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系统性红斑狼疮患者辅助性T淋巴细胞细胞表面OKT4抗原表达缺陷。

Defective expression of OKT4 antigen on the cell surface of helper T lymphocytes in a patient with systemic lupus erythematosus.

作者信息

Ichikawa Y, Lavastida M T, Gonzales E B, Daniels J C

出版信息

Clin Exp Rheumatol. 1983 Oct-Dec;1(4):299-305.

PMID:6241856
Abstract

OKT-monoclonal antibodies directed to total T-cells (OKT3), inducer/helper (OKT4) or suppressor/cytotoxic (OKT8) T-cells recognize developmental antigens on human T-cells. We report here an 18 year old male patient with systemic lupus erythematosus who had a prominent decrease in the proportion of OKT4-reactive T-cells in his peripheral blood, although the proportion of OKT3- and OKT8-reactive T-cells were essentially normal. His peripheral blood lymphocytes (PBL) responded well to stimulation by phytohemagglutinin-P (PHA) or concanavalin-A (Con A), which are stimulators for OKT4-reactive T-cells or for both subsets. Furthermore, helper T-cell function for B-cell proliferation was demonstrable in the patient's T-cells which lacked both OKT4 and OKT8 antigens. Trypsinization of PBL from healthy individuals abrogated detection of the OKT4 antigen, and a complete recovery of the antigen was observed after 6 days of culture of the treated PBL. The OKT4 antigen, however, could not be expressed on the patient's PBL after this treatment and incubation. In addition, the patient's serum could not block the recovery of OKT4 antigen on trypsinized T-cells from healthy individuals. The decrease in the percentage of OKT4-reactive T-cells was relatively stable in the patient, while his clinical disease activity and medications were variable. Taken together, these results suggest a defective expression of OKT4 antigen on the helper T-cell subset in this patient.

摘要

针对总T细胞(OKT3)、诱导/辅助性(OKT4)或抑制/细胞毒性(OKT8)T细胞的OKT单克隆抗体可识别人类T细胞上的发育抗原。我们在此报告一名18岁的系统性红斑狼疮男性患者,其外周血中OKT4反应性T细胞比例显著下降,而OKT3和OKT8反应性T细胞比例基本正常。他的外周血淋巴细胞(PBL)对植物血凝素-P(PHA)或刀豆蛋白A(Con A)刺激反应良好,PHA或Con A是OKT4反应性T细胞或两个亚群的刺激物。此外,在该患者缺乏OKT4和OKT8抗原的T细胞中,可证明存在辅助性T细胞对B细胞增殖的功能。来自健康个体的PBL经胰蛋白酶处理后,OKT4抗原检测消失,处理后的PBL培养6天后观察到抗原完全恢复。然而,经此处理和孵育后,该患者的PBL上无法表达OKT4抗原。此外,该患者的血清不能阻断健康个体胰蛋白酶处理的T细胞上OKT4抗原的恢复。该患者OKT4反应性T细胞百分比的下降相对稳定,而其临床疾病活动度和用药情况则有所不同。综上所述,这些结果提示该患者辅助性T细胞亚群上OKT4抗原表达存在缺陷。

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