Plasma cells are not restricted to the CD27+ phenotype: characterization of CD27-CD43+ antibody-secreting cells

Kris Covens, Bert Verbinnen, Britt G. de Jong, Leen Moens, Greet Wuyts, Geert Verheyen, Kris Nys, Jonathan Cremer, Stijn Smulders, Rik Schrijvers, Andreas Weinhäusel, Séverine Vermeire, Patrick Verschueren, Ellen De Langhe, Jacques J.M. van Dongen, Menno C. van Zelm, Xavier Bossuyt*

*Corresponding author for this work

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

Circulating antibody-secreting cells are present in the peripheral blood of healthy individuals reflecting the continued activity of the humoral immune system. Antibody-secreting cells typically express CD27. Here we describe and characterize a small population of antibody-secreting class switched CD19+CD43+ B cells that lack expression of CD27 in the peripheral blood of healthy subjects. In this study, we characterized CD27-CD43+ cells. We demonstrate that class-switched CD27-CD43+ B cells possess characteristics of conventional plasmablasts as they spontaneously secrete antibodies, are morphologically similar to antibody-secreting cells, show downregulation of B cell differentiation markers, and have a gene expression profile related to conventional plasmablasts. Despite these similarities, we observed differences in IgA and IgG subclass distribution, expression of homing markers, replication history, frequency of somatic hypermutation, immunoglobulin repertoire, gene expression related to Toll-like receptors, cytokines, and cytokine receptors, and antibody response to vaccination. Their frequency is altered in immune-mediated disorders. Conclusion: we characterized CD27-CD43+ cells as antibody-secreting cells with differences in function and homing potential as compared to conventional CD27+ antibody-secreting cells.

Original languageEnglish
Article number1165936
Pages (from-to)1-16
Number of pages16
JournalFrontiers in Immunology
Volume14
DOIs
Publication statusPublished - 10 Jul 2023

Bibliographical note

Funding Information:
This study was supported by a research grant from the Research Council of the KU Leuven (GOA/13/013). KC and BV were supported through a grant from the Flemish Institute for Innovation through Science and Technology. Acknowledgments

Publisher Copyright:
Copyright © 2023 Covens, Verbinnen, de Jong, Moens, Wuyts, Verheyen, Nys, Cremer, Smulders, Schrijvers, Weinhäusel, Vermeire, Verschueren, Langhe, van Dongen, van Zelm and Bossuyt.

Funding

This study was supported by a research grant from the Research Council of the KU Leuven (GOA/13/013). KC and BV were supported through a grant from the Flemish Institute for Innovation through Science and Technology. Acknowledgments

FundersFunder number
Flemish Institute for Innovation
KU LeuvenGOA/13/013
KU Leuven

    Keywords

    • antibody secreting cells
    • B lymphocyte
    • CD27
    • CD43
    • plasmablast
    • somatic hypermutation

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