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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...

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Detalles Bibliográficos
Autores principales: Tölle, Markus, Freitag, Helma, Antelmann, Michaela, Hartwig, Jelka, Schuchardt, Mirjam, van der Giet, Markus, Eckardt, Kai-Uwe, Grabowski, Patricia, Scheibenbogen, Carmen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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
Descripción
Sumario:(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.