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Updated: Sep 22, 2025

Evaluation of T Follicular Helper Cells and Germinal Center Response During Influenza A Virus Infection in Mice
Published on: June 27, 2020
T Cell Specific BOB.1/OBF.1 Expression Promotes Germinal Center Response and T Helper Cell Differentiation.
Annika C Betzler1, Jasmin Ezić1, Tsima Abou Kors1
1Department of Oto-Rhino-Laryngology, Ulm University Medical Center, Ulm, Germany.
The transcriptional co-activator BOB.1/OBF.1 is crucial for germinal center (GC) formation, impacting both B and T cells. Its absence in T cells, particularly follicular T helper (TFH) cells, impairs GC reactions.
Area of Science:
- Immunology
- Molecular Biology
- Cell Biology
Background:
- The transcriptional co-activator BOB.1/OBF.1 is expressed in both B and T lymphocytes.
- Conventional BOB.1/OBF.1 deficient mice exhibit a complete absence of germinal centers (GCs), primarily attributed to B cell defects.
- The specific role of BOB.1/OBF.1 in T cells regarding the GC reaction remains unclear.
Purpose of the Study:
- To investigate the in vivo function of BOB.1/OBF.1 in CD4+ T and follicular T helper (TFH) cell subpopulations.
- To determine the contribution of T cell-specific BOB.1/OBF.1 expression to the GC reaction.
Main Methods:
- Conditional mutagenesis was employed to delete BOB.1/OBF.1 in CD4+ T and TFH cells.
- Experiments were conducted in the presence of immunocompetent B lymphocytes.
Main Results:
- Deletion of BOB.1/OBF.1 in CD4+ T cells and TFH cells led to impaired GC formation.
- This indicates that the defective GC reaction in conventional BOB.1/OBF.1-deficient mice is not solely due to B cell defects.
- BOB.1/OBF.1 is essential for the differentiation of T helper (TH) cell subsets, especially TFH cells.
Conclusions:
- BOB.1/OBF.1 plays a significant role in T cells, contributing to the GC reaction.
- The findings necessitate a re-evaluation of the exclusive attribution of GC defects to B cell compartments in BOB.1/OBF.1 deficiency.
- BOB.1/OBF.1 is critical for TFH cell differentiation and function.
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