Schulz L C, Drommer W, Seidler D, Ehard H, Leimbeck R, Weiss R
Beitr Pathol. 1975;154(1):27-51.
In part I of this paper (Schulz et al., 1975) it was shown that in the initial phase of experimental erysipelas a transition from the vascular processes to a systemic connective tissue reaction can be demonstrated in different species. It is the purpose of this paper to describe the chronic phase of the disease with special emphasis on polyarthritis.
12 spontaneously diseased and 22 experimentally infected pigs were used in experiments to study the pathogenesis of the disease. In addition, 74 Wistar rats and 148 Sprague-Dawley rats were used in the experiments. All experimental animals were specific-pathogen-free and were parenterally infected with the standardized E. insidiosa serotype B strain T 28. The observation period for the pigs was up to 2 years, for the rats up to 11 months. The methods used for pathohistological and electron microscopical studies are described in part I. Immunihistological studies were carried out on synovial tissue with peroxidase-conjugates of goat-anti-pig-IgG, goat-anti-pig-IgM, pig-collagen, E. insidiosa-homogenate and heat-aggregated-pig-IgG. Furthermore, goat-anti-pig-IgG and rabbit-anti-pig-C3 conjugated with FITC were used. Passive hemagglutination tests and Latex agglutination test (Singer and Plotz) were performed to demonstrate rheumatoid factors and collagen antibodies.
Polyarthritis occurred in pigs between the 4th and 10th day p.i. and between the 4th and 8th day p.i. in nearly 100% of the infected rats. Fibrinous exudation, proliferation and destruction with pannus formation are marked in most of the joints examined during the first three months. Fibrosis begins 30 days p.i. in the rats' joints and is most severe in both species between the 5th and 8th month. 3 types of lining cells may be differentiated electron microscopically: A (M) cells, B (F) cells and an intermediate form which is found in both species most frequently. Swelling of the endothelial cells together with constriction of the lumen and thickening of the basal membrane occurs in the capillaries.
A comparison of chronic erysipelas polyarthritis in pigs and rats with rheumatoid arthritis of men reveals many morphological and immunological similarities between the two diseases. Systemic connective tissue activation manifests itself in organs predilected for rheumatic changes, such as heart valves, endocardium and joints. The possible prepetuation of the processes by specific or nonspecific immunomechanisms or by deposits of fibrin is discussed. In addition, experimental erysipelas is reproducible in nearly 100% of the animals given one single subcutaneous application of one defined bacteria strain. Therefore too, erysipelas is suited as an animal model for human rheumatic diseases.
在本文的第一部分(舒尔茨等人,1975年)表明,在实验性丹毒的初始阶段,可以在不同物种中证明从血管过程向全身性结缔组织反应的转变。本文的目的是描述该疾病的慢性期,特别强调多关节炎。
使用12只自发患病和22只实验感染的猪来研究该疾病的发病机制。此外,实验中还使用了74只Wistar大鼠和148只Sprague-Dawley大鼠。所有实验动物均无特定病原体,并经肠胃外途径感染标准化的B型内氏杆菌血清型T 28菌株。猪的观察期长达2年,大鼠的观察期长达11个月。病理组织学和电子显微镜研究方法在第一部分中已有描述。免疫组织学研究是在滑膜组织上进行的,使用了山羊抗猪IgG、山羊抗猪IgM、猪胶原蛋白、内氏杆菌匀浆和热聚集猪IgG的过氧化物酶结合物。此外,还使用了与FITC结合的山羊抗猪IgG和兔抗猪C3。进行了被动血凝试验和乳胶凝集试验(辛格和普洛茨)以检测类风湿因子和胶原抗体。
猪在感染后第4至10天出现多关节炎,几乎100%的感染大鼠在感染后第4至8天出现多关节炎。在最初三个月检查的大多数关节中,有明显的纤维蛋白渗出、增殖和破坏,并伴有血管翳形成。大鼠关节在感染后30天开始纤维化,在第5至8个月时两种动物的纤维化最为严重。电子显微镜下可区分出3种衬里细胞:A(M)细胞、B(F)细胞以及在两种动物中最常见的中间形式。毛细血管中内皮细胞肿胀,管腔狭窄,基底膜增厚。
将猪和大鼠的慢性丹毒多关节炎与人类类风湿关节炎进行比较,发现这两种疾病在形态学和免疫学上有许多相似之处。全身性结缔组织活化在易发生风湿性改变的器官中表现出来,如心脏瓣膜、心内膜和关节。讨论了通过特异性或非特异性免疫机制或纤维蛋白沉积使这些过程持续存在的可能性。此外,在几乎100%单次皮下接种一种特定菌株的动物中可重现实验性丹毒。因此,丹毒也适合作为人类风湿性疾病的动物模型。