Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Efficacy of Repeat Immunoadsorption

(1) Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a complex neuroimmunological disease. There is evidence for an autoimmune mechanism for ME/CFS with an infection-triggered onset and dysfunction of ß<sub>2</sub>-adrenoreceptor antibodies (ß<sub>2</sub>AR-AB)....

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Main Authors: Markus Tölle, Helma Freitag, Michaela Antelmann, Jelka Hartwig, Mirjam Schuchardt, Markus van der Giet, Kai-Uwe Eckardt, Patricia Grabowski, Carmen Scheibenbogen
Format: Article
Language:English
Published: MDPI AG 2020-07-01
Series:Journal of Clinical Medicine
Subjects:
Online Access:https://www.mdpi.com/2077-0383/9/8/2443
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spelling doaj-a94d66e0d64b41ef91872981165f02592020-11-25T03:15:27ZengMDPI AGJournal of Clinical Medicine2077-03832020-07-0192443244310.3390/jcm9082443Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Efficacy of Repeat ImmunoadsorptionMarkus Tölle0Helma Freitag1Michaela Antelmann2Jelka Hartwig3Mirjam Schuchardt4Markus van der Giet5Kai-Uwe Eckardt6Patricia Grabowski7Carmen Scheibenbogen8Department of Nephrology and Medical Intensive Care , Charité—Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt Universität zu Berlin, and Berlin Institute of Health, 12203 Berlin, GermanyInstitute of Medical Immunology, Charité—Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt Universität zu Berlin, and Berlin Institute of Health, 13353 Berlin, GermanyInstitute of Medical Immunology, Charité—Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt Universität zu Berlin, and Berlin Institute of Health, 13353 Berlin, GermanyInstitute of Medical Immunology, Charité—Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt Universität zu Berlin, and Berlin Institute of Health, 13353 Berlin, GermanyDepartment of Nephrology and Medical Intensive Care , Charité—Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt Universität zu Berlin, and Berlin Institute of Health, 12203 Berlin, GermanyDepartment of Nephrology and Medical Intensive Care , Charité—Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt Universität zu Berlin, and Berlin Institute of Health, 12203 Berlin, GermanyDepartment of Nephrology and Medical Intensive Care , Charité—Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt Universität zu Berlin, and Berlin Institute of Health, 12203 Berlin, GermanyInstitute of Medical Immunology, Charité—Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt Universität zu Berlin, and Berlin Institute of Health, 13353 Berlin, GermanyInstitute of Medical Immunology, Charité—Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt Universität zu Berlin, and Berlin Institute of Health, 13353 Berlin, Germany(1) Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a complex neuroimmunological disease. There is evidence for an autoimmune mechanism for ME/CFS with an infection-triggered onset and dysfunction of ß<sub>2</sub>-adrenoreceptor antibodies (ß<sub>2</sub>AR-AB). In a first proof-of-concept study, we could show that IA was effective to reduce ß<sub>2</sub>AR-AB and led to improvement of various symptoms. (2) Five of the ME/CFS patients who had clinical improvement following treatment with a five-day IA were retreated in the current study about two years later with a modified IA protocol. The severity of symptoms was assessed by disease specific scores during a follow-up period of 12 months. The antibodies were determined by ELISA. (3) The modified IA treatment protocol resulted in a remarkable similar clinical response. The treatment was well tolerated and 80–90% decline of total IgG and ß<sub>2</sub>AR-AB was achieved. Four patients showed a rapid improvement in several clinical symptoms during IA therapy, lasting for six to 12 months. One patient had no improvement. (4) We could provide further evidence that IA has clinical efficacy in patients with ME/CFS. Data from our pilot trial warrant further controlled studies in ME/CFS.https://www.mdpi.com/2077-0383/9/8/2443Myalgic Encephalomyelitis/Chronic Fatigue Syndromeimmunoadsorptionß2 adrenoreceptor autoantibody
collection DOAJ
language English
format Article
sources DOAJ
author Markus Tölle
Helma Freitag
Michaela Antelmann
Jelka Hartwig
Mirjam Schuchardt
Markus van der Giet
Kai-Uwe Eckardt
Patricia Grabowski
Carmen Scheibenbogen
spellingShingle Markus Tölle
Helma Freitag
Michaela Antelmann
Jelka Hartwig
Mirjam Schuchardt
Markus van der Giet
Kai-Uwe Eckardt
Patricia Grabowski
Carmen Scheibenbogen
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Efficacy of Repeat Immunoadsorption
Journal of Clinical Medicine
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome
immunoadsorption
ß2 adrenoreceptor autoantibody
author_facet Markus Tölle
Helma Freitag
Michaela Antelmann
Jelka Hartwig
Mirjam Schuchardt
Markus van der Giet
Kai-Uwe Eckardt
Patricia Grabowski
Carmen Scheibenbogen
author_sort Markus Tölle
title Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Efficacy of Repeat Immunoadsorption
title_short Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Efficacy of Repeat Immunoadsorption
title_full Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Efficacy of Repeat Immunoadsorption
title_fullStr Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Efficacy of Repeat Immunoadsorption
title_full_unstemmed Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Efficacy of Repeat Immunoadsorption
title_sort myalgic encephalomyelitis/chronic fatigue syndrome: efficacy of repeat immunoadsorption
publisher MDPI AG
series Journal of Clinical Medicine
issn 2077-0383
publishDate 2020-07-01
description (1) Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a complex neuroimmunological disease. There is evidence for an autoimmune mechanism for ME/CFS with an infection-triggered onset and dysfunction of ß<sub>2</sub>-adrenoreceptor antibodies (ß<sub>2</sub>AR-AB). In a first proof-of-concept study, we could show that IA was effective to reduce ß<sub>2</sub>AR-AB and led to improvement of various symptoms. (2) Five of the ME/CFS patients who had clinical improvement following treatment with a five-day IA were retreated in the current study about two years later with a modified IA protocol. The severity of symptoms was assessed by disease specific scores during a follow-up period of 12 months. The antibodies were determined by ELISA. (3) The modified IA treatment protocol resulted in a remarkable similar clinical response. The treatment was well tolerated and 80–90% decline of total IgG and ß<sub>2</sub>AR-AB was achieved. Four patients showed a rapid improvement in several clinical symptoms during IA therapy, lasting for six to 12 months. One patient had no improvement. (4) We could provide further evidence that IA has clinical efficacy in patients with ME/CFS. Data from our pilot trial warrant further controlled studies in ME/CFS.
topic Myalgic Encephalomyelitis/Chronic Fatigue Syndrome
immunoadsorption
ß2 adrenoreceptor autoantibody
url https://www.mdpi.com/2077-0383/9/8/2443
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