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外周血淋巴细胞自发产生甲状腺球蛋白自身抗体受T细胞调控,并由可溶性T细胞因子增强。

Spontaneous thyroglobulin autoantibody production by peripheral blood lymphocytes is regulated by T cells and is augmented by soluble T cell factors.

作者信息

Pratt M A, Wall J R

机构信息

Department of Microbiology and Immunology, Queen's University Kingston, Ontario, Canada.

出版信息

Autoimmunity. 1989;3(3):189-99. doi: 10.3109/08916938909099016.

Abstract

In this study we report the spontaneous production of autoimmune anti-thyroglobulin antibodies (Tg Ab) by peripheral blood lymphocytes from patients with autoimmune thyroid disease and the use of these cells to study the regulation of this production in vitro. Using a mitogen free microculture system we have found a significant correlation between an individuals' serum titre and the amount of Tg Ab produced in vitro. At low B:T cell ratios Tg Ab production decreased. Specific depletion of suppressor T cells and helper T cells was accomplished using the monoclonal antibodies OKT 8 and OKT 4 respectively. Suppressor cell depletions resulted in increases in Tg Ab production while depletion of helper cells had no consistent effect. The addition of pokeweed mitogen had no stimulatory effect on spontaneous thyroglobulin antibody production. In contrast, when T cell conditioned media was added to the cells, Tg Ab production increased substantially in all patient cultures tested but not in normal control cultures. The results of this study are consistent with the existence of functional thyroid-antigen specific suppressor cells in the peripheral blood which are actively involved in the regulation of autoantibody producing B cells. The results obtained with the cultures maintained in conditioned media show that autoimmune lymphocytes are extremely sensitive to one or more stimulatory factors present in the media and suggests an important role for the production of soluble lymphocyte factors and the expression of receptors for these factors in the aetiology of autoimmune thyroid disease.

摘要

在本研究中,我们报告了自身免疫性甲状腺疾病患者外周血淋巴细胞自发产生自身免疫性抗甲状腺球蛋白抗体(Tg Ab)的情况,以及利用这些细胞在体外研究该抗体产生的调节机制。通过使用无丝裂原的微培养系统,我们发现个体血清滴度与体外产生的Tg Ab量之间存在显著相关性。在低B:T细胞比例下,Tg Ab的产生减少。分别使用单克隆抗体OKT 8和OKT 4特异性去除抑制性T细胞和辅助性T细胞。去除抑制性细胞导致Tg Ab产生增加,而去除辅助性细胞则没有一致的效果。添加商陆有丝分裂原对自发甲状腺球蛋白抗体的产生没有刺激作用。相反,当将T细胞条件培养基添加到细胞中时,在所有测试的患者培养物中Tg Ab的产生显著增加,但在正常对照培养物中则没有增加。本研究结果与外周血中存在功能性甲状腺抗原特异性抑制性细胞一致,这些细胞积极参与自身抗体产生B细胞的调节。在条件培养基中培养所获得的结果表明,自身免疫性淋巴细胞对培养基中存在的一种或多种刺激因子极为敏感,并提示可溶性淋巴细胞因子的产生及其受体的表达在自身免疫性甲状腺疾病的病因学中起重要作用。

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