Department of Medicine, Division of Molecular Medicine, University of São Paulo School of Medicine, São Paulo, Brazil; Laboratory of Medical Investigation 29, University of São Paulo School of Medicine, São Paulo, Brazil; Department of Pharmacy and Postgraduate Program of Health and Science, Federal University of Rio Grande do Norte, Natal, Brazil; Department of Immunology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil; Department of Clinical and Toxicological Analyses, School of Pharmaceutical Sciences, University of São Paulo, São Paulo, Brazil; Interunit Postgraduate Program on Bioinformatics, Institute of Mathematics and Statistics (IME), University of Sao Paulo (USP), Sao Paulo, Brazil.
Department of Nephrology and Internal Intensive Care Medicine, Charité University Hospital, Berlin, Germany; BIH Center for Regenerative Therapies (BCRT) and Berlin-Brandenburg School for Regenerative Therapies (BSRT), all Charité Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin Institute of Health, Berlin, Germany.
Autoimmun Rev. 2023 May;22(5):103310. doi: 10.1016/j.autrev.2023.103310. Epub 2023 Mar 10.
G protein-coupled receptors (GPCR) are involved in various physiological and pathophysiological processes. Functional autoantibodies targeting GPCRs have been associated with multiple disease manifestations in this context. Here we summarize and discuss the relevant findings and concepts presented in the biennial International Meeting on autoantibodies targeting GPCRs (the 4th Symposium), held in Lübeck, Germany, 15-16 September 2022. The symposium focused on the current knowledge of these autoantibodies' role in various diseases, such as cardiovascular, renal, infectious (COVID-19), and autoimmune diseases (e.g., systemic sclerosis and systemic lupus erythematosus). Beyond their association with disease phenotypes, intense research related to the mechanistic action of these autoantibodies on immune regulation and pathogenesis has been developed, underscoring the role of autoantibodies targeting GPCRs on disease outcomes and etiopathogenesis. The observation repeatedly highlighted that autoantibodies targeting GPCRs could also be present in healthy individuals, suggesting that anti-GPCR autoantibodies play a physiologic role in modeling the course of diseases. Since numerous therapies targeting GPCRs have been developed, including small molecules and monoclonal antibodies designed for treating cancer, infections, metabolic disorders, or inflammatory conditions, anti-GPCR autoantibodies themselves can serve as therapeutic targets to reduce patients' morbidity and mortality, representing a new area for the development of novel therapeutic interventions.
G 蛋白偶联受体(GPCR)参与多种生理和病理生理过程。在这种情况下,针对 GPCR 的功能性自身抗体与多种疾病表现有关。在这里,我们总结并讨论了 2022 年 9 月 15 日至 16 日在德国吕贝克举行的两年一次的针对 GPCR 的自身抗体国际会议(第四届研讨会)上提出的相关发现和概念。该研讨会的重点是这些自身抗体在各种疾病(如心血管、肾脏、感染(COVID-19)和自身免疫性疾病(如系统性硬化症和系统性红斑狼疮)中的作用的最新知识。除了与疾病表型的关联外,还针对这些自身抗体对免疫调节和发病机制的机制作用开展了大量研究,强调了针对 GPCR 的自身抗体在疾病结局和病因发病机制中的作用。这一观察结果反复强调,针对 GPCR 的自身抗体也可能存在于健康个体中,这表明针对 GPCR 的自身抗体在模拟疾病过程中发挥着生理作用。由于已经开发出许多针对 GPCR 的治疗方法,包括用于治疗癌症、感染、代谢紊乱或炎症的小分子和单克隆抗体,因此针对 GPCR 的自身抗体本身可以作为治疗靶点,以降低患者的发病率和死亡率,这代表了开发新的治疗干预措施的一个新领域。