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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(2)-adrenoreceptor antibodies (ß(2)AR-AB). In a first proof-of-concept study, we cou...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465279/ https://www.ncbi.nlm.nih.gov/pubmed/32751659 http://dx.doi.org/10.3390/jcm9082443 |
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author | Tölle, Markus Freitag, Helma Antelmann, Michaela Hartwig, Jelka Schuchardt, Mirjam van der Giet, Markus Eckardt, Kai-Uwe Grabowski, Patricia Scheibenbogen, Carmen |
author_facet | Tölle, Markus Freitag, Helma Antelmann, Michaela Hartwig, Jelka Schuchardt, Mirjam van der Giet, Markus Eckardt, Kai-Uwe Grabowski, Patricia Scheibenbogen, Carmen |
author_sort | Tölle, Markus |
collection | PubMed |
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(2)-adrenoreceptor antibodies (ß(2)AR-AB). In a first proof-of-concept study, we could show that IA was effective to reduce ß(2)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(2)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. |
format | Online Article Text |
id | pubmed-7465279 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74652792020-09-04 Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Efficacy of Repeat Immunoadsorption Tölle, Markus Freitag, Helma Antelmann, Michaela Hartwig, Jelka Schuchardt, Mirjam van der Giet, Markus Eckardt, Kai-Uwe Grabowski, Patricia Scheibenbogen, Carmen J Clin Med Article (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(2)-adrenoreceptor antibodies (ß(2)AR-AB). In a first proof-of-concept study, we could show that IA was effective to reduce ß(2)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(2)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. MDPI 2020-07-30 /pmc/articles/PMC7465279/ /pubmed/32751659 http://dx.doi.org/10.3390/jcm9082443 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Tölle, Markus Freitag, Helma Antelmann, Michaela Hartwig, Jelka Schuchardt, Mirjam van der Giet, Markus Eckardt, Kai-Uwe Grabowski, Patricia Scheibenbogen, Carmen Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Efficacy of Repeat Immunoadsorption |
title | 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_short | Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Efficacy of Repeat Immunoadsorption |
title_sort | myalgic encephalomyelitis/chronic fatigue syndrome: efficacy of repeat immunoadsorption |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465279/ https://www.ncbi.nlm.nih.gov/pubmed/32751659 http://dx.doi.org/10.3390/jcm9082443 |
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