Jungi T W, McGregor D D
Infect Immun. 1978 Feb;19(2):553-61. doi: 10.1128/iai.19.2.553-561.1978.
Peptone-induced macrophages obtained from gnotobiotic (GB) rats responded poorly to chemotactic stimuli that have a powerful, attractive influence upon the cells of conventional donors. Monocyte recruitment from the circulation into peptone-induced exudates also was impaired in GB subjects. Although relatively more resident cells are present in exudates borne by GB donors, their number cannot in itself account for the sluggish response of peptone-induced cells from GB rats. Neutrophil accumulation in the inflamed peritoneal cavities and their responsiveness in vitro were similar in GB and conventional rats. The levels of serum-derived chemotactic factors were similar in such animals. Furthermore, germ-free rats exhibited no obvious defects in their capacity to generate lymphocyte-dependent monocyte chemotactic activity in situ upon specific stimulation with Listeria monocytogenes. It is suggested that the diminished chemotactic responsiveness of exudate macrophages is related in some way to the level of cell activation. This state of affairs might account for the impairment of delayed-type hypersensitivity in GB animals and their inability to resist intracellular bacterial infections.
从悉生(GB)大鼠获得的蛋白胨诱导的巨噬细胞对趋化刺激反应不佳,而这些趋化刺激对常规供体的细胞有强大的吸引作用。在GB实验对象中,单核细胞从循环系统募集到蛋白胨诱导的渗出液中的过程也受到损害。尽管GB供体产生的渗出液中相对存在更多的驻留细胞,但它们的数量本身并不能解释GB大鼠中蛋白胨诱导细胞的迟缓反应。GB大鼠和常规大鼠炎症腹膜腔中的中性粒细胞积聚及其体外反应性相似。此类动物血清来源的趋化因子水平相似。此外,无菌大鼠在用单核细胞增生李斯特菌进行特异性刺激后,在原位产生淋巴细胞依赖性单核细胞趋化活性的能力方面没有明显缺陷。有人认为,渗出液巨噬细胞趋化反应性降低在某种程度上与细胞活化水平有关。这种情况可能解释了GB动物迟发型超敏反应的损害及其抵抗细胞内细菌感染的无能。