Zhang Hanhao, Bhakta Divya, Saha Anushka, Peddireddy Sai Preetham, Bao Shumin, Li Lei, Handali Sukwan, Secor W Evan, Fraga Lucia A O, Fairley Jessica K, Sarkar Aniruddh
Department of Biomedical Engineering, Georgia Institute of Technology, 315 Ferst Dr NW, Atlanta, GA 30332, USA.
Department of Chemistry and Center for Diagnostics & Therapeutics, Georgia State University, Atlanta, GA, 30303, USA.
Lab Chip. 2025 May 8. doi: 10.1039/d5lc00042d.
Control of endemic infectious diseases is often impeded by the lack of sensitive and specific yet easy-to-obtain biomarkers. Antibody fragment crystallizable (Fc) regions, such as Fc glycosylation, which are modulated in a pathogen-specific and disease-state-specific manner have emerged as potential such biomarkers. However current methods to perform large-scale antigen-specific antibody Fc feature screening for biomarker discovery often require too much sample volume, cost and expertise to be realistically realizable in many disease contexts. Here we present a simple, flexible and reconfigurable microfluidic device, made using rapid prototyping techniques, that can perform highly multiplexed and high-throughput biomarker discovery targeting both antibody fragment antigen-binding (Fab) and Fc features including antigen specificity, antibody isotypes, subclasses, -glycosylation and Fc receptor binding. Using integration of an antigen microarray and reconfigurable microfluidics for sample and probe distribution, the device can perform a total of 1400 assays measuring 100 antibody Fab and Fc features per sample from a low sample volume (15 μL). The device demonstrates cleanroom-free simple fabrication and ease of use comparable to standard immunoassay platforms. Performance comparable to existing methods was validated and a biomarker screening for schistosomiasis, a helminth-mediated infection, was performed using clinical samples where antibody subclass-based biomarkers were successfully identified distinguishing current infection from former infection and endemic controls.
地方性传染病的控制常常因缺乏灵敏、特异且易于获取的生物标志物而受到阻碍。抗体可结晶片段(Fc)区域,如以病原体特异性和疾病状态特异性方式调节的Fc糖基化,已成为潜在的此类生物标志物。然而,目前用于大规模筛选抗原特异性抗体Fc特征以发现生物标志物的方法,在许多疾病情况下,往往需要过多的样本量、成本和专业知识,难以实际实现。在此,我们展示了一种使用快速成型技术制作的简单、灵活且可重新配置的微流控装置,它能够针对抗体片段抗原结合(Fab)和Fc特征(包括抗原特异性、抗体同种型、亚类、糖基化和Fc受体结合)进行高度多重和高通量的生物标志物发现。通过整合抗原微阵列和用于样本及探针分配的可重新配置微流控技术,该装置能够从低样本量(15微升)中对每个样本进行总共1400次测定,测量100种抗体Fab和Fc特征。该装置展示了无需洁净室的简单制造过程,并且与标准免疫测定平台相比易于使用。验证了其与现有方法相当的性能,并使用临床样本对血吸虫病(一种由蠕虫介导的感染)进行了生物标志物筛选,成功鉴定出基于抗体亚类的生物标志物,可区分当前感染与既往感染以及地方性对照。