Lajqi Trim, Köstlin-Gille Natascha, Bauer Reinhard, Zarogiannis Sotirios G, Lajqi Esra, Ajeti Valdrina, Dietz Stefanie, Kranig Simon A, Rühle Jessica, Demaj Ardian, Hebel Janine, Bartosova Maria, Frommhold David, Hudalla Hannes, Gille Christian
Department of Neonatology, Heidelberg University Children's Hospital, D-69120 Heidelberg, Germany.
Department of Neonatology, University of Tübingen, D-72076 Tübingen, Germany.
Biomedicines. 2023 Mar 2;11(3):766. doi: 10.3390/biomedicines11030766.
For almost nearly a century, memory functions have been attributed only to acquired immune cells. Lately, this paradigm has been challenged by an increasing number of studies revealing that innate immune cells are capable of exhibiting memory-like features resulting in increased responsiveness to subsequent challenges, a process known as trained immunity (known also as innate memory). In contrast, the refractory state of endotoxin tolerance has been defined as an immunosuppressive state of myeloid cells portrayed by a significant reduction in the inflammatory capacity. Both training as well tolerance as adaptive features are reported to be accompanied by epigenetic and metabolic alterations occurring in cells. While training conveys proper protection against secondary infections, the induction of endotoxin tolerance promotes repairing mechanisms in the cells. Consequently, the inappropriate induction of these adaptive cues may trigger maladaptive effects, promoting an increased susceptibility to secondary infections-tolerance, or contribute to the progression of the inflammatory disorder-trained immunity. This review aims at the discussion of these opposing manners of innate immune and non-immune cells, describing the molecular, metabolic and epigenetic mechanisms involved and interpreting the clinical implications in various inflammatory pathologies.
近一个世纪以来,记忆功能一直仅被归因于获得性免疫细胞。最近,这一范式受到了越来越多研究的挑战,这些研究表明先天免疫细胞能够表现出类似记忆的特征,从而导致对后续刺激的反应性增强,这一过程被称为训练免疫(也称为先天记忆)。相比之下,内毒素耐受的不应答状态被定义为髓样细胞的一种免疫抑制状态,其特征是炎症能力显著降低。据报道,训练和耐受这两种适应性特征都伴随着细胞中发生的表观遗传和代谢改变。虽然训练能对二次感染提供适当的保护,但内毒素耐受的诱导会促进细胞中的修复机制。因此,这些适应性信号的不适当诱导可能会引发适应不良效应,增加对二次感染耐受的易感性,或导致炎症性疾病——训练免疫的进展。这篇综述旨在讨论先天免疫细胞和非免疫细胞的这些相反方式,描述所涉及的分子、代谢和表观遗传机制,并解释其在各种炎症性疾病中的临床意义。