Antigen-specific Immunoadsorption of Anti-acetylcholine Receptor Antibodies from Sera of Patients with Myastenia Gravis

Antigen-specific Immunoadsorption of Anti-acetylcholine Receptor Antibodies from Sera of Patients with Myastenia Gravis
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重症肌无力患者血清抗乙酰胆碱受体抗体的抗原特异性免疫吸附

DOI:
10.3109/10731191003634778
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发表时间:
2010-04-01
期刊:
ARTIFICIAL CELLS BLOOD SUBSTITUTES AND BIOTECHNOLOGY
影响因子:
--
通讯作者:
Li, Fangfang
Li, Fangfang
中科院分区:
其他
文献类型:
--
作者:
Sun, Changyuan;Meng, Fanping;Li, Fangfang

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背景资料:抗乙酰胆碱受体抗体(AChRAb)与神经肌肉接头处AChR α亚基的主要免疫原性区域(MIR)结合是重症肌无力(MG)的主要发病机制。研究方法:将人乙酰胆碱受体(AChR)MIR区的10个氨基酸合成肽段与纤维素微球偶联,制成抗原特异性免疫吸附剂(hMIR 10-CB)。结果如下:hMIR 10-CB可以去除MG血清中的AChRAb 40.3 +/-2.3%,而色氨酸非特异性吸附剂Trp-CB仅为22.4 +/- 1.5%,如在ELISA中测定的,并且还显示出对血细胞、血浆离子和血浆蛋白的良好血液相容性,如在兔全血灌注中检查的。结论:抗原特异性免疫吸附剂hMIR 10-CB可作为MG免疫吸附治疗的候选药物。
Background: The binding of anti-acetylcholine receptor antibodies (AChRAb) to the main immunogenic region (MIR) of AChR alpha-subunit in the neuromuscular junction is the major pathogenesis of myasthenia gravis (MG). Methods: A synthetic peptide of 10 amino acids corresponding to the MIR of human AChR was coupled with cellulose beads to make an antigen-specific immunoadsorbent (hMIR10-CB). Results: The hMIR10-CB could remove AChRAb in MG sera by 40.3 +/- 2.3%, compared to a tryptophan nonspecific adsorbent Trp-CB by only 22.4 +/- 1.5% as determined in ELISA, and also showed good blood compatibility for blood cells, plasma ions and plasma proteins as checked in whole blood perfusion in rabbits. Conclusions: The antigen-specific immunoadsorbent hMIR10-CB can serve as a potential candidate in the immunoadsorption treatment of MG.