Horsfall A C, Rose L M
Kennedy Institute of Rheumatology, Bute Gardens, London, UK.
J Autoimmun. 1992 Aug;5(4):479-93. doi: 10.1016/0896-8411(92)90007-d.
Epitopes with linear sequences recognized by anti-La autoantibodies from seven mothers of children with congenital heart block were recently defined. Eight of these epitopes share sequence identity with three other proteins in addition to the original autoantigen, La. The three proteins are human cardiac myosin beta heavy chain, laminin B1 chain and the M6 protein of Streptococcus pyogenes. Affinity purified anti-La antibodies from a further three mothers bound to the La antigen and also to human cardiac myosin and mouse laminin. Affinity purified antibodies from three mothers of healthy children bound to the La antigen but showed minimal binding to either human cardiac myosin or mouse laminin. Cardiac myosin inhibited the binding of CHB-related anti-La antibodies to both La and myosin. These data support a role for maternal autoantibodies crossing the placenta and recognizing foetal cardiac antigens accessible at a critical developmental stage during gestation. We suggest that this would lead to complement fixation, inflammation and the subsequent pathology associated with congenital heart block.
最近确定了来自七名先天性心脏传导阻滞患儿母亲的抗La自身抗体所识别的具有线性序列的表位。这些表位中的八个除了与原始自身抗原La外,还与其他三种蛋白质具有序列同一性。这三种蛋白质是人心脏肌球蛋白β重链、层粘连蛋白B1链和化脓性链球菌的M6蛋白。另外三名母亲的亲和纯化抗La抗体与La抗原结合,也与人心脏肌球蛋白和小鼠层粘连蛋白结合。来自三名健康儿童母亲的亲和纯化抗体与La抗原结合,但与人心脏肌球蛋白或小鼠层粘连蛋白的结合最少。心脏肌球蛋白抑制与先天性心脏传导阻滞相关的抗La抗体与La和肌球蛋白的结合。这些数据支持母体自身抗体穿过胎盘并识别妊娠关键发育阶段可及的胎儿心脏抗原的作用。我们认为这将导致补体固定、炎症以及随后与先天性心脏传导阻滞相关的病理变化。