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Integrin CD11b provides a new marker of pre-germinal center IgA(+) B cells in murine Peyer’s patches

Activated B cells can enter germinal centers (GCs) for affinity maturation to produce high-affinity antibodies. However, which activated B cells will enter GCs remains unknown. Here, we found a small population of CD11b(+)IgA(+) B cells located outside of GCs in murine Peyer’s patches (PPs). After i...

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Detalles Bibliográficos
Autores principales: Gao, Peng, Adachi, Takahiro, Okai, Shinsaku, Morita, Naoki, Kitamura, Daisuke, Shinkura, Reiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9020567/
https://www.ncbi.nlm.nih.gov/pubmed/34971392
http://dx.doi.org/10.1093/intimm/dxab113
Descripción
Sumario:Activated B cells can enter germinal centers (GCs) for affinity maturation to produce high-affinity antibodies. However, which activated B cells will enter GCs remains unknown. Here, we found a small population of CD11b(+)IgA(+) B cells located outside of GCs in murine Peyer’s patches (PPs). After injection of the CD11b(+)IgA(+) PP B cells into a PP of a recipient mouse, they entered GCs forty hours later. They expressed GC surface markers and pre-GC B cell genes, suggesting that CD11b provides a novel surface marker of pre-GC IgA(+) B cells in murine PPs. Furthermore, independently of dendritic cell activation, CD11b expression on B cells can be induced by bacterial antigens, such as pam3CSK4 and heat-killed Escherichia coli in vitro. In addition, mice orally administered with pam3CSK4 or heat-killed E. coli increased the number of PP GC B cells within two days, and enhanced the mucosal antigen-specific IgA response. Our results demonstrate that the induction of CD11b on B cells is a promising marker for selecting an effective mucosal vaccine adjuvant.