Laboratory for Leukocyte Functions, Meir Medical Center, Kfar Saba, Israel.
J Clin Immunol. 2012 Jun;32(3):454-66. doi: 10.1007/s10875-011-9633-4. Epub 2011 Dec 30.
There is a paucity of data on the relationship between demographic characteristics, specific clinical manifestations, and neutrophil dysfunction, guiding physicians to decide which clinical signs and symptoms are a code for an underlying phagocytic disorder.
The data over a 21-year period of all adult and pediatric patients referred to our Laboratory for Leukocyte Functions with recurrent pyogenic infections were analyzed. Neutrophil function studies included chemotaxis, superoxide production (SOP), bactericidal activity (BA), and specific studies in case of suspected primary phagocytic disorder (PPD).
Neutrophil dysfunction was found in 33.6% of 998 patients; chemotaxis in 16.6%, SOP in 6%, and BA in 24.5%. The younger the patient and the more organ systems involved, the greater the probability of finding phagocytic impairment. Impaired chemotaxis correlated with recurrent aphthous stomatitis, infections associated with elevated IgE, and purulent upper respiratory tract infections. Impaired SOP and BA correlated with deep-seated abscesses, recurrent lymphadenitis, sepsis, and bone and joint and central nervous system infections. PPDs were identified in 5.7%, chronic granulomatous disease in 4.8%, neutrophil glucose-6-phosphate dehydrogenase deficiency in 0.3%, leukocyte adhesion deficiency type 1 in 0.4%, and myeloperoxidase deficiency in 0.2%. Phagocytic evaluation contributed to the diagnosis of hyperimmunoglobulin-E syndrome (n = 21) and Chediak-Higashi syndrome (n = 3).
PPDs are identified in 5.7% of patients with recurrent pyogenic infections; in the remainder, phagocytic dysfunction may be related to deleterious effects of persistent infection, drug consumption, or disorders not yet established.
目前关于人口统计学特征、具体临床表现与中性粒细胞功能障碍之间的关系的数据较少,这使得医生难以确定哪些临床症状和体征是潜在吞噬细胞功能障碍的指征。
分析了我们实验室在过去 21 年中所有因复发性化脓性感染而被转介至实验室进行白细胞功能检查的成年和儿科患者的数据。中性粒细胞功能研究包括趋化作用、超氧化物产生(SOP)、杀菌活性(BA),以及疑似原发性吞噬细胞功能障碍(PPD)时的特定研究。
在 998 例患者中,发现 33.6%的患者存在中性粒细胞功能障碍;其中,趋化作用异常占 16.6%,SOP 异常占 6%,BA 异常占 24.5%。患者年龄越小,受累的器官系统越多,发现吞噬功能障碍的可能性就越大。趋化作用异常与复发性口腔溃疡、与 IgE 升高相关的感染以及脓性上呼吸道感染相关。SOP 和 BA 异常与深部脓肿、复发性淋巴结炎、脓毒症以及骨、关节和中枢神经系统感染相关。鉴定出 5.7%的患者存在 PPD,4.8%的患者存在慢性肉芽肿病,0.3%的患者存在中性粒细胞葡萄糖-6-磷酸脱氢酶缺乏症,0.4%的患者存在白细胞黏附缺陷 1 型,0.2%的患者存在髓过氧化物酶缺乏症。吞噬功能评估有助于诊断高免疫球蛋白 E 综合征(n=21)和 Chediak-Higashi 综合征(n=3)。
在复发性化脓性感染患者中,发现 5.7%的患者存在 PPD;其余患者的吞噬功能障碍可能与持续感染、药物消耗或尚未确定的疾病的有害影响有关。