A novel mouse model for tracking the fate of CXCR5-expressing T cells

Abstract

The germinal center (GC) reaction, a critical process in the humoral immune response, requires follicular helper T (Tfh) cells. Tfh cells express the master transcription factor Bcl6 and chemokine receptor CXCR5, which enable them to migrate from the T cell zone to B cell follicles and interact with GC B cells. However, CXCR5 is downregulated when Tfh cells become memory cells. Therefore, it is difficult to track Tfh cells continuously in vivo. In this study, we generated a mouse strain, Cxcr5^CreERT2R26^Tomato, in which the fluorescent protein tdTomato is inducibly expressed in CXCR5⁺ cells by tamoxifen administration. After the oral administration of tamoxifen, most Tfh cells in Peyer's patches (PP) from Cxcr5^CreERT2R26^Tomato mice were tdTomato⁺. To track antigen-specific Tfh cells in vivo, OVA-specific OT-II T cells derived from Cxcr5^CreERT2R26^Tomato mice were transferred to wild-type mice, and the recipient mice were immunized with OVA followed by tamoxifen administration. CXCR5⁺ T cells became tdTomato⁺ and were mainly located in B cell follicles and GC areas 8 days after immunization. Four weeks after immunization, tdTomato⁺ OT-II T cells migrated from B cell follicles to the T-B border area and T cell zone after CXCR5 downregulation and CCR7 upregulation. These results indicate that Cxcr5^CreERT2R26^Tomato mice are a useful tool for studying the cell fate of differentiated Tfh cells in vivo and therefore have implications for the development of therapeutic strategies for infectious and autoimmune diseases.

Keywords: CXCR5; Follicular helper T cells; Humoral immunity; Memory T cells.