Converse P J, Dannenberg A M, Estep J E, Sugisaki K, Abe Y, Schofield B H, Pitt M L
Department of Environmental Health Sciences, School of Hygiene and Public Health, The Johns Hopkins University, Baltimore, Maryland, USA.
Infect Immun. 1996 Nov;64(11):4776-87. doi: 10.1128/iai.64.11.4776-4787.1996.
Liquefaction of solid caseous tuberculous lesions and the subsequent cavity formation are probably the most dangerous processes in the pathogenesis of human pulmonary tuberculosis. In liquefied caseum, the tubercle bacilli grow extracellularly for the first time since the onset of the disease and can reach such large numbers that mutants with antimicrobial resistance may develop. From a cavity, the bacilli enter the bronchial tree and spread to other parts of the lung and also to other people. Of the commonly used laboratory animals, the rabbit is the only one in which cavitary tuberculosis can be readily produced. This report is the first to describe and analyze the complete course of cavitary tuberculosis, produced by aerosolized virulent bovine-type tubercle bacilli in commercially available New Zealand white rabbits. After the inhalation of 220 to 880 bacillary units, all of the rabbits were overtly well until they were sacrificed at 33 weeks. After the inhalation of 3,900 to 5,800 bacillary units, half of the rabbits died of progressive tuberculosis between 5 and 9 weeks and the other half lived until they were sacrificed at 18 weeks. Pulmonary cavities developed in both low- and high-dose groups, some beginning as early as 6 weeks. Bacilli from primary cavities sometimes caused nearby secondary cavities, but more frequently, they ascended the bronchial escalator, were swallowed, and caused secondary tubercles in the lymphoid tissue of the appendix and ileocecal junction. Histologically, and by culture, the number of bacilli found in the liquefied caseum varied from many to comparatively few. Strong tuberculin reactions at 4 weeks after infection were associated with fewer primary lesions, while strong tuberculin reactions at 33 weeks were associated with more cavitary lesions. In the tuberculous granulation tissue surrounding caseous and liquefied pulmonary foci and cavities, we found many mature epithelioid macrophages that contained high levels of the proteinase cathepsin D. Therefore, cathepsin D probably plays a major role in the liquefaction of solid caseous material and in the subsequent cavity formation.
固态干酪样结核病变的液化以及随后的空洞形成可能是人类肺结核发病机制中最危险的过程。在液化的干酪样物质中,结核杆菌自疾病发作以来首次在细胞外生长,数量可能达到如此之多,以至于可能产生具有抗微生物耐药性的突变体。杆菌从空洞进入支气管树,扩散到肺部的其他部位,也传播给其他人。在常用的实验动物中,兔子是唯一一种能够轻易产生空洞性肺结核的动物。本报告首次描述并分析了由雾化的强毒牛型结核杆菌在市售新西兰白兔中产生的空洞性肺结核的完整病程。吸入220至880个杆菌单位后,所有兔子在33周被处死前表面上都很健康。吸入3900至5800个杆菌单位后,一半兔子在5至9周死于进行性肺结核,另一半存活至18周被处死。低剂量和高剂量组均出现了肺空洞,有些早在6周就开始出现。原发性空洞中的杆菌有时会导致附近的继发性空洞,但更常见的是,它们沿着支气管上行,被吞咽,并在阑尾和回盲部交界处的淋巴组织中引起继发性结核结节。从组织学和培养结果来看,在液化的干酪样物质中发现的杆菌数量从很多到相对较少不等。感染后4周强烈的结核菌素反应与较少的原发性病变相关,而33周时强烈的结核菌素反应与较多的空洞性病变相关。在干酪样和液化的肺病灶及空洞周围的结核性肉芽组织中,我们发现了许多含有高水平蛋白酶组织蛋白酶D的成熟上皮样巨噬细胞。因此,组织蛋白酶D可能在固态干酪样物质的液化以及随后的空洞形成中起主要作用。