Institute of Infectious Disease and Immunology, Stritch School of Medicine, Loyola University Chicago, USA.
Department of Microbiology and Immunology, Stritch School of Medicine, Loyola University Chicago, USA.
Cytokine. 2018 Nov;111:454-459. doi: 10.1016/j.cyto.2018.05.036. Epub 2018 Jun 6.
TNF is a multifunctional cytokine that is critical to host defense against pathogens but can also drive the pathophysiology of inflammatory diseases. Inhibition of TNF occasionally causes exacerbation of some autoimmune diseases, suggesting a role for TNF in the regulation of immune homeostasis. Here, we demonstrate that human peripheral blood CD4CD25Foxp3 regulatory T cells (Tregs) express membrane-bound TNF, a potent activator of the type 2 TNF receptor. While the type 1 TNF receptor can cause cell death and is expressed ubiquitously, the type 2 receptor promotes cell growth and its expression is limited mainly to immune and endothelial cells. When autocrine TNF is blocked in an in vitro culture without IL-2, activated Tregs stop proliferating. These data indicate a novel role for TNF as a Treg-derived autocrine growth factor.
肿瘤坏死因子(TNF)是一种多功能细胞因子,对于宿主抵抗病原体至关重要,但也可驱动炎症性疾病的病理生理学过程。TNF 的抑制偶尔会导致某些自身免疫性疾病的恶化,这表明 TNF 在免疫稳态的调节中发挥作用。在这里,我们证明人类外周血 CD4+CD25+Foxp3+调节性 T 细胞(Treg)表达膜结合 TNF,这是一种 2 型 TNF 受体的有效激活物。虽然 1 型 TNF 受体可导致细胞死亡且广泛表达,但 2 型受体促进细胞生长,其表达主要局限于免疫细胞和内皮细胞。当在没有 IL-2 的体外培养中阻断自分泌 TNF 时,激活的 Treg 停止增殖。这些数据表明 TNF 作为 Treg 衍生的自分泌生长因子发挥了新的作用。