Matsuda K, Tsutsumi H, Okamoto Y, Chiba C
Department of Pediatrics, Sapporo Medical University School of Medicine, Japan.
Clin Diagn Lab Immunol. 1995 May;2(3):322-4. doi: 10.1128/cdli.2.3.322-324.1995.
Cytokine (interleukin 6 [IL-6] and tumor necrosis factor alpha [TNF-alpha]) activity in nasopharyngeal secretions of 21 infants and children (19 days to 16 months old) infected with primary respiratory syncytial virus was determined by an enzyme-linked immunosorbent assay. IL-6 and TNF-alpha were detectable in 100% (21 of 21) and 67% (14 of 21) of cases during the course of infection, respectively. Generally, TNF-alpha activity was high in the acute phase and declined thereafter, sometimes to undetectable levels. IL-6 activity was also highest in the acute phase and declined thereafter in infants younger than 5 months, while in patients older than 5 months, it-increased during the course of the disease to peak in the early convalescent phase. These observations suggest that inflammatory cytokines are produced in vivo in infants and children in response to primary respiratory syncytial virus infection and may be involved in disease pathogenesis. However, the mechanism of induction of cytokines may be different for infants and children in different age groups.
采用酶联免疫吸附试验测定了21例感染原发性呼吸道合胞病毒的婴幼儿(19天至16个月大)鼻咽分泌物中的细胞因子(白细胞介素6 [IL-6]和肿瘤坏死因子α [TNF-α])活性。在感染过程中,分别有100%(21例中的21例)和67%(21例中的14例)的病例检测到IL-6和TNF-α。一般来说,TNF-α活性在急性期较高,此后下降,有时降至检测不到的水平。IL-6活性在急性期也最高,5个月以下的婴儿此后下降,而在5个月以上的患者中,它在疾病过程中升高,在恢复期早期达到峰值。这些观察结果表明,炎症细胞因子在婴幼儿体内因原发性呼吸道合胞病毒感染而产生,可能参与疾病发病机制。然而,不同年龄组的婴幼儿细胞因子诱导机制可能不同。