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B cell CD19 is transferred between immune cells in mice and humans

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Item Type:Article
Title:B cell CD19 is transferred between immune cells in mice and humans
Creators: Ochs, Jasmin, Schweineberg, Pia, Thode, Jacqueline, Blenkle, Alica ORCID logoORCID: https://orcid.org/0000-0002-4641-1863, Husseini, Leila, Klein, Matthias, Bopp, Tobias ORCID logoORCID: https://orcid.org/0000-0002-3232-8065, Schindler, Patrick, Paul, Friedemann ORCID logoORCID: https://orcid.org/0000-0002-6378-0070 and Weber, Martin S. ORCID logoORCID: https://orcid.org/0000-0001-8409-0389
Abstract:When immune cells interact, they frequently exchange membrane-bound antigens. Our evolving understanding of these processes challenges the cellular specificity of lineage markers and therapeutic monoclonal antibodies. By using mouse and human B-T cell co-cultures, we report that CD19, an assumingly exclusive B cell marker, is transferred via trogocytosis when B cells activate T cells. In a B cell-driven model of experimental autoimmune encephalomyelitis, CD19(+) T cells expand and show enhanced features of activation, differentiation, and encephalitogenic potential ex vivo. Additionally, co-transfer of CD19 and functional IgM from B cells results in the gain of B cell function by T cells. In patients with chronic central nervous system (CNS) demyelination, CD19(+) T cells display a pro-inflammatory phenotype and are concomitantly depleted by inebilizumab, an approved anti-CD19 antibody, which raises important considerations for the therapeutic use of monoclonal antibodies overall. Finally, we report that myeloid cells acquire CD19 and functional IgM after phagocytosis of apoptotic B cells and thereby gain functional B cell properties. These findings highlight the commonness of membrane and antigen-transfer between cells, resulting in transmission of cellular function.
Keywords:B-Lymphocytes, CD19 Antigens, Coculture Techniques, Experimental Autoimmune Encephalomyelitis, Immunoglobulin M, Inbred C57BL Mice, Lymphocyte Activation, T-Lymphocytes, Trogocytosis, Animals, Mice
Source:Nature Communications
ISSN:2041-1723
Publisher:Nature Publishing Group
Volume:17
Number:1
Page Range:7588
Date:29 July 2026
Official Publication:https://doi.org/10.1038/s41467-026-75534-3
PubMed:View item in PubMed
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