Guthmiller Jenna J, Dugan Haley L, Neu Karlynn E, Lan Linda Yu-Ling, Wilson Patrick C
Department of Medicine, Section of Rheumatology, The Knapp Center for Lupus and Immunology, University of Chicago, Chicago, IL, USA.
Committee on Immunology, University of Chicago, Chicago, IL, USA.
Methods Mol Biol. 2019;1904:109-145. doi: 10.1007/978-1-4939-8958-4_5.
In the age of personalized medicine, an efficient method to generate monoclonal antibodies (mAbs) is essential for biomedical and immunotherapeutic research. Numerous aspects of basic B-cell biology can be studied at the monoclonal level, including B-cell development, antibody responses to infection or vaccination, and autoimmune responses. Single-cell B-cell receptor cloning allows for the rapid generation of antigen-specific mAbs in a matter of several weeks. In this chapter, we provide an efficient method to generate mAbs from peripheral blood plasmablasts and memory B cells induced by infection and vaccination. Additionally, we provide a protocol on how to optimize single-cell B-cell sorting for both single-cell B-cell receptor cloning and single-cell RNA-sequencing, for the application of studying B-cell specificity and function (spec-seq). This protocol can be easily adapted for other B-cell populations, B cells in tissues, and B cells from other organisms.
在个性化医疗时代,一种高效生成单克隆抗体(mAb)的方法对于生物医学和免疫治疗研究至关重要。基础B细胞生物学的诸多方面都可在单克隆水平进行研究,包括B细胞发育、对感染或疫苗接种的抗体反应以及自身免疫反应。单细胞B细胞受体克隆能够在短短几周内快速生成抗原特异性单克隆抗体。在本章中,我们提供了一种从感染和疫苗接种诱导的外周血浆母细胞和记忆B细胞中生成单克隆抗体的高效方法。此外,我们还提供了一份关于如何优化单细胞B细胞分选以用于单细胞B细胞受体克隆和单细胞RNA测序的方案,用于研究B细胞特异性和功能(spec-seq)。该方案可轻松适用于其他B细胞群体、组织中的B细胞以及来自其他生物体的B细胞。