Chang J C, Jagirdar J, Lesser M
Am J Pathol. 1986 Oct;125(1):16-27.
Granulomatous inflammation was induced in the lungs of rats for assessment of the suitability of this animal species for long-term study of granuloma development and resolution and for comparison of the histologic changes with the cellular profile in bronchoalveolar lavage (BAL) samples. It was found that after a single intravenous injection of bacillus Calmette-Guérin (BCG) organisms suspended in saline-0.01% Triton, complete Freund's adjuvant (CFA), or BCG suspended in CFA (BCG + CFA), distinct pathologic patterns developed in the lungs during the acute stages. BCG alone caused numerous small epithelioid granulomas associated with interstitial infiltration; CFA alone caused large discrete granulomas with minimal interstitial changes, and BCG + CFA caused large granulomas associated with diffuse interstitial infiltration. Following CFA or BCG + CFA the maximum number and size of granulomas were reached approximately 4 weeks after injection. By 8 weeks collagen was seen in the larger granulomas in sections stained with hematoxylin and eosin from animals given CFA or BCG + CFA. Maximum collagen deposition was seen at 16 weeks. From that point onward the degree of collagen deposition decreased, so that by approximately 42 weeks collagen was no longer seen. At 52 weeks residual granulomatous lesions consisted of a few foci of foamy macrophages surrounded by several layers of lymphocytes or epithelioid cells surrounded by dense layers of lymphocytes. Bronchoalveolar lavage samples revealed that at all time periods the number of leukocytes was increased and that the increase was due primarily to an influx of macrophages and lymphocytes. The increase in number of lymphocytes was so striking that at the peak of granulomatous changes following injection of BCG + CFA up to 50% of the total cells were found to be lymphocytes. The total number of leukocytes in BAL samples and the absolute number of lymphocytes closely paralleled the intensity of histologic changes seen in microscopic sections. It is concluded that the intravenous injection of BCG, CFA, or BCG + CFA in rats causes distinct and profound granulomatous patterns that are associated with increased cellularity in BAL samples. The findings suggest that the rat may be an excellent model for study of the mechanisms of granuloma development and resolution.
在大鼠肺部诱导肉芽肿性炎症,以评估该动物物种是否适合用于肉芽肿形成和消退的长期研究,并将组织学变化与支气管肺泡灌洗(BAL)样本中的细胞特征进行比较。结果发现,在单次静脉注射悬浮于含0.01% Triton的生理盐水、完全弗氏佐剂(CFA)或悬浮于CFA中的卡介苗(BCG + CFA)后,肺部在急性期出现了不同的病理模式。单独注射BCG导致大量小上皮样肉芽肿并伴有间质浸润;单独注射CFA导致大的离散性肉芽肿且间质变化最小,而BCG + CFA导致大的肉芽肿并伴有弥漫性间质浸润。注射CFA或BCG + CFA后,肉芽肿的最大数量和大小在注射后约4周达到。到8周时,在给予CFA或BCG + CFA的动物经苏木精和伊红染色的切片中,较大的肉芽肿中可见胶原。在16周时可见最大程度的胶原沉积。从那时起,胶原沉积程度下降,以至于到大约42周时不再可见胶原。在52周时,残留的肉芽肿性病变由一些泡沫巨噬细胞灶组成,周围有几层淋巴细胞,或由密集淋巴细胞层包围的上皮样细胞。支气管肺泡灌洗样本显示,在所有时间段白细胞数量均增加,且增加主要是由于巨噬细胞和淋巴细胞的流入。淋巴细胞数量的增加非常显著,以至于在注射BCG + CFA后肉芽肿变化的高峰期,发现高达50%的总细胞为淋巴细胞。BAL样本中白细胞的总数和淋巴细胞的绝对数量与显微镜切片中所见组织学变化的强度密切平行。结论是,在大鼠中静脉注射BCG、CFA或BCG + CFA会导致明显且深刻的肉芽肿模式,并与BAL样本中细胞增多相关。这些发现表明,大鼠可能是研究肉芽肿形成和消退机制的极佳模型。