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Follicular Regulatory T Cells Can Access the Germinal Center Independently of CXCR5.

ABSTRACT: The germinal center (GC) response is critical for generating high-affinity humoral immunity and immunological memory, which forms the basis of successful immunization. Control of the GC response is thought to require follicular regulatory T (Tfr) cells, a subset of suppressive Foxp3⁺ regulatory T cells located within GCs. Relatively little is known about the exact role of Tfr cells within the GC and how they exert their suppressive function. A unique feature of Tfr cells is their reported CXCR5-dependent localization to the GC. Here, we show that the lack of CXCR5 on Foxp3⁺ regulatory T cells results in a reduced frequency, but not an absence, of GC-localized Tfr cells. This reduction in Tfr cells is not sufficient to alter the magnitude or output of the GC response. This demonstrates that additional, CXCR5-independent mechanisms facilitate Treg cell homing to the GC.

SUBMITTER: Vanderleyden I

PROVIDER: S-EPMC6988108 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Foxp3+ follicular regulatory T cells control the germinal center response.

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Human T follicular helper clones seed the germinal center-resident regulatory pool.

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