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自身免疫性血小板减少性紫癜(ATP)患者的免疫调节缺陷。

Immunoregulatory defect in patients with autoimmune thrombocytopenic purpura (ATP).

作者信息

Peller S, Kaufman S, Shaked U

出版信息

Thymus. 1986;8(6):361-7.

PMID:2949403
Abstract

Con A-induced suppressor cells were studied in 20 patients with autoimmune thrombocytopenic purpura and 20 normal controls. Percentage of suppression was determined on autologous and allogenic lymphocytes during blast transformation with phytohemagglutinin (PHA). In 10 patients and 10 controls helper (T4) and suppressor (T8) subsets were also determined, using monoclonal antibodies. We found a significant decrease in patients' suppressor cell activity both with autologous and allogeneic lymphocytes. Patients' responder lymphocytes were also impaired when tested with normal suppressor cells. The numbers of T4 and T8 in patients was found to be normal although the ratio T4/T8 was somewhat lower than in normal controls. There was a significant direct correlation between the numbers of T4 of patients and their suppressor cell activity on allogeneic lymphocytes suggesting an immunoregulatory defect at the level of induction of suppressor cells.

摘要

对20例自身免疫性血小板减少性紫癜患者和20名正常对照者的刀豆蛋白A诱导抑制细胞进行了研究。在用植物血凝素(PHA)进行母细胞转化期间,测定自体和同种异体淋巴细胞的抑制百分比。在10例患者和10名对照者中,还使用单克隆抗体测定了辅助性(T4)和抑制性(T8)亚群。我们发现,无论是自体淋巴细胞还是同种异体淋巴细胞,患者的抑制细胞活性均显著降低。当用正常抑制细胞进行检测时,患者的反应性淋巴细胞也受损。患者的T4和T8数量正常,尽管T4/T8比值略低于正常对照者。患者的T4数量与其对同种异体淋巴细胞的抑制细胞活性之间存在显著的直接相关性,提示在抑制细胞诱导水平存在免疫调节缺陷。

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