Galvao-Castro B, Hochmann A, Lambert P H
Clin Exp Immunol. 1978 Jul;33(1):12-24.
A variety of tissue lesions occurs in African trypanosomiasis, in the pathogenesis of which direct toxic effects of the parasite as well as immunological mechanisms may be involved. The purpose of the present study was to evaluate the role of the host immune response in inducing tissue damage in this disease and particularly in the production of lesions in striated muscle. The development of muscle lesions in T. brucei infection was studied in several groups of mice with different forms of immunodeficiency, as well as in normal mice. In the normal mice, foci of intense inflammation and necrosis were found in the cardiac and skeletal muscles 2 weeks or more after infection. In these lesions, there was a heavy deposition of IgG and IgM, and of trypanosomal antigens. In irradiated, newborn mice, and athymic nude mice infected with T. brucei, these inflammatory lesions were not found, although large numbers of trypanosomes were present between the muscle fibres. The characteristic lesions could be induced in athymic nude mice by transfer of normal spleen cells or of normal T lymphocytes 1 week after the onset of infection. The lesions were also partly induced by transfer of antibody to T. brucei. No antibodies to tissue components, particularly to cardiac myofibrils, were found in any of the infected mice. The results of this study show that immunodeficiency suppresses the development of the characteristic muscle lesions of African trypanosomiasis. The relative importance of humoral and cellular immune mechanisms in the pathogenesis of these lesions is not year clear.
非洲锥虫病会出现多种组织病变,其发病机制可能涉及寄生虫的直接毒性作用以及免疫机制。本研究的目的是评估宿主免疫反应在该疾病诱导组织损伤中的作用,特别是在横纹肌病变形成中的作用。在几组具有不同形式免疫缺陷的小鼠以及正常小鼠中,研究了布氏锥虫感染时肌肉病变的发展情况。在正常小鼠中,感染后2周或更长时间,在心肌和骨骼肌中发现了强烈炎症和坏死灶。在这些病变中,有大量IgG、IgM以及锥虫抗原沉积。在受辐射的新生小鼠和感染布氏锥虫的无胸腺裸鼠中,尽管肌纤维间存在大量锥虫,但未发现这些炎症病变。在感染开始1周后,通过转移正常脾细胞或正常T淋巴细胞,可在无胸腺裸鼠中诱导出特征性病变。将抗布氏锥虫抗体转移也可部分诱导出病变。在任何感染小鼠中均未发现针对组织成分,特别是心肌肌原纤维的抗体。本研究结果表明,免疫缺陷会抑制非洲锥虫病特征性肌肉病变的发展。体液免疫和细胞免疫机制在这些病变发病机制中的相对重要性尚不清楚。