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CD4 T细胞在经典T细胞激活后获得固有能力。

CD4 T Cells Acquire Innate Capability Upon Classical T Cell Activation.

作者信息

Yassini Nima, Goljat Eva, Panetti Camilla, Rath Matthias, Joller Nicole

机构信息

Department of Quantitative Biomedicine, University of Zurich, Zurich, Switzerland.

Center for Human Immunology, University of Zurich, Zurich, Switzerland.

出版信息

Eur J Immunol. 2025 Sep;55(9):e70054. doi: 10.1002/eji.70054.

Abstract

Memory T cells, a sizable compartment of the mature immune system, enable enhanced responses upon re-infection with the same pathogen. We have recently shown that virus-experienced innate acting T (T) cells can modulate infectious or autoimmune diseases through TCR-independent IFN-γ production. However, how these cells arise remains unclear. Here, we show that CD4 T cells are present in various disease settings hinting towards a disease-agnostic nature. TCR stimulation and CD28 co-stimulation are sufficient to induce naïve murine and human CD4 T cells to become capable of cytokine-mediated, TCR-independent IFN-γ responses. In true T fashion, adoptive transfer of in vitro-induced T cells in mice yielded a TCR-independent IFN-γ response during the innate phase of a Legionella pneumophila infection. Our data thus shows that CD4 T cells are more ubiquitous than anticipated and could therefore be involved in more settings than expected.

摘要

记忆性T细胞是成熟免疫系统的一个重要组成部分,能在再次感染相同病原体时产生更强的反应。我们最近发现,经历过病毒感染的固有作用T(Ti)细胞可通过不依赖TCR的γ干扰素产生来调节感染性疾病或自身免疫性疾病。然而,这些细胞是如何产生的仍不清楚。在此,我们表明CD4 T细胞存在于各种疾病环境中,这表明其具有与疾病无关的特性。TCR刺激和CD28共刺激足以诱导未成熟的小鼠和人类CD4 T细胞产生细胞因子介导的、不依赖TCR的γ干扰素反应。以真正的Ti细胞方式,将体外诱导的Ti细胞过继转移到小鼠体内,在嗜肺军团菌感染的固有阶段产生了不依赖TCR的γ干扰素反应。因此,我们的数据表明,CD4 T细胞比预期的更为普遍,因此可能参与比预期更多的疾病环境。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85af/12419137/9f15726dad18/EJI-55-e70054-g001.jpg

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