Functional autoantibodies against G-protein coupled receptors in patients with persistent Long-COVID-19 symptoms
Item Type: | Article |
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Title: | Functional autoantibodies against G-protein coupled receptors in patients with persistent Long-COVID-19 symptoms |
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Creators Name: | Wallukat, G. and Hohberger, B. and Wenzel, K. and Fürst, J. and Schulze-Rothe, S. and Wallukat, A. and Hönicke, A.S. and Müller, J. |
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Abstract: | Impairment of health after overcoming the acute phase of COVID-19 is being observed more and more frequently. Here different symptoms of neurological and/or cardiological origin have been reported. With symptoms, which are very similar to the ones reported but are not caused by SARS-CoV-2, the occurrence of functionally active autoantibodies ((f)AABs) targeting G-protein coupled receptors (GPCR-(f)AABs) has been discussed to be involved. We, therefore investigated, whether GPCR-(f)AABs are detectable in 31 patients suffering from different Long-COVID-19 symptoms after recovery from the acute phase of the disease. The spectrum of symptoms was mostly of neurological origin (29/31 patients), including post-COVID-19 fatigue, alopecia, attention deficit, tremor and others. Combined neurological and cardiovascular disorders were reported in 17 of the 31 patients. Two recovered COVID-19 patients were free of follow-up symptoms. All 31 former COVID-19 patients had between 2 and 7 different GPCR-(f)AABs that acted as receptor agonists. Some of those GPCR-(f)AABs activate their target receptors which cause a positive chronotropic effect in neonatal rat cardiomyocytes, the read-out in the test system for their detection (bioassay for GPCR-(f)AAB detection). Other GPCR-(f)AABs, in opposite, cause a negative chronotropic effect on those cells. The positive chronotropic GPCR-(f)AABs identified in the blood of Long-COVID patients targeted the β(2)-adrenoceptor (β(2)-(f)AAB), the α1-adrenoceptor (α(1)-(f)AAB), the angiotensin II AT1-receptor (AT1-(f)AAB), and the nociceptin-like opioid receptor (NOC-(f)AAB). The negative chronotropic GPCR-(f)AABs identified targeted the muscarinic M(2)-receptor (M(2)-(f)AAB), the MAS-receptor (MAS-(f)AAB), and the ETA-receptor (ETA-(f)AAB). It was analysed which of the extracellular receptor loops was targeted by the autoantibodies. |
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Keywords: | Autoantibody, Autoimmunity, COVID-19, Fatigue, Post-Covid-19 Symptom, Long-COVID |
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Source: | Journal of Translational Autoimmunity |
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ISSN: | 2589-9090 |
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Publisher: | Elsevier |
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Volume: | 4 |
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Page Range: | 100100 |
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Date: | 16 April 2021 |
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Official Publication: | https://doi.org/10.1016/j.jtauto.2021.100100 |
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PubMed: | View item in PubMed |
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