PTPN22 mediates delayed negative feedback of T cell activation by forming an inhibitory signaling complex

PTPN22 is a cytosolic tyrosine phosphatase expressed in immune cells that negatively regulates T cell receptor (TCR) signaling and implicated in autoimmune diseases through a common (R620W) variant. The molecular mechanisms by which PTPN22 modulates TCR activation remain incompletely understood. Here we show that upon T cell activation, PTPN22 forms delayed clusters at TCR microclusters (MCs) alongside Csk, STS-1 and PSTPIP, constituting a feedback inhibitory complex. Using imaging analyses, MS, and knockout mouse models, we demonstrate that this complex functions as a delayed negative regulation of TCR signaling, and that autoimmune-associated PTPN22 (R620W) mutant exhibits reduced binding to Csk and STS-1, impairing complex formation. Consequently, T cells expressing the mutant display enhanced cytokine production and immune responses. These findings reveal cooperative inhibitory mechanism involving PTPN22 and its partners that modulates T cell activation, providing insights into how PTPN22 variants contribute to autoimmune disease susceptibility.

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Journal
International Immunology
Published
2026-09-25
DOI
https://doi.org/10.1093/intimm/dxag050
Primary Topic
Diabetes and associated disorders
Type
article
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article

PTPN22 mediates delayed negative feedback of T cell activation by forming an inhibitory signaling complex

Natsuko Tanimura, Akiko Soneda Hashimoto, Yusuke Kawashima, Natsumi Yoneda et al.
International Immunology
Diabetes and associated disorders
article

PTPN22 mediates delayed negative feedback of T cell activation by forming an inhibitory signaling complex

Natsuko Tanimura, Akiko Soneda Hashimoto, Yusuke Kawashima, Natsumi Yoneda, Takashi Saito, Osamu Ohara, Machie Sakuma, Manabu Nakayama, Haruhiko Koseki, Bernard Malissen
article en

Abstract

PTPN22 is a cytosolic tyrosine phosphatase expressed in immune cells that negatively regulates T cell receptor (TCR) signaling and implicated in autoimmune diseases through a common (R620W) variant. The molecular mechanisms by which PTPN22 modulates TCR activation remain incompletely understood. Here we show that upon T cell activation, PTPN22 forms delayed clusters at TCR microclusters (MCs) alongside Csk, STS-1 and PSTPIP, constituting a feedback inhibitory complex. Using imaging analyses, MS, and knockout mouse models, we demonstrate that this complex functions as a delayed negative regulation of TCR signaling, and that autoimmune-associated PTPN22 (R620W) mutant exhibits reduced binding to Csk and STS-1, impairing complex formation. Consequently, T cells expressing the mutant display enhanced cytokine production and immune responses. These findings reveal cooperative inhibitory mechanism involving PTPN22 and its partners that modulates T cell activation, providing insights into how PTPN22 variants contribute to autoimmune disease susceptibility.

International Immunology
MSD K.K. (Japan) (JP), Centre d’Immunologie de Marseille-Luminy (FR), Kazusa DNA Research Institute (JP), RIKEN Center for Integrative Medical Sciences (JP)
Good health and well-being
Openalex Percentile: Top 12%
Diabetes and associated disorders
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PTPN22 mediates delayed negative feedback of T cell activation by forming an inhibitory signaling complex — Natsuko Tanimura, Akiko Soneda Hashimoto, et al. · International Immunology (2026) | TGRS Research Map | TGRS