Reis D D, Jones E M, Tostes S, Lopes E R, Chapadeiro E, Gazzinelli G, Colley D G, McCurley T L
Departamento de Bioquimica e Imunologia, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Am J Trop Med Hyg. 1993 Aug;49(2):192-200. doi: 10.4269/ajtmh.1993.49.192.
We have previously reported that heart lesions in patients with chronic cardiac Chagas' disease are composed predominantly of granzyme A+, cytolytic CD8+ T lymphocytes. We now pursue this study in the immunopathology of chronic chagasic cardiomyopathy by investigation of the expression of HLA antigens, and adhesion molecules in the hearts of seven chagasic patients with cardiac disease, two asymptomatic chagasic patients, and seven normal controls. Comparative immunohistochemical analyses show that HLA-ABC antigen expression is enhanced on the myocardial cells of chagasic patients with chronic cardiomyopathy, suggesting a possible role for these cells as targets for the CD8+ cytolytic lymphocytes dominant in these lesions. The HLA-DR antigens are not observed on myocardial cells, but are consistently upregulated on the endothelial cells in the hearts of patients with chronic chagasic cardiomyopathy. Intercellular adhesion molecule is expressed by endothelial cells of both chagasic and nonchagasic individuals, but E-selectin was detected only on vessels of hearts from chagasic patients who had chronic cardiomyopathy. Most of the lymphocytes in these lesions express lymphocyte function antigen-1 (LFA-1), CD44, and very late antigen-4, and a few display weak expression of LFA-3. We propose that the expression of these adhesion molecules and major histocompatibility complex antigens by endothelial cells, myocardial cells, and lymphoid cells in these lesions contribute to the pathogenesis of chronic chagasic cardiomyopathy.
我们之前报道过,慢性恰加斯病性心脏病患者的心脏病变主要由颗粒酶A阳性、具有细胞溶解作用的CD8 + T淋巴细胞构成。我们现在通过研究7例恰加斯病性心脏病患者、2例无症状恰加斯病患者以及7例正常对照者心脏中HLA抗原和黏附分子的表达,来继续这项关于慢性恰加斯病性心肌病免疫病理学的研究。比较免疫组织化学分析显示,慢性心肌病恰加斯病患者的心肌细胞上HLA - ABC抗原表达增强,提示这些细胞可能作为这些病变中占主导的CD8 + 细胞溶解淋巴细胞的靶细胞发挥作用。心肌细胞上未观察到HLA - DR抗原,但在慢性恰加斯病性心肌病患者心脏的内皮细胞上持续上调。细胞间黏附分子在恰加斯病患者和非恰加斯病个体的内皮细胞中均有表达,但仅在患有慢性心肌病的恰加斯病患者心脏血管上检测到E - 选择素。这些病变中的大多数淋巴细胞表达淋巴细胞功能抗原 - 1(LFA - 1)、CD44和极晚期抗原 - 4,少数显示LFA - 3的弱表达。我们认为,这些病变中的内皮细胞、心肌细胞和淋巴细胞表达这些黏附分子和主要组织相容性复合体抗原有助于慢性恰加斯病性心肌病的发病机制。