Germinal center formation is resilient to CD69 deletion on T follicular helper cells

T follicular helper (T<sub>FH</sub>) cells are a helper T-cell subset that is defined by their localisation to B-cell areas of secondary lymphoid tissues, enabling them to provide their B-cell helper function. Precursors of T<sub>FH</sub> cells migrate to the B-cell follicles by upregulating CXCR5 and downregulating CCR7, a process that can be blocked by S1PR1 overexpression. T<sub>FH</sub> cells and their precursors also express the early activation antigen CD69, which is a negative regulator of S1PR1. In this study, we tested the hypothesis that CD69 expression by T<sub>FH</sub> cells is important for their differentiation and localisation after immunization. Genetic deletion of CD69 on T<sub>FH</sub> cells and a proportion of their precursors did not alter their formation, nor their ability to support high-affinity B-cell responses. This demonstrates that although CD69 is expressed highly on T<sub>FH</sub> cells, it is not necessary for their formation or their B-cell helper functions in lymph nodes (LNs).

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Publication Details

Journal
Immunology and Cell Biology
Published
2025-08-04
DOI
https://doi.org/10.1111/imcb.70051
Primary Topic
T-cell and B-cell Immunology
Type
article
Field-Weighted Citation Impact
0.00

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article

Germinal center formation is resilient to CD69 deletion on T follicular helper cells

Silvia Innocentin, Louise M. C. Webb, Stéphane M. Guillaume, Michelle A. Linterman et al.
Immunology and Cell Biology
T-cell and B-cell Immunology
article

Germinal center formation is resilient to CD69 deletion on T follicular helper cells

Silvia Innocentin, Louise M. C. Webb, Stéphane M. Guillaume, Michelle A. Linterman, Adrian Liston, William S. Foster, Helena A Carslaw
article en

Abstract

T follicular helper (T<sub>FH</sub>) cells are a helper T-cell subset that is defined by their localisation to B-cell areas of secondary lymphoid tissues, enabling them to provide their B-cell helper function. Precursors of T<sub>FH</sub> cells migrate to the B-cell follicles by upregulating CXCR5 and downregulating CCR7, a process that can be blocked by S1PR1 overexpression. T<sub>FH</sub> cells and their precursors also express the early activation antigen CD69, which is a negative regulator of S1PR1. In this study, we tested the hypothesis that CD69 expression by T<sub>FH</sub> cells is important for their differentiation and localisation after immunization. Genetic deletion of CD69 on T<sub>FH</sub> cells and a proportion of their precursors did not alter their formation, nor their ability to support high-affinity B-cell responses. This demonstrates that although CD69 is expressed highly on T<sub>FH</sub> cells, it is not necessary for their formation or their B-cell helper functions in lymph nodes (LNs).

Immunology and Cell BiologyVol. 103(9)
Babraham Institute (GB), University of Cambridge (GB)
UK Research and Innovation, European Commission, Directorate for Biological Sciences, Horizon 2020 Framework Programme, Engineering and Physical Sciences Research Council, Biotechnology and Biological Sciences Research Council
Openalex Percentile: Top 78%
T-cell and B-cell Immunology
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Germinal center formation is resilient to CD69 deletion on T follicular helper cells — Silvia Innocentin, Louise M. C. Webb, et al. · Immunology and Cell Biology (2025) | TGRS Research Map | TGRS