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T-cell recognition of acetylcholine receptor provides a reliable means for monitoring autoimmunity to acetylcholine receptor in antibody-negative myasthenia gravis patients

机译:T细胞对乙酰胆碱受体的识别为监测抗体阴性重症肌无力患者对乙酰胆碱受体的自身免疫性提供了可靠的手段

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摘要

Myasthenia gravis (MG) is an autoimmune disease usually associated with autoantibodies (auto-Abs) against nicotinic acetylcholine receptor (AChR). Some MG patients appear negative for anti-AChR Abs (seronegative), and a fraction of these have auto-Abs against muscle-specific kinase. The remaining patients, although displaying MG symptoms, show no detectable auto-Abs. We describe here a possible association of a rare human leukocyte antigen (HLA)-DQ type and AChR Ab-negative MG. We also found that the majority of seronegative patients exhibit an anti-AChR autoimmune T lymphocyte response. We investigated the existence of AChR-reactive T cells in peripheral blood lymphocytes from seronegative patients by their proliferative responses against a mixture of 18 overlapping synthetic peptides encompassing the extracellular part of human AChR α-chain. Of the 10 samples, eight exhibited positive T-cell proliferative responses against the peptide mixtures. The proliferative assay was equally efficient using a mixture of eight peptides frequently recognized by MG T cells. This T-cell proliferative assay should provide a reliable method for monitoring seronegative MG patients.
机译:重症肌无力(MG)是一种自身免疫性疾病,通常与针对烟碱乙酰胆碱受体(AChR)的自身抗体(auto-Abs)相关。一些重症肌无力患者出现抗AChR抗体阴性(血清阴性),其中部分患者具有针对肌肉特异性激酶的自身Abs。其余患者尽管表现出MG症状,但未显示出可检测到的自身抗体。我们在这里描述了罕见的人类白细胞抗原(HLA)-DQ类型和AChR Ab阴性MG的可能关联。我们还发现,大多数血清阴性患者均表现出抗AChR自身免疫性T淋巴细胞反应。我们研究了血清反应阴性患者外周血淋巴细胞中AChR反应性T细胞的存在,其反应是针对18种重叠的合成肽混合物的增生反应,这些肽段涵盖人AChRα链的胞外部分。在10个样品中,有8个显示出对肽混合物的阳性T细胞增殖反应。使用经常被MG T细胞识别的八种肽的混合物,增殖试验同样有效。这种T细胞增殖测定法应提供监测MG血清阴性患者的可靠方法。

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