IL-21 in Conjunction with Anti-CD40 and IL-4 Constitutes a Potent Polyclonal B Cell Stimulator for Monitoring Antigen-Specific Memory B Cells

被引:22
作者
Franke, Fridolin [1 ,2 ]
Kirchenbaum, Greg A. [1 ]
Kuerten, Stefanie [2 ]
Lehmann, Paul V. [1 ]
机构
[1] Cellular Technol Ltd, Res & Dev Dept, Shaker Hts, OH 44122 USA
[2] Friedrich Alexander Univ Erlangen Nurnberg, Inst Anat & Cell Biol, D-91054 Erlangen, Germany
关键词
antibody-secreting cells; B cell activation; plasmablasts; IgE; ELISPOT; ImmunoSpot; Fluorospot; immunoglobulin classes; influenza; type; 1; allergy; PLASMA-CELLS; HUMAN NAIVE; MONOCLONAL-ANTIBODIES; SECRETING CELLS; IGE PRODUCTION; ELISPOT ASSAY; UP-REGULATION; DIFFERENTIATION; PROLIFERATION; LYMPHOCYTES;
D O I
10.3390/cells9020433
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Detection of antigen-specific memory B cells for immune monitoring requires their activation, and is commonly accomplished through stimulation with the TLR7/8 agonist R848 and IL-2. To this end, we evaluated whether addition of IL-21 would further enhance this TLR-driven stimulation approach; which it did not. More importantly, as most antigen-specific B cell responses are T cell-driven, we sought to devise a polyclonal B cell stimulation protocol that closely mimics T cell help. Herein, we report that the combination of agonistic anti-CD40, IL-4 and IL-21 affords polyclonal B cell stimulation that was comparable to R848 and IL-2 for detection of influenza-specific memory B cells. An additional advantage of anti-CD40, IL-4 and IL-21 stimulation is the selective activation of IgM(+) memory B cells, as well as the elicitation of IgE(+) ASC, which the former fails to do. Thereby, we introduce a protocol that mimics physiological B cell activation through helper T cells, including induction of all Ig classes, for immune monitoring of antigen-specific B cell memory.
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页数:16
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