Development of a high-throughput image cytometric screening method as a research tool for immunophenotypic characterization of patient samples from clinical studies

免疫分型 细胞仪 流式细胞术 CD19 CD3型 外周血单个核细胞 分化群 CD14型 免疫学 生物 病理 医学 免疫系统 细胞 CD8型 体外 生物化学 遗传学
作者
Samir N. Patel,James I. McDonald,Hamza Yelwa Mohammed,Vaishnavi Parthasarathy,Veronica Hernandez,Tyanna Stuckey,Allen H. Lin,Srinivas Koushik Gundimeda,Bo Lin,Julian Reading,Leo Li‐Ying Chan
出处
期刊:Journal of Immunological Methods [Elsevier BV]
卷期号:524: 113587-113587
标识
DOI:10.1016/j.jim.2023.113587
摘要

Immunophenotyping has been the primary assay for characterization of immune cells from patients undergoing therapeutic treatments in clinical research, which is critical for understanding disease progression and treatment efficacy. Currently, flow cytometry has been the dominant methodology for characterizing surface marker expression for immunological research. Flow cytometry has been proven to be an effective and efficient method for immunophenotyping, however, it requires highly trained users and a large time commitment. Recently, a novel image cytometry system (Cellaca® PLX Image Cytometer, Revvity Health Sciences, Inc., Lawrence, MA) has been developed as a complementary method to flow cytometry for performing rapid and high-throughput immunophenotyping. In this work, we demonstrate an image cytometric screening method to characterize immune cell populations, streamlining the analysis of routine surface marker panels. The T cell, B cell, NK cell, and monocyte populations of 46 primary PBMC samples from subjects enrolled in autoimmune and oncological disease study cohorts were analyzed with two optimized immunophenotyping staining kits: Panel 1 (CD3, CD56, CD14) and Panel 2 (CD3, CD56, CD19). We validated the proposed image cytometry method by comparing the Cellaca® PLX and the Aurora cytometer (Cytek Biosciences, Fremont, CA). The image cytometry system was employed to generate bright field and fluorescent images, as well as scatter plots for multiple patient PBMC samples. In addition, the image cytometry method can directly determine cell concentrations for downstream assays. The results demonstrated comparable CD3, CD14, CD19, and CD56 cell populations from the primary PBMC samples, which showed an average of 5% differences between flow and image cytometry. The proposed image cytometry method provides a novel research tool to streamline immunophenotyping workflow for characterizing patient samples in clinical studies.
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