Monoclonal Antibody Generation Using Single B Cell Screening for Treating Infectious Diseases

被引:2
|
作者
Schardt, John S. [1 ,2 ,3 ]
Sivaneri, Neelan S. [2 ,3 ]
Tessier, Peter M. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Univ Michigan, Dept Pharmaceut Sci, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Biointerfaces Inst, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Program Chem Biol, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
DRUG CONJUGATE; LUNG-CANCER; TRASTUZUMAB EMTANSINE; SACITUZUMAB GOVITECAN; PHASE-II; VEDOTIN; SAFETY; TUMORS;
D O I
10.1007/s40259-024-00667-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The screening of antigen-specific B cells has been pivotal for biotherapeutic development for over four decades. Conventional antibody discovery strategies, including hybridoma technology and single B cell screening, remain widely used based on their simplicity, accessibility, and proven track record. Technological advances and the urgent demand for infectious disease applications have shifted paradigms in single B cell screening, resulting in increased throughput and decreased time and labor, ultimately enabling the rapid identification of monoclonal antibodies with desired biological and biophysical properties. Herein, we provide an overview of conventional and emergent single B cell screening approaches and highlight their potential strengths and weaknesses. We also detail the impact of innovative technologies-including miniaturization, microfluidics, multiplexing, and deep sequencing-on the recent identification of broadly neutralizing antibodies for infectious disease applications. Overall, the coronavirus disease 2019 (COVID-19) pandemic has reinvigorated efforts to improve the efficiency of monoclonal antibody discovery, resulting in the broad application of innovative antibody discovery methodologies for treating a myriad of infectious diseases and pathological conditions.
引用
收藏
页码:477 / 486
页数:10
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