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基于共焦背向散射的流动血样中白血病细胞的检测。

Confocal backscattering-based detection of leukemic cells in flowing blood samples.

机构信息

Biomedical Engineering Department, Tufts University, Medford, Massachusetts 02155, USA.

出版信息

Cytometry A. 2011 Oct;79(10):874-83. doi: 10.1002/cyto.a.21086. Epub 2011 Jun 2.

Abstract

The prognostic value of assessing minimal residual disease (MRD) in leukemia has been established with advancements in flow cytometry and PCR. Nonetheless, these techniques are limited by high equipment costs, complex, and costly cell processing and the need for highly trained personnel. Here, we demonstrate the potential of exploiting differences in the relative intensities of backscattered light at three wavelengths to detect the presence of leukemic cells in samples containing varying mixtures of white blood cells (WBCs) and leukemic cells flowing through microfluidic channels. Using 405, 488, and 633 nm illumination, we identify distinct light scattering intensity distributions for Nalm-6 leukemic cells, normal mononuclear (PBMC) and polymorphonuclear (PMN) white blood cells and red blood cells. We exploit these differences to develop cell classification algorithms, whose performance is evaluated based on simultaneous acquisition of light scattering and fluorescence flow cytometry data. When this algorithm is used prospectively for the analysis of samples consisting of mixtures of PBMCs and leukemic cells, we achieve an average specificity and sensitivity of leukemic cell detection of 99.6 and 45.2%, respectively. When we consider samples that include leukemic cells along with PMNs and PBMCs, which can be acquired using a simple red blood cell lysis step following venipuncture, the specificity and sensitivity of the approach decreases to 91.6 and 39.5%, respectively. On the basis of the performance of these algorithms, we estimate that 42 or 71 μL of blood would be adequate to confirm the presence of leukemia at an 80% power level in samples containing 0.01% leukemia to either PBMCs or PBMCs and PMNs, respectively. Therefore, light scattering-based flow cytometry in a microfluidic platform could provide a low cost, highly portable, minimally invasive approach for detection and monitoring of leukemic patients. This could offer significant improvements especially for pediatric patients and for patients in developing countries.

摘要

利用流式细胞术和聚合酶链反应(PCR)评估微小残留病(MRD)的预后价值已得到确立。然而,这些技术受到设备成本高、细胞处理复杂且昂贵以及对高度训练有素的人员的需求的限制。在这里,我们展示了利用在三个波长的反向散射光的相对强度的差异来检测通过微流控通道流动的含有不同白细胞(WBC)和白血病细胞混合物的样品中白血病细胞存在的潜力。使用 405、488 和 633nm 照明,我们确定了 Nalm-6 白血病细胞、正常单核(PBMC)和多形核(PMN)白细胞和红细胞的独特光散射强度分布。我们利用这些差异开发细胞分类算法,其性能基于同时获取光散射和荧光流式细胞术数据进行评估。当该算法用于前瞻性分析由 PBMC 和白血病细胞混合物组成的样品时,我们实现了白血病细胞检测的平均特异性和敏感性分别为 99.6%和 45.2%。当我们考虑包括PMN 和 PBMC 的白血病细胞以及可以在静脉穿刺后通过简单的红细胞裂解步骤获得的白血病细胞的样品时,该方法的特异性和敏感性分别降低到 91.6%和 39.5%。基于这些算法的性能,我们估计在含有 0.01%白血病的 PBMC 或 PBMC 和 PMN 的样品中,42 或 71μL 的血液足以在 80%的功率水平下确认白血病的存在。因此,基于微流控平台的光散射流式细胞术可以为白血病患者的检测和监测提供一种低成本、高度便携、微创的方法。这将为儿科患者和发展中国家的患者带来重大改善。

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