The integrated stress response pathway controls cytokine production in tissue-resident memory CD4+ T cells

Tissue-resident memory T (T<sub>RM</sub>) cells are a specialized T cell population that reside in tissues and provide a rapid protective response upon activation. Here, we showed that human and mouse CD4<sup>+</sup> T<sub>RM</sub> cells existed in a poised state and stored messenger RNAs encoding proinflammatory cytokines without protein production. At steady state, cytokine mRNA translation in T<sub>RM</sub> cells was suppressed by the integrated stress response (ISR) pathway. Upon activation, the central ISR regulator, eIF2α, was dephosphorylated and stored cytokine mRNA was translated for immediate cytokine production. Genetic or pharmacological activation of the ISR-eIF2α pathway reduced cytokine production and ameliorated autoimmune kidney disease in mice. Consistent with these results, the ISR pathway in CD4<sup>+</sup> T<sub>RM</sub> cells was downregulated in patients with immune-mediated diseases of the kidney and the intestine compared to healthy controls. Our results indicated that stored cytokine mRNA and translational regulation in CD4<sup>+</sup> T<sub>RM</sub> cells facilitate rapid cytokine production during local immune response.

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Publication Details

Journal
Nature Immunology
Published
2025-03-06
DOI
https://doi.org/10.1038/s41590-025-02105-x
Citations
27
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
21.53

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article

The integrated stress response pathway controls cytokine production in tissue-resident memory CD4+ T cells

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27 citations
Nature Immunology
Immune Cell Function and Interaction
21.53
article

The integrated stress response pathway controls cytokine production in tissue-resident memory CD4+ T cells

Pauline Ginsberg, Hans‐Joachim Paust, Roland Dahlem, Immo Prinz, Hans‐Willi Mittrücker, Zoya Ignatova, Nicola Gagliani, Christian F. Krebs, Anett Peters, Anna Kaffke, Ulf Panzer, Yu Zhao, Björn‐Philipp Diercks, Philipp Gild, Jan-Hendrik Riedel, Nariaki Asada, Tobias B. Huber, Sarada Das, Robin Khatri, Jonas Engeßer, Huiying Wang, Ning Song, Jan-Eric Turner
article en
27 citations

Abstract

Tissue-resident memory T (T<sub>RM</sub>) cells are a specialized T cell population that reside in tissues and provide a rapid protective response upon activation. Here, we showed that human and mouse CD4<sup>+</sup> T<sub>RM</sub> cells existed in a poised state and stored messenger RNAs encoding proinflammatory cytokines without protein production. At steady state, cytokine mRNA translation in T<sub>RM</sub> cells was suppressed by the integrated stress response (ISR) pathway. Upon activation, the central ISR regulator, eIF2α, was dephosphorylated and stored cytokine mRNA was translated for immediate cytokine production. Genetic or pharmacological activation of the ISR-eIF2α pathway reduced cytokine production and ameliorated autoimmune kidney disease in mice. Consistent with these results, the ISR pathway in CD4<sup>+</sup> T<sub>RM</sub> cells was downregulated in patients with immune-mediated diseases of the kidney and the intestine compared to healthy controls. Our results indicated that stored cytokine mRNA and translational regulation in CD4<sup>+</sup> T<sub>RM</sub> cells facilitate rapid cytokine production during local immune response.

Nature ImmunologyVol. 26(4)
Universität Hamburg (DE), University Medical Center Hamburg-Eppendorf (DE)
Deutsche Forschungsgemeinschaft, Servier, Japan Society for the Promotion of Science
Openalex Percentile: Top 0%
Immune Cell Function and Interaction
21.53
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