Votto J J, Barton R W, Gionfriddo M A, Cole S R, McCormick J R, Thrall R S
Sarcoidosis. 1987 Mar;4(1):71-6.
In humans beryllium is known to cause pulmonary granulomata which are histologically indistinguishable from sarcoidosis. There is some evidence in man that beryllium-induced pulmonary granulomata are immunologically mediated. We set out to develop an animal model to study the immunopathogenesis of beryllium-induced granulomatous lung disease. Beryllium sulfate (BeSO4) was injected intratracheally (i.t.) into F344 rats previously immunized to BeSO4. This results in well-formed, sarcoid-like lung granulomata at 6 weeks post BeSO4. There was a conspicuous presence at 4 weeks post BeSO4 of numerous, perivascularly located Langhans' giant cells which preceded the development of well-formed granulomas at 6 weeks. Rats were sacrificed at 4, 6, 8 and 12 weeks after i.t. BeSO4. At the time of sacrifice bronchoalveolar lavage (BAL) was performed; B and T (W3/25+ helper 0X8+ suppressor/cytotoxic) lymphocyte populations were quantitated and compared to lymphocyte populations obtained from lung tissue. Both B and T cells were significantly elevated in lung tissue post BeSO4. At 4 weeks when granulomata were just developing, a W3/25+ to 0X8+ ratio of 20:1 in lavage and 2:1 in lung tissue was seen. At 6 weeks when granulomata were well-formed there was a predominance of W3/25+ cells in lavage but not in lung tissue. At 8 and 12 weeks, when the granulomata were regressing, lavage fluid still contained a W3/25+ predominance in contrast to lung tissue which contained a predominance of 0X8+ cells.(ABSTRACT TRUNCATED AT 250 WORDS)
已知在人类中,铍会引发肺肉芽肿,其组织学特征与结节病无法区分。在人类中有一些证据表明,铍诱导的肺肉芽肿是由免疫介导的。我们着手建立一种动物模型,以研究铍诱导的肉芽肿性肺病的免疫发病机制。将硫酸铍(BeSO4)经气管内(i.t.)注入先前已对BeSO4免疫的F344大鼠体内。在注入BeSO4后6周,这导致形成了形态良好的、类似结节病的肺肉芽肿。在注入BeSO4后4周,明显出现大量位于血管周围的朗汉斯巨细胞,这些巨细胞先于6周时形态良好的肉芽肿形成。在经气管内注入BeSO4后4、6、8和12周处死大鼠。在处死时进行支气管肺泡灌洗(BAL);对B淋巴细胞和T淋巴细胞(W3/25 +辅助性0X8 +抑制性/细胞毒性)群体进行定量,并与从肺组织获得的淋巴细胞群体进行比较。注入BeSO4后,肺组织中的B细胞和T细胞均显著升高。在4周时肉芽肿刚形成,灌洗中W3/25 +与0X8 +的比例为20:1,肺组织中为2:1。在6周时肉芽肿形成良好,灌洗中W3/25 +细胞占优势,但肺组织中并非如此。在8周和12周时,肉芽肿正在消退,与含有大量0X8 +细胞的肺组织形成对比的是,灌洗液中仍以W3/25 +细胞占优势。(摘要截短至250字)