Levin Mariano J, Hoebeke Johan
Laboratorio de Biología Molecular de la Enfermedad de Chagas, Instituto de Investigaciones en Ingeniería Genética y Biología Molecular, Consejo Nacional de Investigación, Ciencia y Tecnica, Buenos Aires, Argentina.
Autoimmunity. 2008 Sep;41(6):429-33. doi: 10.1080/08916930802031702.
Anti-beta(1)-adrenoceptor autoantibodies, first described in sera of patients with Chagas' disease, are now well documented in patients with idiopathic dilated cardiomyopathy. The following review summarizes the knowledge we have about the structural basis of receptor-antibody interactions, about their mechanisms of action and about their pathogenicity. While the origin of anti-receptor antibodies with agonist-like activity in Chagas' disease might be ascribed to recognition by anti-parasite antibodies of an epitope, localized on the second extracellular loop of the beta(1)-adrenoceptor, the origin of such antibodies in idiopathic dilated cardiomyopathy remains unknown. The hypothesis of a similar origin for anti-receptor antibodies in both diseases is forwarded.
抗β(1)-肾上腺素能受体自身抗体最早在恰加斯病患者的血清中被描述,如今在特发性扩张型心肌病患者中也有充分记录。以下综述总结了我们对抗受体抗体相互作用的结构基础、其作用机制及其致病性的认识。虽然在恰加斯病中具有激动剂样活性的抗受体抗体的起源可能归因于抗寄生虫抗体对位于β(1)-肾上腺素能受体第二个细胞外环上的一个表位的识别,但在特发性扩张型心肌病中此类抗体的起源仍不清楚。文中提出了两种疾病中抗受体抗体起源相似的假说。