.</p>","PeriodicalId":73111,"journal":{"name":"Frontiers in toxicology","volume":"6 ","pages":"1462688"},"PeriodicalIF":3.6000,"publicationDate":"2024-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11573784/pdf/","citationCount":"0","resultStr":"{\"title\":\"Use of serum-free media for peripheral blood mononuclear cell culture and the impact on T and B cell readouts.\",\"authors\":\"Stella Cochrane, Ouarda Saib, David Sheffield\",\"doi\":\"10.3389/ftox.2024.1462688\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>As part of a wider programme of work developing next-generation risk assessment approaches (NGRA) using non-animal methods (NAMs) for safety assessment of materials, Unilever SEAC is exploring the use of a peripheral blood mononuclear cell (PBMC) system to investigate how cells from different arms of the human immune system are impacted by different treatments. To maximise human relevance, the cell cultures are supported by human serum, but this came with some challenges, including an inability to measure induced levels of immunoglobulins due to high background levels. Therefore, a study comparing use of human sera containing media with three different chemically defined serum-free media was undertaken.</p><p><strong>Materials and methods: </strong>PBMC were isolated from healthy donors and cultured in the absence (media alone) or presence of stimulation reagents (CpG-ODN plus IL-15, Pokeweed Mitogen (PWM) or Cytostim (CS)), in RPMI plus human serum, AIM-V, CTS OpTmizer T cell expansion SFM or X-VIVO 15 media. T cell (CD4<sup>+</sup> and CD8<sup>+</sup>) and B cell proliferation and viability were measured after 6 days, along with levels of total IgG in the cell culture supernatants.</p><p><strong>Results: </strong>Each of the serum-free media tested supported good levels of viable and proliferating T cells and B cells over the 6 days of culture, with only a few, small differences across the media, when there was no stimulation. They also enabled detection of a stimulation-evoked increase in IgG levels. There were however some differences in the viability and proliferation responses of T and B cells, to different stimuli, across the different media.</p><p><strong>Discussion: </strong>The serum-free media formulations tested in this study offer defined systems for. measuring B cell IgG responses, <i>in vitro</i>, in either a 'T cell-independent' (CpG + IL-15) or \\\"T cell-dependent\\\" (PWM or CS) manner and for assessing B cell proliferation, particularly in response to a \\\"T cell-independent\\\" stimulus. However, there are some characteristics and features endowed by human serum that appear to be missing. Therefore, further work is required to optimise animal-free, chemically defined culture conditions for PBMC based assays for inclusion in tiered safety assessments.</p>\",\"PeriodicalId\":73111,\"journal\":{\"name\":\"Frontiers in toxicology\",\"volume\":\"6 \",\"pages\":\"1462688\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2024-11-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11573784/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Frontiers in toxicology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3389/ftox.2024.1462688\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"TOXICOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in toxicology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3389/ftox.2024.1462688","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"TOXICOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
简介:联合利华 SEAC 正在探索使用外周血单核细胞 (PBMC) 系统来研究人体免疫系统不同臂膀的细胞如何受到不同治疗方法的影响,这是开发使用非动物方法 (NAM) 进行材料安全评估的下一代风险评估方法 (NGRA) 的广泛工作计划的一部分。为了最大限度地贴近人体,细胞培养使用了人血清,但这也带来了一些挑战,包括由于本底水平较高而无法测量诱导的免疫球蛋白水平。因此,我们进行了一项研究,比较使用含人血清培养基和三种不同化学定义的无血清培养基:从健康捐献者身上分离出 PBMC,在无刺激试剂(单独培养基)或有刺激试剂(CpG-ODN 加 IL-15、Pokeweed Mitogen (PWM) 或 Cytostim (CS))的情况下,在 RPMI 加人血清、AIM-V、CTS OpTmizer T 细胞扩增 SFM 或 X-VIVO 15 培养基中进行培养。6 天后测量 T 细胞(CD4+ 和 CD8+)和 B 细胞的增殖和活力,以及细胞培养上清中总 IgG 的水平:结果:所测试的每种无血清培养基都能在 6 天的培养过程中支持较高水平的存活和增殖 T 细胞和 B 细胞,在没有刺激的情况下,不同培养基之间的差异很小。它们还能检测到刺激引起的 IgG 水平的增加。不过,不同培养基中的 T 细胞和 B 细胞对不同刺激的活力和增殖反应存在一些差异:本研究中测试的无血清培养基配方为体外测量 B 细胞 IgG 反应提供了明确的系统,这些反应可以是 "T 细胞依赖型"(CpG + IL-15)或 "T 细胞依赖型"(PWM 或 CS),也可用于评估 B 细胞增殖,特别是对 "T 细胞依赖型 "刺激的反应。然而,人类血清所具有的一些特性和特征似乎还存在缺失。因此,需要进一步开展工作,优化基于 PBMC 分析的无动物、化学定义的培养条件,以便纳入分级安全评估。
Use of serum-free media for peripheral blood mononuclear cell culture and the impact on T and B cell readouts.
Introduction: As part of a wider programme of work developing next-generation risk assessment approaches (NGRA) using non-animal methods (NAMs) for safety assessment of materials, Unilever SEAC is exploring the use of a peripheral blood mononuclear cell (PBMC) system to investigate how cells from different arms of the human immune system are impacted by different treatments. To maximise human relevance, the cell cultures are supported by human serum, but this came with some challenges, including an inability to measure induced levels of immunoglobulins due to high background levels. Therefore, a study comparing use of human sera containing media with three different chemically defined serum-free media was undertaken.
Materials and methods: PBMC were isolated from healthy donors and cultured in the absence (media alone) or presence of stimulation reagents (CpG-ODN plus IL-15, Pokeweed Mitogen (PWM) or Cytostim (CS)), in RPMI plus human serum, AIM-V, CTS OpTmizer T cell expansion SFM or X-VIVO 15 media. T cell (CD4+ and CD8+) and B cell proliferation and viability were measured after 6 days, along with levels of total IgG in the cell culture supernatants.
Results: Each of the serum-free media tested supported good levels of viable and proliferating T cells and B cells over the 6 days of culture, with only a few, small differences across the media, when there was no stimulation. They also enabled detection of a stimulation-evoked increase in IgG levels. There were however some differences in the viability and proliferation responses of T and B cells, to different stimuli, across the different media.
Discussion: The serum-free media formulations tested in this study offer defined systems for. measuring B cell IgG responses, in vitro, in either a 'T cell-independent' (CpG + IL-15) or "T cell-dependent" (PWM or CS) manner and for assessing B cell proliferation, particularly in response to a "T cell-independent" stimulus. However, there are some characteristics and features endowed by human serum that appear to be missing. Therefore, further work is required to optimise animal-free, chemically defined culture conditions for PBMC based assays for inclusion in tiered safety assessments.