Frequency-potency analysis of IgG+ memory B cells delineates neutralizing antibody responses at single-cell resolution

Michelle K. Tenggara, Seo-Ho Oh, Catherine Yang, Hardik K. Nariya, Amanda M. Metz,Amit A. Upadhyay, Dedeepya R. Gudipati, Lizheng Guo, Emily G. McGhee, Kiran Gill,Elise G. Viox, Rosemarie D. Mason,Nicole A. Doria-Rose, Kathryn E. Foulds,John R. Mascola, Yuhong Du,Haian Fu, John D. Altman, Qi Yan,Zizhang Sheng

Cell Reports(2024)

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摘要
Identifying individual functional B cell receptors (BCRs) is common, but two-dimensional analysis of B cell frequency versus BCR potency would delineate both quantity and quality of antigen-specific memory B cells. We efficiently determine quantitative BCR neutralizing activities using a single-cell-derived antibody supernatant analysis (SCAN) workflow and develop a frequency-potency algorithm to estimate B cell frequencies at various neutralizing activity or binding affinity cutoffs. In an HIV-1 fusion peptide (FP) immunization study, frequency-potency curves elucidate the quantity and quality of FP-specific immunoglobulin G (IgG)+ memory B cells for different animals, time points, and antibody lineages at single-cell resolution. The BCR neutralizing activities are mainly determined by their affinities to soluble envelope trimer. Frequency analysis definitively demonstrates dominant neutralizing antibody lineages. These findings establish SCAN and frequency-potency analyses as promising approaches for general B cell analysis and monoclonal antibody (mAb) discovery. They also provide specific rationales for HIV-1 FP-directed vaccine optimization.
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关键词
single-cell-derived antibody supernatant analysis,SCAN,B cell receptor,BCR,frequency,potency,vaccine,antibody,HIV-1,fusion peptide
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