Multi-step antibody class switching in a primary human response is restricted after IGHG2 and dependent on B cell maturation stage.
Guillem MontamatiD, Joseph Chi-Fung NgiD, Alex StewartiD, Emma L. SinclairiD, Paul A. BlairiD, Diana Kateregga, Amir GanderiD, David KiplingiD, Dongjun GuoiD, Lutecia ServiusiD, Christopher J. M. PiperiD, Zara BaigiD, Franca FraternaliiD, Claudia MauriiD, Deborah K. Dunn‐WaltersiD
Abstract
Class switch recombination (CSR) allows the formation of functionally specialized antibodies. Understanding of CSR dynamics is key for better design and prediction of vaccines to protect mucosal surfaces. To investigate CSR in a primary human immune response under a controlled setting, we sampled healthy volunteers without COVID-19 history every other day during the first three weeks after SARS-CoV-2 vaccination, with additional time points up to six months. Leveraging bulk and single-cell B cell receptor repertoires, single-cell transcriptomics, and immunophenotyping, we uncover paradigm-shifting insights into CSR. Newly activated B cells produce sterile transcripts of all antibody isotype constant regions (IGHC) simultaneously up to IGHG2, challenging the view that sterile transcription occurs for only a single IGHC gene at a time. CSR follows a multistep progression along the IGHC locus; in this challenge vaccine-induced B cells switch from IGHM to IGHG3 and IGHG1, followed by a subsequent switching to IGHA1 and IGHG2 after secondary immunization. IGHA2 clones require pre-switching to IGHA1 clones. Notably, switching tendency, measured by IGHC sterile transcription, is memory B cell subtype dependent, particularly beyond IGHG2. Contrary to other vaccines, antigen-specific B cells are enriched in DN2, Cmem2 and DN4 subtypes after immunization. We also observe a temporal decoupling of CSR and somatic hypermutation (SHM), with the latter detectable only after six months post-immunization. Our data describes the dynamics between CSR, SHM, sterile transcription and B cell memory development during a human primary response, challenges textbook models of CSR and offers new insights to aid control of CSR direction. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=188 HEIGHT=200 SRC="FIGDIR/small/652638v1_ufig1.gif" ALT="Figure 1"> View larger version (49K): org.highwire.dtl.DTLVardef@785769org.highwire.dtl.DTLVardef@b2c54eorg.highwire.dtl.DTLVardef@b78c72org.highwire.dtl.DTLVardef@65b5aa_HPS_FORMAT_FIGEXP M_FIG C_FIG One Sentence SummaryClass switch recombination occurs independently of somatic hypermutation and in a multistep fashion up to IGHG2 during a primary response in humans.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 0
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Human B cell clonal expansion and convergent antibody responses to SARS-CoV-2
Sandra C. A. Nielsen, Fan Yang, … Scott D. Boyd·Cell Host & MicrobePeer-reviewed·Oct 1, 2020
- A dynamic activation-memory cycle organizes the human IgG⁺ memory B cell compartment
Laura T. M. Graus, Andreas Chrysostomou, … Mathieu A. F. Claireaux·bioRxiv·Oct 30, 2025
- Deep profiling of antigen-specific B cells from different pathogens identifies novel compartments in the IgG memory B cell and antibody-secreting cell lineages
M. Claireaux, G. Elias, … S. M. van Ham·bioRxiv·Dec 19, 2023
- B cell maturation restored ancestral germlines to control Omicron BA.2.86
Ida Paciello, Giulio Pierleoni, … Emanuele Andreano·Cell ReportsPeer-reviewed·Aug 27, 2024
- Germinal centre-driven maturation of B cell response to SARS-CoV-2 vaccination
W. Kim, J. Q. Zhou, … A. H. Ellebedy·bioRxiv·Oct 31, 2021
- Rapid hypermutation B cell trajectory recruits previously primed B cells upon third SARS-CoV-2 mRNA vaccination
L. Paschold, B. Klee, … M. Binder·bioRxiv·Mar 1, 2022