Kubota T, Tanoue K, Murohashi I, Nara N, Yamamoto N, Yamazaki H, Aoki N
First Department of Internal Medicine, Tokyo Medical and Dental University, Japan.
Thromb Res. 1989 Feb 15;53(4):379-86. doi: 10.1016/0049-3848(89)90316-2.
An autoantibody to platelet glycoprotein (GP) II b/III a was produced in a 38 year-old woman who had a previous history of the malignant lymphoma of the stomach. The aggregations of the patient's platelets showed losses of the primary waves in response to ADP and epinephrine and marked hypoaggregation in response to collagen, while agglutination by ristocetin was normal. Crossed immuno-electrophoresis (CIE) of her platelets solubilized by 1% Triton X-100 revealed an abnormal biphasic precipitate line of GP II b/III a complex. Nine months later, she developed severe thrombocytopenia along with a relapse of the lymphoma in the cervical lymph nodes. The patient's IgG, which was collected during her thrombocytopenic period and purified, inhibited ADP-, epinephrine- and collagen-induced aggregations of normal platelets. In CIE, the 125I-labelled IgG of the patient, inserted into the intermediate gel, was incorporated into the precipitation line of the GP II b/III a complex of normal platelets. Radiation treatment to the cervical lymph nodes dramatically normalized both the function and the count of the patient's platelets. From these findings, it is suggested that an autoantibody to the GP II b and/or III a was produced by the lymphoma cells.
一名38岁女性体内产生了血小板糖蛋白(GP)II b/III a自身抗体,该女性曾有胃恶性淋巴瘤病史。患者血小板聚集试验显示,其对ADP和肾上腺素的反应中初级波缺失,对胶原的反应明显低聚集,而对瑞斯托菌素的凝集反应正常。用1% Triton X - 100溶解患者血小板后进行交叉免疫电泳(CIE),结果显示GP II b/III a复合物出现异常的双相沉淀线。九个月后,她出现严重血小板减少症,同时颈部淋巴结淋巴瘤复发。在患者血小板减少期采集并纯化的IgG,可抑制正常血小板由ADP、肾上腺素和胶原诱导的聚集。在CIE中,将患者的125I标记IgG插入中间凝胶,可掺入正常血小板GP II b/III a复合物的沉淀线中。对颈部淋巴结进行放射治疗后,患者血小板的功能和计数显著恢复正常。从这些发现提示,淋巴瘤细胞产生了针对GP II b和/或III a的自身抗体。