Krause P J, Maderazo E G, Scroggs M
Pediatrics. 1982 Feb;69(2):184-7.
Polymorphonuclear neutrophil (PMN) adherence to glass and nylon wool was examined in 19 healthy term newborns, 19 normal children aged 2 weeks to 17 years, and 33 adults in good health who were taking no medication. Using a whole blood glass adherence assay, neonatal PMN adherence (0.18 +/- 0.16%) was significantly less than PMN adherence in children (7.4 +/- 4.0%, P less than .0001) and in adults (16.0 +/- 4.5%, P less than .0001). Similar results were obtained when separated neonatal and adult PMNs were used with both glass and nylon wool column adherence assays, indicating that decreased neonatal PMN adherence is due to a cellular defect. In other experiments there was significantly greater reduction in adherence of separated PMNs with addition of neonatal serum than with adult serum, indicating that a humoral inhibitor also contributes to decreased adherence of neonatal PMNs. Decreased neonatal PMN adherence may be one cause of the increased susceptibility of neonates to serious bacterial infections.
对19名健康足月儿、19名年龄在2周龄至17岁的正常儿童以及33名未服用任何药物的健康成年人,检测了多形核中性粒细胞(PMN)对玻璃和尼龙棉的黏附情况。采用全血玻璃黏附试验,新生儿PMN黏附率(0.18±0.16%)显著低于儿童(7.4±4.0%,P<0.0001)和成年人(16.0±4.5%,P<0.0001)。当使用分离出的新生儿和成年人PMN进行玻璃和尼龙棉柱黏附试验时,得到了相似的结果,表明新生儿PMN黏附率降低是由于细胞缺陷所致。在其他实验中,加入新生儿血清后分离出的PMN黏附率的降低幅度显著大于加入成人血清后的降低幅度,表明一种体液抑制剂也导致了新生儿PMN黏附率的降低。新生儿PMN黏附率降低可能是新生儿对严重细菌感染易感性增加的原因之一。