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Surface-Micromachined Microfiltration Membranes for Efficient Isolation and Functional Immunophenotyping of Subpopulations of Immune Cells

机译:表面微加工微滤膜的高效分离和免疫细胞亚群的功能免疫分型

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摘要

An accurate measurement of the immune status in patients with immune system disorders is critical in evaluating the stage of diseases and tailoring drug treatments. The functional cellular immunity test is a promising method to establish the diagnosis of immune dysfunctions. The conventional functional cellular immunity test involves measurements of the capacity of peripheral blood mononuclear cells to produce pro-inflammatory cytokines when stimulated ex vivo. However, this “bulk” assay measures the overall reactivity of a population of lymphocytes and monocytes, making it difficult to pinpoint the phenotype or real identity of the reactive immune cells involved. In this research, we develop a large surface micromachined polydimethylsiloxane (PDMS) microfiltration membrane (PMM) with high porosity, which is integrated in a microfluidic microfiltration platform. Using the PMM with functionalized microbeads conjugated with antibodies against specific cell surface proteins, we demonstrated rapid, efficient and high-throughput on-chip isolation, enrichment, and stimulation of subpopulations of immune cells from blood specimens. Furthermore, the PMM-integrated microfiltration platform, coupled with a no-wash homogeneous chemiluminescence assay (“AlphaLISA”), enables us to demonstrate rapid and sensitive on-chip immunophenotyping assays for subpopulations of immune cells isolated directly from minute quantities of blood samples.
机译:免疫系统疾病患者的免疫状态的准确测量对于评估疾病阶段和调整药物治疗至关重要。功能性细胞免疫测试是建立免疫功能障碍诊断的一种有前途的方法。常规功能性细胞免疫测试涉及离体刺激时外周血单核细胞产生促炎性细胞因子的能力的测量。然而,这种“大量”测定法测量了一群淋巴细胞和单核细胞的总体反应性,使得很难查明所涉及的反应性免疫细胞的表型或真实身份。在这项研究中,我们开发了一种具有高孔隙率的大表面微机械加工的聚二甲基硅氧烷(PDMS)微滤膜(PMM),该膜已集成在微流体微滤平台中。通过将PMM与功能化的微珠与针对特定细胞表面蛋白的抗体缀合,我们证明了快速,高效和高通量的芯片上分离,富集和刺激了血液样本中免疫细胞的亚群。此外,与PMM集成的微滤平台与免洗的均匀化学发光测定法(“ AlphaLISA”)相结合,使我们能够展示快速,灵敏的片上免疫表型测定法,用于直接从微量血液样品中分离的免疫细胞亚群。

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