Noé Rodríguez-Rodríguez, Florencia Rosetti, José C Crispín
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引用次数: 0
Abstract
Activated CD8+ T cells directly kill target cells. Therefore, the regulation of their function is central to avoiding immunopathology. Mechanisms that curb effector functions in CD4+ and CD8+ T cells are mostly shared, yet important differences occur. Here, we focus on the control of CD8+ T cell activity and discuss the importance of a poorly understood aspect of tolerance that directly impairs engagement of target cells: the downregulation of CD8. We contextualize this process and propose that it represents a key element during CD8+ T cell modulation.
活化的 CD8+ T 细胞可直接杀死靶细胞。因此,对其功能的调控是避免免疫病理的关键。抑制 CD4+ 和 CD8+ T 细胞效应功能的机制大多是相同的,但也存在重要差异。在这里,我们将重点放在对 CD8+ T 细胞活性的控制上,并讨论耐受性的一个鲜为人知的方面的重要性,它直接损害了靶细胞的参与:CD8 的下调。我们对这一过程进行了背景分析,并提出它是 CD8+ T 细胞调节过程中的一个关键因素。
期刊介绍:
Trends in Immunology serves as a vital platform for tracking advancements across various areas of immunology, offering concise reviews and hypothesis-driven viewpoints in each issue. With additional sections providing comprehensive coverage, the journal offers a holistic view of immunology. This broad perspective makes it an invaluable resource for researchers, educators, and students, facilitating the connection between basic and clinical immunology. Recognized as one of the top monthly review journals in its field, Trends in Immunology is highly regarded by the scientific community.