Autoantibodies targeting G protein-coupled receptors: An evolving history in autoimmunity. Report of the 4th international symposium

Otávio Cabral-Marques*, Guido Moll, Rusan Catar, Beate Preuß, Lukas Bankamp, Ann Christin Pecher, Joerg Henes, Reinhild Klein, A. S. Kamalanathan, Reza Akbarzadeh, Wieke van Oostveen, Bettina Hohberger, Matthias Endres, Bryan Koolmoes, Nivine Levarht, Rudmer Postma, Vincent van Duinen, Anton Jan van Zonneveld, Jeska de Vries-Bouwstra, Cynthia FehresFlorian Tran, Fernando Yuri Nery do Vale, Kamilla Batista da Silva Souza, Igor Salerno Filgueiras, Lena F. Schimke, Gabriela Crispim Baiocchi, Gustavo Cabral de Miranda, Dennyson Leandro Mathias da Fonseca, Paula Paccielli Freire, Alexander M. Hackel, Hanna Grasshoff, Anja Kerstein-Stähle, Antje Müller, Ralf Dechend, Xinhua Yu, Frank Petersen, Franziska Sotzny, Thomas P. Sakmar, Hans D. Ochs, Kai Schulze-Forster, Harald Heidecke, Carmen Scheibenbogen, Yehuda Shoenfeld, Gabriela Riemekasten*

*Korrespondierende/r Autor/-in für diese Arbeit

Abstract

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.

OriginalspracheEnglisch
Aufsatznummer103310
ZeitschriftAutoimmunity Reviews
Jahrgang22
Ausgabenummer5
Seiten (von - bis)103310
ISSN1568-9972
DOIs
PublikationsstatusVeröffentlicht - 05.2023

Fördermittel

We thank the São Paulo State Research Support Foundation (FAPESP grants: 2018/18886-9, 2020/01688-0, and 2020/07069-0 to OCM, 2019/14526-0 and 2020/05146-7 to GCM, 2020/09146 to PPF, 2020/16246-2 to DLMF, and 2020/07972-1 to GCB). This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior – Brasil (CAPES) – Finance Code 001, Grants to KBSS and FYNV. We acknoledge the National Council for Scientific and Technological Development (CNPq) , Brazil (grants: 309482/2022-4 to OCM and to 102430/2022-5 to LFS) G.M.'s contributions were made possible by the German Research Foundation / Deutsche Forschungsgemeinschaft (DFG; EXPAND-PD CA2816/1-1) and German Federal Ministry of Education and Research (BMBF) funding through the BSRT (GSC203) and BCRT. In addition, this project has received funding from the European Union's Horizon 2020 research and innovation program under grant agreements No 733006 (PACE) and No 779293 (HIPGEN). Contributions of R.C. were made possible by funding from the DFG project #394046635, subproject A03, as part of CRC 1365 and EXPAND-PD; CA2816/1-1. Furthermore, GR, HG, and FT received funding from the excellence cluster precision medicine in chronic inflammation, Mesinflame funding to GR, and IMMME funding to GR, CS, and FS. Funding by the BMBF, German Center for Lung Research (DZL), and by the DFG RTG 2633 “Autoimmune Pre-Disease”; Project B3 enabled contributions by X.Y. and F.P. We acknowledge all sponsors of the 4th RAB Symposium in Lübeck: Deutsche Forschungsgemeinschaft (DFG), CellTrend, Abbvie, Galápagos, Janssen Pharmaceutical Companies, AstraZeneca, Boehringer Ingelheim, Biogen, Bristol Myers Squibb, EUROIMMUN, GlaxoSmithKline (GSK), and UCB Biopharma.

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

  1. SDG 3 – Gesundheit und Wohlergehen
    SDG 3 – Gesundheit und Wohlergehen

Strategische Forschungsbereiche und Zentren

  • Forschungsschwerpunkt: Infektion und Entzündung - Zentrum für Infektions- und Entzündungsforschung Lübeck (ZIEL)

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