Opposing Roles of Type I Interferons in Cancer Immunity.

IF 28.4 1区 医学 Q1 PATHOLOGY
Giselle M Boukhaled, Shane Harding, David G Brooks
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引用次数: 64

Abstract

The immune system is tasked with identifying malignant cells to eliminate or prevent cancer spread. This involves a complex orchestration of many immune cell types that together recognize different aspects of tumor transformation and growth. In response, tumors have developed mechanisms to circumvent immune attack. Type I interferons (IFN-Is) are a class of proinflammatory cytokines produced in response to viruses and other environmental stressors. IFN-Is are also emerging as essential drivers of antitumor immunity, potently stimulating the ability of immune cells to eliminate tumor cells. However, a more complicated role for IFN-Is has arisen, as prolonged stimulation can promote feedback inhibitory mechanisms that contribute to immune exhaustion and other deleterious effects that directly or indirectly permit cancer cells to escape immune clearance. We review the fundamental and opposing functions of IFN-Is that modulate tumor growth and impact immune function and ultimately how these functions can be harnessed for the design of new cancer therapies.

I型干扰素在肿瘤免疫中的对立作用。
免疫系统的任务是识别恶性细胞,以消除或防止癌症扩散。这涉及到许多免疫细胞类型的复杂协调,它们共同识别肿瘤转化和生长的不同方面。作为回应,肿瘤已经发展出了规避免疫攻击的机制。I型干扰素(IFN-Is)是一类促炎细胞因子,在对病毒和其他环境应激源的反应中产生。IFN-Is也成为抗肿瘤免疫的重要驱动因素,它能有效地刺激免疫细胞消除肿瘤细胞的能力。然而,IFN-Is的一个更复杂的作用已经出现,因为长时间的刺激可以促进反馈抑制机制,导致免疫衰竭和其他有害影响,直接或间接地允许癌细胞逃避免疫清除。我们回顾了IFN-Is调节肿瘤生长和影响免疫功能的基本功能和相反功能,以及最终如何利用这些功能设计新的癌症治疗方法。
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来源期刊
CiteScore
62.60
自引率
0.00%
发文量
40
期刊介绍: The Annual Review of Pathology: Mechanisms of Disease is a scholarly journal that has been published since 2006. Its primary focus is to provide a comprehensive overview of recent advancements in our knowledge of the causes and development of significant human diseases. The journal places particular emphasis on exploring the current and evolving concepts of disease pathogenesis, as well as the molecular genetic and morphological changes associated with various diseases. Additionally, the journal addresses the clinical significance of these findings. In order to increase accessibility and promote the broad dissemination of research, the current volume of the journal has transitioned from a gated subscription model to an open access format. This change has been made possible through the Annual Reviews' Subscribe to Open program, which allows all articles published in this volume to be freely accessible to readers. As part of this transition, all articles in the journal are published under a Creative Commons Attribution (CC BY) license, which encourages open sharing and use of the research.
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