Medical Scientist Training Program, School of Medicine, Johns Hopkins University, Baltimore, MD, United States.
Ghost Lab, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, United States.
Front Immunol. 2023 Jan 18;14:1046300. doi: 10.3389/fimmu.2023.1046300. eCollection 2023.
The Danger Model predicts that there are some molecules that no immune system can ever be fully tolerant of, namely proteins that are only transiently expressed during times of stress, infection, or injury. Among these are the danger/alarm signals themselves. Accordingly, a fleeting autoantibody response to danger signals is expected during times when they are released. Depending on context, these autoantibodies may serve beneficial "housekeeping" functions by removing surplus danger signals from the circulation or, conversely, create an immunodeficiency. Here, we will focus on the Type 1 Interferons as examples of foreseeable targets for a transient autoantibody response, but the principles outlined should hold for other danger-associated molecules as well.
危险模型预测,有些分子是免疫系统永远无法完全耐受的,即只有在应激、感染或损伤时才短暂表达的蛋白质。其中包括危险/警报信号本身。因此,在释放这些信号时,预计会短暂地出现针对危险信号的自身抗体反应。根据具体情况,这些自身抗体可能通过从循环中清除多余的危险信号来发挥有益的“管家”功能,或者相反,导致免疫缺陷。在这里,我们将以 I 型干扰素为例,说明对短暂自身抗体反应的可预见靶标,但概述的原则也应适用于其他与危险相关的分子。