Gregory Fleming James Cystic Fibrosis Research Center, University of Alabama at Birmingham, Birmingham, Alabama.
Division of Pulmonary and Sleep Medicine, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama.
Am J Physiol Lung Cell Mol Physiol. 2021 Jul 1;321(1):L119-L129. doi: 10.1152/ajplung.00639.2020. Epub 2021 May 19.
In vitro biomarkers to assess cystic fibrosis transmembrane conductance regulator activity are desirable for precision modulator selection and as a tool for clinical trials. Here, we describe an organoid swelling assay derived from human nasal epithelia using commercially available reagents and equipment and an automated imaging process. Cells were collected in nasal brush biopsies, expanded in vitro, and cultured as spherical organoids or as monolayers. Organoids were used in a functional swelling assay with automated measurements and analysis, whereas monolayers were used for short-circuit current measurements to assess ion channel activity. Clinical data were collected from patients on modulators. Relationships between swelling data and short-circuit current, as well as between swelling data and clinical outcome measures, were assessed. The organoid assay measurements correlated with short-circuit current measurements for ion channel activity. The functional organoid assay distinguished individual responses as well as differences between groups. The organoid assay distinguished incremental drug responses to modulator monotherapy with ivacaftor and combination therapy with ivacaftor, tezacaftor, and elexacaftor. The swelling activity paralleled the clinical response. In conclusion, an in vitro biomarker derived from patients' cells can be used to predict responses to drugs and is likely to be useful as a preclinical tool to aid in the development of novel treatments and as a clinical trial outcome measure for a variety of applications, including gene therapy or editing.
评估囊性纤维化跨膜电导调节剂活性的体外生物标志物是精准调节剂选择的理想工具,也是临床试验的工具。在这里,我们描述了一种源自人鼻上皮的类器官肿胀测定法,该方法使用市售试剂和设备以及自动化成像过程。细胞从鼻刷活检中收集,在体外扩增,并培养为球形类器官或单层。使用自动化测量和分析的功能性肿胀测定法对类器官进行测试,而使用单层进行评估离子通道活性的短路电流测量。从接受调节剂治疗的患者中收集临床数据。评估肿胀数据与短路电流之间的关系,以及肿胀数据与临床结果测量之间的关系。类器官测定的测量结果与离子通道活性的短路电流测量结果相关。功能性类器官测定法区分了个体反应以及组间差异。类器官测定法区分了伊伐卡托单药治疗和伊伐卡托、特扎卡托和埃利卡托联合治疗的增量药物反应。肿胀活性与临床反应平行。总之,源自患者细胞的体外生物标志物可用于预测对药物的反应,并且可能作为一种临床前工具,有助于开发新的治疗方法,并作为各种应用的临床试验结果测量指标,包括基因治疗或编辑。