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How individual T cells compete for and respond to IL-2 at the molecular level, and, as a consequence, how this shapes population dynamics and the selection of high-affinity clones is still poorly understood. Here we describe how the RNA binding protein ZFP36L1, acts as a sensor of TCR affinity to promote clonal expansion of high-affinity CD8 T cells. As part of an incoherent feed-forward loop, ZFP36L1 has a nonredundant role in suppressing multiple negative regulators of cytokine signaling and mediating a selection mechanism based on competition for IL-2. We suggest that ZFP36L1 acts as a sensor of antigen affinity and establishes the dominance of high-affinity T cells by installing a hierarchical response to IL-2.

Original publication

DOI

10.1002/eji.202350700

Type

Journal article

Journal

European journal of immunology

Publication Date

02/2024

Volume

54

Addresses

The Babraham Institute, Babraham Research Campus, Cambridge, United Kingdom.

Keywords

CD8-Positive T-Lymphocytes, Clone Cells, Receptors, Antigen, T-Cell, Interleukin-2, Cytokines