J Clin Invest. 2022 Aug 15;132(16). doi: 10.1172/JCI162170.
Autoimmunity has long been regarded as the polar opposite of immunodeficiency, but clinical and experimental evidence refute this notion. Indeed, numerous inborn or acquired immunodeficiency syndromes are characterized by the development of autoimmune complications in the setting of deficient immune defenses against microbial pathogens. Appreciation that much of the daily business of a healthy immune system is the avoidance of potentially harmful responses to innocuous environmental antigens or components of the host organism helps provide a context for these observations. In this issue of the JCI, Abt and colleagues report on purine nucleoside phosphorylase (PNP) deficiency, exploring the basis for the autoimmune complications that develop in this particular form of T cell immune deficiency and assigning a key role for overactivation of TLR7.
自身免疫性疾病长期以来被认为与免疫缺陷完全相反,但临床和实验证据驳斥了这一观点。事实上,许多先天或获得性免疫缺陷综合征的特征是在对微生物病原体的免疫防御不足的情况下发展出自身免疫性并发症。认识到健康免疫系统的日常工作很大程度上是避免对无害的环境抗原或宿主生物成分产生潜在有害的反应,有助于为这些观察结果提供一个背景。在本期 JCI 中,Abt 及其同事报告了嘌呤核苷磷酸化酶(PNP)缺乏症,探讨了这种特定形式的 T 细胞免疫缺陷中发生的自身免疫性并发症的基础,并确定 TLR7 的过度激活起关键作用。