Visvanathan S, McNeil H P
Inflammation Research Unit, School of Pathology, University of New South Wales, Sydney, Australia.
J Immunol. 1999 Jun 1;162(11):6919-25.
Patients with antiphospholipid syndrome (APS) suffer recurrent thromboses, thrombocytopenia, and/or fetal loss in association with Abs that can be detected in phospholipid-dependent assays. Despite the name, the Igs associated with APS are predominantly directed against epitopes on phospholipid-binding plasma proteins, such as beta 2-glycoprotein-1 (beta 2GP1) and prothrombin. The aim of this study was to examine the cellular immune response to beta 2GP1 in patients with APS. Using a serum-free stimulation assay, PBMCs from 8 of 18 patients with APS proliferated to purified beta 2GP1 or to the beta 2GP1 present in serum, whereas no stimulation was observed by PBMCs from healthy individuals, patients with other autoimmune diseases, or anticardiolipin Ab-positive patients without histories of thromboses or fetal loss. The immune response was Ag-specific, requiring class II molecules, CD4+ T cells, and APCs, and was associated with a selective expansion of CD4+ but not CD8+ T cells. The proliferating T cells produced IFN-gamma but not IL-4, indicating a bias toward a type 1 immune response. Chronic low grade stimulation of autoreactive beta 2GP1-specific, IFN-gamma-producing Th1 CD4+ T cells may contribute to the high risk of thromboses and pregnancy failure in patients with APS.
抗磷脂综合征(APS)患者会反复出现血栓形成、血小板减少和/或胎儿丢失,这些情况与可在磷脂依赖性检测中检测到的自身抗体相关。尽管有这个名称,但与APS相关的免疫球蛋白主要针对磷脂结合血浆蛋白上的表位,如β2糖蛋白1(β2GP1)和凝血酶原。本研究的目的是检测APS患者对β2GP1的细胞免疫反应。使用无血清刺激试验,18例APS患者中有8例的外周血单个核细胞(PBMC)对纯化的β2GP1或血清中存在的β2GP1发生增殖反应,而健康个体、其他自身免疫性疾病患者或无血栓形成或胎儿丢失病史的抗心磷脂抗体阳性患者的PBMC未观察到刺激反应。该免疫反应具有抗原特异性,需要II类分子、CD4 + T细胞和抗原呈递细胞(APC)参与,并且与CD4 + T细胞而非CD8 + T细胞的选择性扩增相关。增殖的T细胞产生γ干扰素但不产生白细胞介素4,表明偏向1型免疫反应。自身反应性β2GP1特异性、产生γ干扰素的Th1 CD4 + T细胞的慢性低水平刺激可能导致APS患者血栓形成和妊娠失败的高风险。