Functional Enrichment and Analysis of Antigen-Specific Memory B Cell Antibody Repertoires in PBMCs

被引:12
|
作者
Waltari, Eric [1 ]
McGeever, Aaron [1 ]
Friedland, Natalia [2 ,3 ]
Kim, Peter S. [1 ,2 ,3 ]
McCutcheon, Krista M. [1 ]
机构
[1] Chan Zuckerberg Biohub, San Francisco, CA 94158 USA
[2] Stanford Univ, Sch Med, Stanford ChEM H, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Biochem, Stanford, CA 94305 USA
来源
FRONTIERS IN IMMUNOLOGY | 2019年 / 10卷
关键词
antibody; repertoire; sequencing; memory B cell; PBMC; clonal families; DYNAMICS; VACCINES; TOOLKIT;
D O I
10.3389/fimmu.2019.01452
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Phenotypic screening of antigen-specific antibodies in human blood is a common diagnostic test for infectious agents and a correlate of protection after vaccination. In addition to long-lived antibody secreting plasma cells residing in the bone marrow, memory B cells are a latent source of antigen-experienced, long-term immunity that can be found at low frequencies in circulating peripheral blood mononuclear cells (PBMCs). Assessing the genotype, clonal frequency, quality, and function of antibodies resulting from an individual's persistent memory B cell repertoire can help inform the success or failure of immune protection. Using in vitro polyclonal stimulation, we functionally expand the memory repertoire from PBMCs and clonally map monoclonal antibodies from this population. We show that combining deep sequencing of stimulated memory B cell repertoires with retrieving single antigen-specific cells is a promising approach in evaluating the latent, functional B cell memory in PBMCs.
引用
收藏
页数:17
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