Behrens B L, Clark R A, Presley D M, Graves J P, Feldsien D C, Larsen G L
Lab Invest. 1987 Jan;56(1):101-13.
Histopathologic changes during the immediate cutaneous response (ICR) and late cutaneous response (LCR) to antigen challenge in allergic humans include dermal edema in the ICR (15 to 30 minutes) followed by increasing cellular infiltration in the LCR (6 hours and more). No description of the evolving histopathologic changes that occur during an immediate asthmatic response (IAR) followed by a late asthmatic response (LAR) exists in either clinical studies or animal models. We examined cutaneous and pulmonary histopathology at 1/2, 6, 24, and 48 hours as well as 7 days after simultaneous intradermal and aerosol antigen challenge of rabbits immunize with Alternaria tenuis extract. Nonimmunized rabbits challenged with Alternaria tenuis extract and immunized rabbits challenged with normal saline served as controls. Immediate wheal and flare responses followed by a LCR were seen in immunized but not control animals. Pulmonary function tests documented immediate and LAR in immunized but not control animals. Thirty minutes after antigen challenge of sensitized animals (ICR and IAR), both dermal sites and large airway submucosal sites had interstitial edema and vessel dilatation while small airways were essentially normal. At 6 hours after challenge, the dermal and large airway submucosal sites of immune animals (LCR and LAR) demonstrated a moderate mixed leukocyte infiltrate as well as residual edema. Additionally, bronchioles and pulmonary vessel adventitia from these responding animals had an intense and widespread leukocyte infiltration. At 24 and 48 hours, immune challenged animals but not controls had a marked mixed cellular infiltrate near skin vessels and near the bronchioles and pulmonary vessels with little or no residual interstitial edema. At 7 days, three of four animals showed resolution of the inflammation while the fourth showed minimal residual changes. Morphometric analysis of airway inflammation substantiated these qualitative observations and demonstrated that the granulocytes around airways of immune rabbits were a mixture of neutrophils and eosinophils at 6 hours, but were predominantly eosinophils at 48 hours. Immunofluorescent studies of skin and lung tissue did not demonstrate any granular or linear deposition of immunoglobulin or complement at the sites of inflammation, however, fibrin deposition was noted in the skin and lungs of immune rabbits. These observations show that immunized rabbits challenged with antigen develop cutaneous and pulmonary inflammation.(ABSTRACT TRUNCATED AT 400 WORDS)
在过敏性个体中,对抗原激发的即刻皮肤反应(ICR)和迟发性皮肤反应(LCR)期间的组织病理学变化包括ICR(15至30分钟)时的真皮水肿,随后是LCR(6小时及更长时间)时细胞浸润增加。在临床研究或动物模型中,均不存在对即刻哮喘反应(IAR)后接着迟发性哮喘反应(LAR)期间不断演变的组织病理学变化的描述。我们在用细交链孢霉提取物免疫的兔子进行皮内和气溶胶抗原激发后,于1/2、6、24和48小时以及7天后检查了皮肤和肺部组织病理学。用细交链孢霉提取物激发的未免疫兔子和用生理盐水激发的免疫兔子作为对照。在免疫动物而非对照动物中观察到即刻风团和潮红反应,随后出现LCR。肺功能测试记录了免疫动物而非对照动物中的即刻反应和LAR。在致敏动物接受抗原激发30分钟后(ICR和IAR),真皮部位和大气道黏膜下部位均出现间质水肿和血管扩张,而小气道基本正常。激发后6小时,免疫动物的真皮和大气道黏膜下部位(LCR和LAR)显示出中度混合白细胞浸润以及残余水肿。此外,这些有反应动物的细支气管和肺血管外膜有强烈且广泛的白细胞浸润。在24和48小时时,接受免疫激发的动物而非对照动物在皮肤血管附近、细支气管和肺血管附近有明显的混合细胞浸润,几乎没有或没有残余间质水肿。在7天时,四只动物中有三只炎症消退,第四只显示出最小程度的残余变化。气道炎症的形态计量学分析证实了这些定性观察结果,并表明免疫兔子气道周围的粒细胞在6小时时是中性粒细胞和嗜酸性粒细胞的混合物,但在48小时时主要是嗜酸性粒细胞。皮肤和肺组织的免疫荧光研究未在炎症部位显示免疫球蛋白或补体的任何颗粒状或线性沉积,然而,在免疫兔子的皮肤和肺中注意到纤维蛋白沉积。这些观察结果表明,用抗原激发免疫兔子会引发皮肤和肺部炎症。(摘要截短至400字)