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恰加斯病中针对人类心脏传导系统的自身抗体。

Autoantibodies to human heart conduction system in Chagas' disease.

作者信息

Arce-Fonseca Minerva, Ballinas-Verdugo Martha A, Reyes Pedro A, Aranda-Fraustro Alberto, Monteón Victor M

机构信息

Laboratorio de Inmunoparasitología, Instituto Nacional de Cardiología, Ignacio Chávez, México, México.

出版信息

Vector Borne Zoonotic Dis. 2005 Fall;5(3):233-6. doi: 10.1089/vbz.2005.5.233.

Abstract

Destruction of heart tissue in chronic chagasic cardiopathy may be caused by autoimmune recognition of heart tissue. Indirect evidence suggests that there is antigenic cross-reactivity between Trypanosoma cruzi and heart tissue. The objective of this study was to determine whether seric autoantibodies against atrio-ventricular (AV) node and sinus auricular node tissues are markers of chronic cardiopathy condition. We searched for the presence of seric autoantibodies against AV node and sinus auricular node tissues in 25 sera from chronic chagasic cardiopathy patients, 20 sera from non-chagasic cardiopathy patients, 20 sera from indeterminate chagasic subjects, and 20 sera from healthy blood donors as controls. Diagnosis of dilated cardiopathy was established based on the left-ventricular end systolic dimension and cardiothoracic ratio on chest x-radiography and impaired contracting ventricle, and chagasic etiology by demonstration of circulating antibodies using ELISA and IIF. Autoantibody detection against conduction heart tissue was carried out by immunohistochemical test. The tissues were obtained from non-cardiopathy necropsy case. Human sera were diluted at 1:10 in PBS-FSB. Goat antihuman laminin was used as positive control. Autoantibodies were more frequently found in chronic chagasic cardiopathy (20%) compared to non-chagasic cardiopathy (5%) and indeterminate chagasic subjects (5%), pattern staining define interstitial and membrane targets on rich conduction system tissue. In conclusion seric autoantibodies against heart conduction system are not a good markers for chagasic cardiopathy group. Their presence showed no clear association with complex rhythm/conduction aberrations.

摘要

慢性恰加斯病性心肌病中心脏组织的破坏可能是由心脏组织的自身免疫识别引起的。间接证据表明,克氏锥虫与心脏组织之间存在抗原交叉反应。本研究的目的是确定针对房室(AV)结和窦房结组织的血清自身抗体是否为慢性疾病状态的标志物。我们在25例慢性恰加斯病性心肌病患者的血清、20例非恰加斯病性心肌病患者的血清、20例无症状恰加斯病患者的血清以及20例作为对照的健康献血者的血清中,寻找针对AV结和窦房结组织的血清自身抗体。基于胸部X线摄影的左心室收缩末期内径和心胸比以及收缩性心室受损情况,确立扩张型心肌病的诊断,并通过酶联免疫吸附测定(ELISA)和间接免疫荧光法(IIF)检测循环抗体来确定恰加斯病病因。通过免疫组织化学试验检测针对心脏传导组织的自身抗体。这些组织取自非心脏病尸检病例。人血清在PBS - FSB中按1:10稀释。山羊抗人层粘连蛋白用作阳性对照。与非恰加斯病性心肌病(5%)和无症状恰加斯病患者(5%)相比,慢性恰加斯病性心肌病患者中自身抗体的检出率更高(20%),染色模式确定了富含传导系统组织中的间质和膜靶点。总之,针对心脏传导系统的血清自身抗体不是恰加斯病性心肌病组的良好标志物。它们的存在与复杂的节律/传导异常无明显关联。

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