IgE plasma cells are transcriptionally and functionally distinct from other isotypes

Understanding the phenotypic and transcriptional signature of immunoglobulin E (IgE)-producing cells is fundamental to plasma cell (PC) biology and development of therapeutic interventions for allergy. Here, using a mouse model of intranasal house dust mite (HDM) exposure, we showed that short-lived IgE PCs emerge in lung draining lymph nodes (dLNs) during early exposure (<3 weeks) and long-lived IgE PCs accumulate in the bone marrow (BM) with prolonged exposure (>7 weeks). IgE PCs had distinct surface and gene expression profiles in these different tissues compared with other Ig isotypes. IgE BMPCs up-regulated genes associated with prosurvival and BM homing, whereas IgE dLN PCs expressed genes associated with recent class switching and differentiation. IgE PCs also exhibited higher expression of endoplasmic reticulum (ER) stress and protein coding genes and higher antibody secretion rate when compared with IgG1. Overall, this study highlights the unique developmental path and transcriptional signature of short-lived and long-lived IgE PCs.

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Publication Details

Journal
Science Immunology
Published
2024-09-06
DOI
https://doi.org/10.1126/sciimmunol.adm8964
Citations
23
Primary Topic
Mast cells and histamine
Type
article
Field-Weighted Citation Impact
5.53
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IgE plasma cells are transcriptionally and functionally distinct from other isotypes

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article

IgE plasma cells are transcriptionally and functionally distinct from other isotypes

Seblewongel Asrat, Jamie Marie Orengo, André Limnander, Pierre Bruhns, D Srivastava, Paul Haase, Joseph C. Devlin, Carley Tasker, Gurinder S. Atwal, Matthew A. Sleeman, Venkat Raman Ramnarayan, E. Condé, Wei Keat Lim, Andrew Murphy, Andrea Vecchione
article en
23 citations

Abstract

Understanding the phenotypic and transcriptional signature of immunoglobulin E (IgE)-producing cells is fundamental to plasma cell (PC) biology and development of therapeutic interventions for allergy. Here, using a mouse model of intranasal house dust mite (HDM) exposure, we showed that short-lived IgE PCs emerge in lung draining lymph nodes (dLNs) during early exposure (<3 weeks) and long-lived IgE PCs accumulate in the bone marrow (BM) with prolonged exposure (>7 weeks). IgE PCs had distinct surface and gene expression profiles in these different tissues compared with other Ig isotypes. IgE BMPCs up-regulated genes associated with prosurvival and BM homing, whereas IgE dLN PCs expressed genes associated with recent class switching and differentiation. IgE PCs also exhibited higher expression of endoplasmic reticulum (ER) stress and protein coding genes and higher antibody secretion rate when compared with IgG1. Overall, this study highlights the unique developmental path and transcriptional signature of short-lived and long-lived IgE PCs.

Science ImmunologyVol. 9(99)
Inserm (FR), Institut Pasteur (FR), Regeneron (United States) (US), Université Paris Cité (FR)
Good health and well-being
Openalex Percentile: Top 3%
Mast cells and histamine
5.53
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