Yassini Nima, Goljat Eva, Panetti Camilla, Rath Matthias, Joller Nicole
Department of Quantitative Biomedicine, University of Zurich, Zurich, Switzerland.
Center for Human Immunology, University of Zurich, Zurich, Switzerland.
Eur J Immunol. 2025 Sep;55(9):e70054. doi: 10.1002/eji.70054.
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.
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。