Konishi K, Satoh S, Ida S, Takishima T
Tohoku J Exp Med. 1984 Apr;142(4):381-9. doi: 10.1620/tjem.142.381.
A rabbit model of acute hypersensitivity pneumonitis was produced by immunization and subsequent inhalation of pigeon serum. The pathological features, consisting of alveolitis and interstitial granulomas, were similar to those reported previously in the experimental models. Repeated inhalation challenge of pigeon serum, however, did not develop chronic alveolitis but led to the fading of the disease. It was suggested that desensitization defined as the suppression of delayed hypersensitivity contributed to the mechanism of the fading of the disease. Repeated pigeon serum inhalation without previous immunization by the same antigen could produce a moderate interstitial pneumonitis but did not demonstrate a typical granulomatous histological change in lungs. It was necessary to use adjuvant for producing a complete animal model of hypersensitivity pneumonitis. Antigen-specific antibody response did not directly correlate with the development of the animal model of hypersensitivity pneumonitis.
通过免疫并随后吸入鸽血清建立了急性过敏性肺炎兔模型。其病理特征包括肺泡炎和间质性肉芽肿,与先前在实验模型中报道的相似。然而,重复吸入鸽血清激发并未导致慢性肺泡炎,反而使疾病消退。提示脱敏作用(定义为迟发型超敏反应的抑制)促成了疾病消退机制。在未预先用相同抗原免疫的情况下重复吸入鸽血清可产生中度间质性肺炎,但未显示出肺部典型的肉芽肿组织学变化。使用佐剂对于建立完整的过敏性肺炎动物模型是必要的。抗原特异性抗体反应与过敏性肺炎动物模型的发展没有直接关联。