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Updated: Jul 5, 2026

In Vitro Differentiation Model of Human Normal Memory B Cells to Long-lived Plasma Cells
Published on: January 20, 2019
Molecular and tissue regulation of memory B cells
Mauro Gaya1, Kim L Good-Jacobson2
1Centre d'Immunologie de Marseille-Luminy (CIML), Aix Marseille Université, INSERM, CNRS, Marseille, France.
None:
Memory B cells underpin the capacity of the immune system to confer durable protective immunity by mounting rapid and enhanced secondary antibody responses. Hence, they are central to vaccine efficacy and to limiting long-term tissue damage after reinfection. Despite their importance, the cellular origins, molecular programs, and tissue-specific specialization of memory B cells remain incompletely understood. Here, we review recent advances in memory B cell development and regulation, with a particular focus on tissue-resident memory B cells. We discuss how memory B cells arise from distinct developmental precursors as well as the extrinsic regulators and molecular programs that govern memory B cell identity and function. We further examine emerging evidence for tissue-resident memory B cell populations in the respiratory airways and their implications for mucosal vaccination strategies against airborne pathogens. Together, these findings provide a framework for leveraging memory B cell biology in clinical applications.
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