Satomi S, Tanimura S, Kunori T, Taguchi Y, Kasai M
Transplantation. 1983 Apr;35(4):324-8. doi: 10.1097/00007890-198304000-00012.
The protein-A plaque assay was used for serial monitoring of spontaneous plaque-forming lymphocytes (PFC) in blood or thoracic duct lymph of 30 renal transplant patients. In patients experiencing early or delayed graft rejection, PFC manifested a 10-fold increase over the preoperative or control level within one month of the transplantation. Patients accepting the renal graft did not exhibit a remarkable PFC response. Among the factors examined (proportion of B cells, donor source, acute tubular necrosis, intraoperative blood transfusion, antilymphocyte serum, histocompatibility, and rejection), the PFC response was most closely related to graft rejection. Changes in serum immunoglobulin (Ig) did not appear to correlate with the PFC response. By using Ig-class-specific antisera, secreted Ig was identified as IgG, IgM, and IgA. This may indicate that renal grafts induce polyclonal activation of the recipient's B cells.
采用蛋白A空斑试验对30例肾移植患者血液或胸导管淋巴液中自发形成空斑的淋巴细胞(PFC)进行连续监测。在发生早期或延迟移植排斥反应的患者中,PFC在移植后1个月内比术前或对照水平增加了10倍。接受肾移植的患者未表现出明显的PFC反应。在所检查的因素(B细胞比例、供体来源、急性肾小管坏死、术中输血、抗淋巴细胞血清、组织相容性和排斥反应)中,PFC反应与移植排斥反应关系最为密切。血清免疫球蛋白(Ig)的变化似乎与PFC反应无关。通过使用Ig类特异性抗血清,分泌的Ig被鉴定为IgG、IgM和IgA。这可能表明肾移植诱导受体B细胞的多克隆激活。