Department of Periodontics, Virginia Commonwealth University School of Dentistry, Richmond, VA, USA.
J Dent Res. 2020 Jul;99(7):797-803. doi: 10.1177/0022034520913244. Epub 2020 Mar 23.
Anticardiolipin antibodies, found at elevated serum concentrations in 15% to 20% of individuals with periodontitis, are associated with adverse pregnancy outcomes, thrombotic conditions, and accelerated atherosclerosis in autoimmune disease such as the antiphospholipid syndrome. Our previous studies demonstrated that antibodies raised in mice against caused fetal loss in a mouse pregnancy model due to anticardiolipin antibodies. Such antibodies are induced via molecular mimicry with the serum protein β2-glycoprotein 1 (β2GP1), the target antigen of anticardiolipin. Furthermore, human anticardiolipin IgG is associated with increased serum markers of vascular inflammation, and IgG purified from periodontitis subjects with elevated anticardiolipin stimulates inflammatory cytokine production by endothelial cells and a trophoblastic cell line. Activation of the trophoblastic cells by anticardiolipin occurs through Toll-like receptor 4. In the present study, we observed that IgG anticardiolipin from periodontitis subjects also causes fetal loss in mice. Displacement of the protective 2-dimensional lattice formed by annexin V on trophoblast surfaces by anticardiolipin, via its interaction with its target antigen β2GP1, leading to fibrin clot formation due to exposure of anionic phospholipids to plasma, is a plausible pathogenic mechanism explaining adverse obstetrical outcomes in antiphospholipid syndrome. Therefore, we assessed such interactions in periodontitis. We observed that anticardiolipin from periodontitis subjects competes for annexin V on an artificial phosphatidylserine monolayer, replicating a key activity of autoantibodies found in patients with antiphospholipid syndrome. In addition, we found that anticardiolipin from periodontitis subjects increases annexin V levels on the BeWo choriocarcinoma cell line, consistent with mobilization of annexin V to the cell surface to facilitate repair following membrane damage. The data indicate that sera and IgG from periodontitis subjects with elevated anticardiolipin levels may influence pregnancy outcomes due to interactions with annexin V.
抗心磷脂抗体在 15%至 20%的牙周炎患者血清中浓度升高,与不良妊娠结局、血栓形成和自身免疫性疾病(如抗磷脂综合征)中的动脉粥样硬化加速有关。我们之前的研究表明,在小鼠中针对 产生的抗体导致小鼠妊娠模型中的胎儿丢失,原因是抗心磷脂抗体。这些抗体是通过与血清蛋白 β2-糖蛋白 1(β2GP1)的分子模拟诱导产生的,β2GP1 是抗心磷脂的靶抗原。此外,人类抗心磷脂 IgG 与血管炎症的血清标志物增加有关,并且从抗心磷脂升高的牙周炎患者中纯化的 IgG 可刺激内皮细胞和滋养层细胞系产生炎症细胞因子。抗心磷脂通过 Toll 样受体 4 激活滋养层细胞。在本研究中,我们观察到牙周炎患者的 IgG 抗心磷脂也可导致小鼠胎儿丢失。抗心磷脂通过与其靶抗原 β2GP1 相互作用,取代 annexin V 在滋养层表面形成的保护性二维晶格,导致由于阴离子磷脂暴露于血浆而形成纤维蛋白凝块,这是一种合理的致病机制,可解释抗磷脂综合征中的不良产科结局。因此,我们评估了牙周炎中的这种相互作用。我们观察到,牙周炎患者的抗心磷脂与人工磷脂酰丝氨酸单层上的 annexin V 竞争,复制了抗磷脂综合征患者自身抗体的关键活性。此外,我们发现,牙周炎患者的抗心磷脂增加了 BeWo 绒毛癌细胞系上 annexin V 的水平,与 annexin V 向细胞表面募集以促进膜损伤后的修复一致。数据表明,由于与 annexin V 的相互作用,血清和 IgG 可能会影响牙周炎患者的妊娠结局。