PBMC and fibroblast cocultures to mimic the in vivo effect of BCG on trained immunity.

microPublication biology Pub Date : 2025-02-05 eCollection Date: 2025-01-01 DOI:10.17912/micropub.biology.001449
David Merriam, Adriana Weinberg
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Abstract

BCG greatly stimulates innate immune cells. Previous studies demonstrated that BCG-stimulated monocytes develop trained immunity whereby they respond to homologous and heterologous antigens. Previous studies used isolated monocytes or animal models to study BCG-induced trained immunity, which have benefits and limitations. To approximate in vivo conditions, we stimulated peripheral blood mononuclear cells (PBMCs) with BCG-treated human fibroblasts. We found that compared with BCG stimulation, the addition of fibroblasts increased the expression of IFN-γ in NK and γδ T cells and of TNF-α and IL-10 in monocytes. We conclude that BCG-treated fibroblasts offer advantages over BCG alone for studying trained immunity.

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PBMC与成纤维细胞共培养以模拟卡介苗对训练免疫的体内效应。
卡介苗极大地刺激先天免疫细胞。先前的研究表明,bcg刺激的单核细胞产生训练免疫,从而对同源和异源抗原作出反应。先前的研究使用分离的单核细胞或动物模型来研究bcg诱导的训练免疫,这有其优点和局限性。为了模拟体内条件,我们用bcg处理的人成纤维细胞刺激外周血单个核细胞(PBMCs)。我们发现,与BCG刺激相比,成纤维细胞的加入增加了NK细胞和γδ T细胞中IFN-γ的表达以及单核细胞中TNF-α和IL-10的表达。我们得出结论,BCG处理的成纤维细胞在研究训练免疫方面比单独BCG有优势。
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