Impact of immunoadsorption on autoantibodies and physical performance in post-COVID patients: a prospective exploratory study of 18 participants.

Impact of immunoadsorption on autoantibodies and physical performance in post-COVID patients: a prospective exploratory study of 18 participants.

Publication date: Aug 11, 2026

Autoantibodies against β-adrenergic and muscarinic acetylcholine receptors are said to play a role in the pathophysiology of post-COVID syndrome. To date, only a limited number of studies have investigated the effectiveness of immunoadsorption. This prospective exploratory study investigates the effectiveness of immunoadsorption by assessing reductions in autoantibody levels and improvements in physical performance. In a prospective exploratory clinical trial, 18 patients with post-COVID syndrome and elevated levels of antibodies against β1/β2-adrenergic receptors and/or M3/M4-muscarinic acetylcholine receptors were treated with a course of five consecutive immunoadsorption sessions. Clinical assessments, objective functional performance tests (e. g., step counters), laboratory parameters, and self-reported performance were performed during the study. A total of 15 women and 3 men were included in the study. Immunoadsorption was well tolerated. All participants showed a significant reduction in circulating antibodies against β1/β2-adrenergic receptors and M3/M4-muscarinic acetylcholine receptors; however, these levels returned to baseline within the following 3 to 6 months. Objective determinations of physical performance showed no significant improvement following immunoadsorption. Self-reported evaluation revealed a slight improvement in pain and fatigue. However, the correlation analysis failed to demonstrate a significant association between changes in autoantibody levels and subjectively perceived symptoms. Immunoadsorption was safe and resulted in a short-term, significant reduction in measured autoantibodies. However, there were no improvements in objectively measured performance. Our results indicate that immunoadsorption is not an effective approach for patients with post-COVID syndrome.

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Concepts Keywords
Covid Adrenergic receptors
Immunoadsorption Autoantibodies
M4 COVID-19
Months Immunoadsorption
Women Muscarinic receptors
Post-COVID

Semantics

Type Source Name
pathway REACTOME Muscarinic acetylcholine receptors
disease MESH syndrome
disease MESH included
disease MESH pain
disease MESH fatigue
disease MESH Infection
disease MESH Infectious Diseases
drug DRUGBANK Indoleacetic acid
drug DRUGBANK Choline
disease MESH COVID 19
drug DRUGBANK Stavudine
disease MESH Long COVID
disease MESH dyspnea
disease MESH tachycardia
disease MESH cognitive impairments
disease MESH Myalgic Encephalomyelitis
disease MESH hypercoagulability
disease MESH inflammation
drug DRUGBANK Coenzyme M
drug DRUGBANK Cysteamine
disease MESH sid
drug DRUGBANK Imidacloprid
disease MESH hepatitis
disease MESH Lyme disease
disease MESH tuberculosis
pathway KEGG Tuberculosis
disease MESH EBV infection
disease MESH cardiovascular diseases
disease MESH neurological disorders
disease MESH multiple sclerosis
drug DRUGBANK Heparin
disease MESH ACD
drug DRUGBANK Calcium
disease MESH body weight
disease MESH bleeding
drug DRUGBANK Etoperidone
disease MESH ers
drug DRUGBANK Chorionic Gonadotropin (Human)
disease MESH hCG
drug DRUGBANK Trestolone
disease MESH capa
drug DRUGBANK Methionine
disease MESH headaches
disease MESH muscle pain

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