Vaidya S, Wang C C, Gugliuzza C, Fish J C
Department of Pathology, University of Texas Medical Branch, Galveston, USA.
Clin Transplant. 1998 Oct;12(5):439-44.
Antiphospholipid antibody syndrome (APAS) is a condition associated with recurrent arterial and venous thrombosis, recurrent abortions, and thrombocytopenia either with or without lupus. In this study we have evaluated the impact of APAS on the renal transplant outcome of 174 patients.
Patients' APAS status was determined by the presence of anticardiolipin antibodies (ACA) and a history of clotting disorders. Serum samples from each patient were tested for the presence of ACA by the ELISA method. Transplant outcomes were monitored for > or = 1 yr.
Of 174 patients, 78 received renal transplants. Six of these 78 patients had APAS as evidenced by either recurrent microrenal angiopathy (2 patients), thrombocytopenia (1 patient) or frequent A-V shunt thrombosis (3 patients) along with high titers of ACA of IgM, IgG, or both subtypes at the time of their transplants. Each of these 6 patients thrombosed their renal allografts within a week of their transplants. The other 72 transplanted patients with no APAS were all doing well 1 yr post-transplant. The association between APAS and post-transplant renal thrombosis among these patients is highly significant (p < 0.0001). In contrast, no association was discerned between post-transplant thrombosis and prior sensitization to HLA CONCLUSION: Our data demonstrates that patients with APAS are at high risk for development of post-transplant renal thrombosis.
抗磷脂抗体综合征(APAS)是一种与复发性动静脉血栓形成、复发性流产以及血小板减少症相关的疾病,可伴有或不伴有狼疮。在本研究中,我们评估了APAS对174例患者肾移植结果的影响。
通过抗心磷脂抗体(ACA)的存在以及凝血障碍病史来确定患者的APAS状态。采用酶联免疫吸附测定(ELISA)法检测每位患者血清样本中ACA的存在情况。对移植结果进行了≥1年的监测。
174例患者中,78例接受了肾移植。这78例患者中有6例患有APAS,表现为复发性微小肾血管病变(2例)、血小板减少症(1例)或频繁的动静脉分流血栓形成(3例),并且在移植时伴有高滴度的IgM、IgG或两种亚型的ACA。这6例患者在移植后一周内均发生了肾移植血管血栓形成。其他72例无APAS的移植患者在移植后1年情况均良好。这些患者中APAS与移植后肾血栓形成之间的关联非常显著(p < 0.0001)。相比之下,未发现移植后血栓形成与既往对人类白细胞抗原(HLA)致敏之间存在关联。
我们的数据表明,患有APAS的患者发生移植后肾血栓形成的风险很高。