Maturation of human early-minted blood antibody-secreting cells is coupled with increased IgG secretion rates

Plasma cells are known antibody-secreting factories with immunoglobulin (Ig) transcripts that increase as the cell matures into a long-lived plasma cell (LLPC) in the bone marrow (BM). Whether the Ig secretion rates among human antibody-secreting cells (ASC) are homogeneous or BM LLPC are capable of secreting more antibodies per cell compared to early-minted blood ASC remain unclear. Here, we use bulk and single cell cultures in a novel <i>in vitro</i> BM mimetic survival system to measure the IgG secretion rates of human ASC. We find that the mature BM ASC produce more IgG molecules per cell compared to immature, early-minted blood ASC. Furthermore, these blood ASC can mature into LLPC phenotypes in culture, and we show that ASC on day 7 secrete more IgG per cell than the input ASC from day 0. Thus, as human ASC mature, they increase the number of Ig transcripts and result in higher Ig secretion. These results also demonstrate that the mature ASC in the BM have higher Ig secretion rates compared to early-minted blood ASC.

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Publication Details

Journal
Frontiers in Immunology
Published
2025-09-02
DOI
https://doi.org/10.3389/fimmu.2025.1644102
Citations
2
Primary Topic
Glycosylation and Glycoproteins Research
Type
article
Field-Weighted Citation Impact
1.61

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article

Maturation of human early-minted blood antibody-secreting cells is coupled with increased IgG secretion rates

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2 citations
Frontiers in Immunology
Glycosylation and Glycoproteins Research
1.61
article

Maturation of human early-minted blood antibody-secreting cells is coupled with increased IgG secretion rates

Doan C. Nguyen, F. Eun‐Hyung Lee, Sagar Lonial, Joel Andrews, Natalie S. Haddad, Shuya Kyu, Danielle Roberts, Monica Cabrera-Mora, Igñacio Sanz, Ian Hentenaar, Andrea Morrison-Porter
article en
2 citations

Abstract

Plasma cells are known antibody-secreting factories with immunoglobulin (Ig) transcripts that increase as the cell matures into a long-lived plasma cell (LLPC) in the bone marrow (BM). Whether the Ig secretion rates among human antibody-secreting cells (ASC) are homogeneous or BM LLPC are capable of secreting more antibodies per cell compared to early-minted blood ASC remain unclear. Here, we use bulk and single cell cultures in a novel <i>in vitro</i> BM mimetic survival system to measure the IgG secretion rates of human ASC. We find that the mature BM ASC produce more IgG molecules per cell compared to immature, early-minted blood ASC. Furthermore, these blood ASC can mature into LLPC phenotypes in culture, and we show that ASC on day 7 secrete more IgG per cell than the input ASC from day 0. Thus, as human ASC mature, they increase the number of Ig transcripts and result in higher Ig secretion. These results also demonstrate that the mature ASC in the BM have higher Ig secretion rates compared to early-minted blood ASC.

Frontiers in ImmunologyVol. 16
Emory University (US)
Bill and Melinda Gates Foundation, Emory University, National Institutes of Health, National Institute of Allergy and Infectious Diseases
Openalex Percentile: Top 15%
Glycosylation and Glycoproteins Research
1.61
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