関連する実験動画
Updated: Jan 13, 2026

Measurement of Antibody Effects on Cellular Function of Isolated Cardiomyocytes
Published on: March 8, 2013
進行性拡張型心筋症における免疫吸着療法の成功:症例報告
Rendan Zhang1,2, Lvwen Ning1,2, Ying Liu1,2
1Department of Geriatrics, Shenzhen Longhua District Central Hospital, Shenzhen, Guang Dong, P.R. China.
Rationale:
Dilated cardiomyopathy (DCM) is a major cause of chronic heart failure, and some patients continue to deteriorate despite guideline-directed medical therapy. Immunoadsorption (IA), which removes pathogenic autoantibodies, has been proposed as a potential adjunctive therapy, but its clinical use remains limited. This case illustrates the potential benefits of IA in advanced, treatment-refractory DCM.
Patient Concerns:
A 53-year-old woman with a 9-year history of DCM presented with recurrent chest tightness and dyspnea. Despite long-term guideline-directed medical therapy, her symptoms progressively worsened.
Diagnoses:
The patient had chronic DCM initially diagnosed in the peripartum period, with a left ventricular ejection fraction (LVEF) of 11% at onset. Before IA, echocardiography demonstrated severe systolic dysfunction (LVEF 22%-24%) with significant mitral regurgitation, and laboratory evaluation showed markedly elevated pro-BNP (4454 pg/mL).
Interventions:
The patient underwent two sessions of immunoadsorption in September 2024, followed by high-dose intravenous immunoglobulin (IVIG) as per standard protocols.
Outcomes:
Following treatment, her symptoms improved, pro-BNP decreased to 2109 pg/mL, and repeat echocardiography showed an increase in LVEF to 29.2%.
Lessons:
This case suggests that immunoadsorption may offer clinical benefit in patients with advanced, refractory DCM. While promising, IA remains experimental and requires further investigation in larger, controlled studies.
関連する概念動画
Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy V: Interprofessional Care
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy IV: Restrictive Cardiomyopathy
Myocarditis III: Medical Management
Heart Failure Drugs: Inotropic Agents

