Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Efficacy of Repeat Immunoadsorption

被引:28
作者
Toelle, Markus [1 ,2 ,3 ,4 ]
Freitag, Helma [5 ,6 ,7 ,8 ]
Antelmann, Michaela [5 ,6 ,7 ,8 ]
Hartwig, Jelka [5 ,6 ,7 ,8 ]
Schuchardt, Mirjam [1 ,2 ,3 ,4 ]
van der Giet, Markus [1 ,2 ,3 ,4 ]
Eckardt, Kai-Uwe [1 ,2 ,3 ,4 ]
Grabowski, Patricia [5 ,6 ,7 ,8 ]
Scheibenbogen, Carmen [5 ,6 ,7 ,8 ,9 ]
机构
[1] Charite Univ Med Berlin, Dept Nephrol & Med Intens Care, D-12203 Berlin, Germany
[2] Free Univ Berlin, D-12203 Berlin, Germany
[3] Humboldt Univ, D-12203 Berlin, Germany
[4] Berlin Inst Hlth, D-12203 Berlin, Germany
[5] Charite Univ Med Berlin, Inst Med Immunol, D-13353 Berlin, Germany
[6] Free Univ Berlin, D-13353 Berlin, Germany
[7] Humboldt Univ, D-13353 Berlin, Germany
[8] Berlin Inst Hlth, D-13353 Berlin, Germany
[9] Berlin Brandenburg Ctr Regenerat Therapies BCRT, D-13353 Berlin, Germany
关键词
Myalgic Encephalomyelitis; Chronic Fatigue Syndrome; immunoadsorption; ss(2)adrenoreceptor autoantibody; AUTOANTIBODIES; THERAPY;
D O I
10.3390/jcm9082443
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
(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.
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页码:1 / 13
页数:13
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