Functional Characterization of CD11c+ Age-Associated B Cells as Memory B Cells
Samuel W Du1, Tanvi Arkatkar1, Fahd Al Qureshah1,2,3
1Seattle Children's Research Institute, Seattle, WA 98101.
Journal of Immunology (Baltimore, Md. : 1950)
|October 23, 2019
Summary
Age-associated B cells (ABCs) are identified as memory B cells (MBCs) with a history of antigen exposure and potential for rapid antibody production. These cells, expressing IgM, are implicated in systemic autoimmunity.
Area of Science:
- Immunology
- Cell Biology
Background:
- Age-associated B cells (ABCs) are a distinct B cell subset characterized by CD11b and CD11c expression.
- ABCs expand with age, autoimmunity, and viral infections, but their function is not fully understood.
Purpose of the Study:
- To define the functional properties of ABCs.
- To determine if ABCs meet the criteria for memory B cells (MBCs).
Main Methods:
- Analysis of ABC replication history and surface markers.
- Cloning and characterization of B cell receptors (BCRs) from ABCs.
- Assessment of ABC differentiation potential in a viral infection model.
Main Results:
- ABCs show evidence of prior antigen engagement and somatic hypermutation, despite IgM expression.
- ABCs exhibit autoreactivity and polyreactivity without functional anergy.
- ABCs express MBC markers and differentiate into antibody-secreting cells upon rechallenge.
Conclusions:
- ABCs are functionally characterized as IgM-expressing memory B cells (MBCs).
- These findings suggest ABCs contribute to the pathogenesis of systemic autoimmunity.
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