Alexander E, Buyon J P, Provost T T, Guarnieri T
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Arthritis Rheum. 1992 Feb;35(2):176-89. doi: 10.1002/art.1780350209.
To determine whether anti-Ro/SS-A antibodies selectively bind to neonatal cardiac cells and alter membrane repolarization.
An in vitro electrophysiologic and immunocytochemical experimental model contrasting neonatal and rabbit cardiac tissue was employed.
Sera and IgG-enriched fractions from anti-Ro/SS-A antibody-positive mothers of infants with neonatal lupus erythematosus and congenital heart block bind to neonatal, rather than adult, rabbit cardiac tissue and alter the transmembrane action potential (i.e., inhibit repolarization). The additional presence of anti-La/SS-B antibodies was not additive or synergistic for these immunocytochemical and electrophysiologic features. Sera containing other antibody specificities (i.e., anti-native DNA, cardiolipin, Sm, and nuclear RNP) failed to stain the neonatal cardiac tissue or produced alterations in membrane repolarization.
Anti-Ro/SS-A antibodies may play a pathophysiologic role in the development of congenital heart block in neonatal lupus.
确定抗Ro/SS-A抗体是否选择性地结合新生儿心肌细胞并改变膜复极化。
采用对比新生儿和兔心脏组织的体外电生理和免疫细胞化学实验模型。
来自患有新生儿狼疮和先天性心脏传导阻滞婴儿的抗Ro/SS-A抗体阳性母亲的血清和富含IgG的组分与新生兔而非成年兔心脏组织结合,并改变跨膜动作电位(即抑制复极化)。对于这些免疫细胞化学和电生理特征,抗La/SS-B抗体的额外存在并无相加或协同作用。含有其他抗体特异性(即抗天然DNA、心磷脂、Sm和核RNP)的血清未能使新生儿心脏组织染色或引起膜复极化改变。
抗Ro/SS-A抗体可能在新生儿狼疮先天性心脏传导阻滞的发生中起病理生理作用。