Key result
BC 007 infusion neutralizes GPCR autoantibodies within 48 hours, alongside improved microcirculation and chronic fatigue.
Why the study?
Long-Covid syndrome is challenging to manage and is associated with impaired capillary microcirculation, chronic fatigue syndrome, and functional autoantibodies targeting G-protein-coupled receptors.
Does a single treatment with BC 007 improve capillary impairment and fatigue symptoms in a patient with long-Covid syndrome and GPCR-AAbs?
Case Report (n=1)
No
Does a single treatment with BC 007 improve capillary impairment and fatigue symptoms in a patient with long-Covid syndrome and GPCR-AAbs?
Answers are grounded in this paper and cite their sources.
Neutralization of GPCR-AAbs with BC 007 may improve capillary impairment, loss of taste, and chronic fatigue syndrome in patients with long-Covid syndrome.
Clinical features of Coronavirus disease 2019 (COVID-19) are caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). Acute infection management is a substantial healthcare issue, and the development of long-Covid syndrome (LCS) is extremely challenging for patients and physicians. It is associated with a variety of characteristics as impaired capillary microcirculation, chronic fatigue syndrome (CFS), proinflammatory cytokines, and functional autoantibodies targeting G-protein-coupled receptors (GPCR-AAbs). Here, we present a case report of successful healing of LCS with BC 007 (Berlin Cures, Berlin, Germany), a DNA aptamer drug with a high affinity to GPCR-AAbs that neutralizes these AAbs. A patient with a documented history of glaucoma, recovered from mild COVID-19, but still suffered from CFS, loss of taste, and impaired capillary microcirculation in the macula and peripapillary region. He was positively tested for various targeting GPCR-AAbs. Within 48 h after a single BC 007 treatment, GPCR-AAbs were functionally inactivated and remained inactive during the observation period of 4 weeks. This observation was accompanied by constant improvement of the fatigue symptoms of the patient, taste, and retinal capillary microcirculation. Therefore, the removal of GPCR-AAb might ameliorate the characteristics of the LCD, such as capillary impairment, loss of taste, and CFS.
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Hohberger et al. (2021) conducted a case report in Long-COVID syndrome (n=1). BC 007 vs. Pre-treatment baseline was evaluated on Neutralization of GPCR-AAbs, improvement in capillary microcirculation and fatigue symptoms. A single infusion of BC 007 neutralized functional GPCR autoantibodies within 48 hours, accompanied by continuous improvement in retinal capillary microcirculation, chronic fatigue, and loss of taste over 4 weeks.
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