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Toll-like receptor 9 antagonizes antibody affinity maturation

Key events in T cell-dependent antibody responses, including affinity maturation, are dependent on the B cell’s presentation of antigen to helper T cells at critical check points in germinal center formation in secondary lymphoid organs. Here we show that Toll-like receptor 9 (TLR9) signaling blocke...

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Detalles Bibliográficos
Autores principales: Akkaya, Munir, Akkaya, Billur, Kim, Ann S., Miozzo, Pietro, Sohn, Haewon, Pena, Mirna, Roesler, Alexander S., Theall, Brandon P., Henke, Travis, Kabat, Juraj, Lu, Jinghua, Dorward, David W., Dahlstrom, Eric, Skinner, Jeff, Miller, Louis H., Pierce, Susan K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5839995/
https://www.ncbi.nlm.nih.gov/pubmed/29476183
http://dx.doi.org/10.1038/s41590-018-0052-z
Descripción
Sumario:Key events in T cell-dependent antibody responses, including affinity maturation, are dependent on the B cell’s presentation of antigen to helper T cells at critical check points in germinal center formation in secondary lymphoid organs. Here we show that Toll-like receptor 9 (TLR9) signaling blocked the ability of antigen-specific B cells to capture, process and present antigen and to activate antigen-specific helper T cells in vitro. In a mouse model in vivo and in a human clinical trial the TLR9 agonist, CpG, enhanced the magnitude of the antibody response to a protein vaccine but failed to promote affinity maturation. Thus, TLR9 signaling may enhance antibody titers at the expense of the ability of B cells to engage in germinal center events that are highly dependent on B cells’ antigen capture and presentation.