Mullins R J, Cohen S B, Webb L M, Chernajovsky Y, Dayan C M, Londei M, Feldmann M
Mathilda and Terence Kennedy Institute of Rheumatology, Hammersmith, London, United Kingdom.
J Clin Invest. 1995 Jul;96(1):30-7. doi: 10.1172/JCI118034.
The importance of thyrotropin receptor (TSHR) agonist antibodies in the manifestations of Graves' disease (GD) is recognized. There are, however, no convincing reports of TSHR-specific T cells. We have previously cloned T cells specific for thyroglobulin and thyroid peroxidase (TPO) from GD lymphoid infiltrates and used autologous EBV-transformed B cell lines (EBVL) transfected with an expression vector encoding TPO to efficiently detect TPO-specific T cells. Here we used EBVL transfected with TSHR to seek TSHR-specific T cells in the GD infiltrates, after cloning the in vivo activated T cells without antigen. 3 out of 30 clones responded vigorously and reproducibly to EBVL-TSHR, with a mean stimulation index > 7. Their release of IL-2, IL-4, and IL-10 after stimulation with soluble anti-CD3 and phorbol ester was indistinguishable from the other clones from this thyroid. However, they produced relatively little IFN gamma (median IL-4/IFN gamma ratio of 0.80) compared with the other clones (median IL-4/IFN gamma ratio 0.06). Thus, this new potent method of antigen presentation, using autoantigen-transfected EBVL, has permitted the first unequivocal identification of TSHR T cells in GD thyroid, with distinct Th0/Th2 characteristics, unlike previously cloned TPO-responsive cells which have Th1 characteristics.
促甲状腺激素受体(TSHR)激动剂抗体在格雷夫斯病(GD)临床表现中的重要性已得到认可。然而,尚无关于TSHR特异性T细胞的确凿报道。我们之前已从GD淋巴浸润物中克隆出甲状腺球蛋白和甲状腺过氧化物酶(TPO)特异性T细胞,并使用用编码TPO的表达载体转染的自体EB病毒转化B细胞系(EBVL)来有效检测TPO特异性T细胞。在此,我们在克隆体内无抗原激活的T细胞后,使用转染了TSHR的EBVL在GD浸润物中寻找TSHR特异性T细胞。30个克隆中有3个对EBVL-TSHR有强烈且可重复的反应,平均刺激指数>7。在用可溶性抗CD3和佛波酯刺激后,它们释放的白细胞介素-2(IL-2)、白细胞介素-4(IL-4)和白细胞介素-10与来自该甲状腺的其他克隆没有区别。然而,与其他克隆相比(IL-4/干扰素γ中位数比值为0.06),它们产生的干扰素γ相对较少(IL-4/干扰素γ中位数比值为0.80)。因此,这种使用自身抗原转染的EBVL的新的有效抗原呈递方法首次明确鉴定出了GD甲状腺中的TSHR T细胞,其具有独特的Th0/Th2特征,这与之前克隆的具有Th1特征的TPO反应性细胞不同。