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Germinal center–dependent and –independent memory B cells produced throughout the immune response

Memory B cells comprise a heterogenous group of cells that differ in origin and phenotype. During the early phases of the immune response, activated B cells can differentiate into IgM-expressing memory cells, short-lived plasma cells, or seed germinal centers (GCs). The memory compartment is subsequ...

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Detalles Bibliográficos
Autores principales: Viant, Charlotte, Wirthmiller, Tobias, ElTanbouly, Mohamed A., Chen, Spencer T., Cipolla, Melissa, Ramos, Victor, Oliveira, Thiago Y., Stamatatos, Leonidas, Nussenzweig, Michel C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8193567/
https://www.ncbi.nlm.nih.gov/pubmed/34106207
http://dx.doi.org/10.1084/jem.20202489
Descripción
Sumario:Memory B cells comprise a heterogenous group of cells that differ in origin and phenotype. During the early phases of the immune response, activated B cells can differentiate into IgM-expressing memory cells, short-lived plasma cells, or seed germinal centers (GCs). The memory compartment is subsequently enriched by B cells that have been through several rounds of division and selection in the GC. Here, we report on the use of an unbiased lineage-tracking approach to explore the origins and properties of memory B cell subsets in mice with an intact immune system. We find that activated B cells continue to differentiate into memory B cells throughout the immune response. When defined on the basis of their origins, the memory B cells originating from activated B cells or GCs differ in isotype and overall gene expression, somatic hypermutation, and their affinity for antigen.