Gjurgjaj Altea, Conde Cecilia Domínguez
Human Technopole, Milan, Italy.
Eur J Immunol. 2025 Jun;55(6):e51233. doi: 10.1002/eji.202451233.
Autoimmune diseases encompass a range of conditions in which our own immune system reacts against molecules encoded by our own genome. This phenomenon is mediated by the action of antigen receptors expressed by T and B cells. Identifying the molecular events that trigger these responses as well as the effector cells that underlie them is at the heart of autoimmunity research. In this review, we discuss how single-cell multiomics techniques applied to healthy and patient tissues are shedding light on the mechanisms underpinning autoimmune conditions, specifically by identifying disease-associated cell states and cellular communication networks, including those linked to specific autoimmunity susceptibility genetic loci. Furthermore, we dive into the unprecedented resolution achieved in mapping autoreactive lymphocytes, a key component of autoimmune responses. We conclude with a perspective on key bottlenecks and promising future directions leveraging the latest advances in single-cell sequencing with orthogonal methods.
自身免疫性疾病包括一系列病症,在这些病症中,我们自身的免疫系统会对我们自身基因组编码的分子产生反应。这种现象是由T细胞和B细胞表达的抗原受体的作用介导的。确定引发这些反应的分子事件以及作为其基础的效应细胞是自身免疫研究的核心。在这篇综述中,我们讨论了应用于健康组织和患者组织的单细胞多组学技术如何揭示自身免疫性疾病的潜在机制,特别是通过识别与疾病相关的细胞状态和细胞通讯网络,包括那些与特定自身免疫易感性基因位点相关的网络。此外,我们深入探讨了在绘制自身反应性淋巴细胞(自身免疫反应的关键组成部分)图谱方面所取得的前所未有的分辨率。我们最后展望了利用单细胞测序的最新进展和正交方法的关键瓶颈及未来的发展方向。