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Updated: Jun 30, 2026

Murine Model of CD40-activation of B cells
Published on: March 5, 2010
Soluble CD38 significantly prolongs the lifespan of memory B-cell responses
Xue Q Liu1, Derek N J Hart, Gordon G MacPherson
1Queensland Institute of Medical Research, The Bancroft Centre, Brisbane, Qld, Australia.
Insights
Soluble CD38 expands germinal center structures, significantly increasing memory B cell (MBC) numbers and extending their activation period. This enhances antibody memory longevity.
Area of Science:
- Immunology
- Cell Biology
Background:
- Memory B cell (MBC) maintenance relies on germinal centers (GC) and follicular dendritic cell (FDC) networks.
- Previous work identified a novel CD38 ligand on splenic FDC networks, with soluble CD38 administration expanding these structures.
Purpose of the Study:
- To investigate if soluble CD38-induced expansion of FDC networks impacts antigen-specific MBC generation and maintenance.
- To determine the effect of soluble CD38 on the lifespan and frequency of MBC.
Main Methods:
- Adoptive transfer studies were utilized to assess the impact of soluble CD38.
- Analysis focused on the generation, maintenance, and activation potential of antigen-specific MBC following treatment.
Main Results:
- Administration of soluble CD38 significantly extended the duration for MBC activation.
- The frequency of antigen-specific MBC was observably increased after soluble CD38 treatment.
Conclusions:
- Soluble CD38 administration enhances antibody memory by increasing MBC numbers.
- This suggests a therapeutic potential for soluble CD38 in prolonging the lifespan of antibody memory.
Abstract:
The development and maintenance of memory B cells (MBC) is dependent on germinal centres (GC) with follicular dendritic cell (FDC) networks. We have previously shown that FDC networks within GC of the spleen express a novel ligand for CD38 and that the administration of soluble CD38 induces an expansion of these cellular structures. We therefore used adoptive transfer studies to investigate whether the expansion of FDC networks with soluble CD38 affected the generation and maintenance of antigen-specific MBC. These studies found that the administration of soluble CD38 significantly extended the period after which MBC could be activated and that the frequencies of these cells also were increased. In conclusion, soluble CD38 appears to significantly extend the lifespan of antibody memory by increasing the numbers of MBC.
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