Chusid M J, Bujak J S, Dale D C
Blood. 1975 Dec;46(6):921-30.
Humans and grey collie dogs with cyclic neutropenia are known to suffer from an increased rate of bacterial infection. Because of the previously described microanatomic abnormalities of lysosome formation found in the polymorphonuclear leukocytes (PMNs) of dogs with canine cyclic neutropenia, studies of these cells were undertaken. PMNs from grey collie dogs were found to have significant metabolic and functional abnormalities when compared with normal collie PMNs. These included abnormally increased postphagocytic C1-glucose oxidation, decreased iodination of trichloroacetic acid-precipitable protein in the resting and phagocytizing state, decreased levels of intracellular myeloperoxidase,and a bactericidal defect against a variety of bacteria. Phagocytosis was normal. These abnormalities appear to differ from those previously described in the PMNs of patients with chronic granulomatous disease of childhood and the Chediak-Higashi syndrome and more closely resemble those seen in hereditary myeloperoxidase deficiency. Thus, the studies reported here demonstrate defective PMN function in a disease state previously believed to be a model only of periodic hematopoiesis.
已知患有周期性中性粒细胞减少症的人类和灰色柯利犬易患细菌感染率增加的疾病。由于先前描述的犬类周期性中性粒细胞减少症犬的多形核白细胞(PMN)中溶酶体形成的微观解剖学异常,对这些细胞进行了研究。与正常柯利犬的PMN相比,发现灰色柯利犬的PMN存在明显的代谢和功能异常。这些异常包括吞噬后C1-葡萄糖氧化异常增加、静息和吞噬状态下三氯乙酸可沉淀蛋白的碘化减少、细胞内髓过氧化物酶水平降低以及对多种细菌的杀菌缺陷。吞噬作用正常。这些异常似乎与先前在儿童慢性肉芽肿病和切-东综合征患者的PMN中描述的异常不同,更类似于遗传性髓过氧化物酶缺乏症中所见的异常。因此,此处报道的研究表明,在一种先前被认为仅是周期性造血模型的疾病状态下,PMN功能存在缺陷。