单克隆抗体
细胞
计算生物学
抗体
化学
分子生物学
病毒学
纳米技术
生物
免疫学
材料科学
生物化学
作者
Julie Van Lent,Jolien Breukers,Karen Ven,Louanne Ampofo,Sara Horta,Francesca Pollet,Maya Imbrechts,Nick Geukens,Karen Vanhoorelbeke,Paul Declerck,Jeroen Lammertyn
出处
期刊:Lab on a Chip
[Royal Society of Chemistry]
日期:2021-01-01
卷期号:21 (19): 3627-3654
被引量:21
摘要
Antibodies (Abs) are among the most important class of biologicals, showcasing a high therapeutic and diagnostic value. In the global therapeutic Ab market, fully-human monoclonal Abs (FH-mAbs) are flourishing thanks to their low immunogenicity and high specificity. The rapidly emerging field of single-cell technologies has paved the way to efficiently discover mAbs by facilitating a fast screening of the antigen (Ag)-specificity and functionality of Abs expressed by B cells. This review summarizes the principles and challenges of the four key concepts to discover mAbs using these technologies, being confinement of single cells using either droplet microfluidics or microstructure arrays, identification of the cells of interest, retrieval of those cells and single-cell sequence determination required for mAb production. This review reveals the enormous potential for mix-and-matching of the above-mentioned strategies, which is illustrated by the plethora of established, highly integrated devices. Lastly, an outlook is given on the many opportunities and challenges that still lie ahead to fully exploit miniaturized single-cell technologies for mAb discovery.
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