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预先形成的免疫复合物所导致的肺和皮肤血管损伤。

Lung and dermal vascular injury produced by preformed immune complexes.

作者信息

Scherzer H, Ward P A

出版信息

Am Rev Respir Dis. 1978 Mar;117(3):551-7. doi: 10.1164/arrd.1978.117.3.551.

Abstract

Tissue injury was studied in rat lung and in the dermal vasculature after the injection of preformed, heterologous immune complexes. In lung, these complexes induced an acute, hemorrhagic alveolitis with large numbers of neutrophils. There were marked increases in permeability and extensive intrapulmonary hemorrhage. Similar changes of lesser magnitude developed at sites of dermal injection of immune complexes. The lung and skin reactions were complement- and neutrophil-dependent. The tissue damage in lung, as measured by permeability changes and development of hemorrhage, appeared to intensify during the first 24 hours and then began to wane. By the second and third day after the acute insult, permeability changes and hemorrhage had returned toward control values. Inflammatory, tissue-damaging reactions did not develop in lung or dermis if heat-aggregated bovine serum albumin was injected in place of immune complexes. This model permits the direct study of lung and vascular injury induced by preformed immune complexes.

摘要

在注射预先形成的异源免疫复合物后,对大鼠肺组织和皮肤血管系统中的组织损伤进行了研究。在肺中,这些复合物引发了急性出血性肺泡炎,伴有大量中性粒细胞。通透性显著增加,肺内广泛出血。在免疫复合物皮肤注射部位也出现了程度较轻的类似变化。肺和皮肤反应依赖补体和中性粒细胞。通过通透性变化和出血情况衡量的肺组织损伤,在最初24小时内似乎加剧,然后开始减弱。在急性损伤后的第二天和第三天,通透性变化和出血已恢复至对照值。如果注射热聚集牛血清白蛋白代替免疫复合物,则肺或真皮中不会发生炎症性组织损伤反应。该模型允许直接研究预先形成的免疫复合物诱导的肺和血管损伤。

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