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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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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