CYTOKINE ELEVATIONS IN INFANTS WITH BACTERIAL AND ASEPTIC-MENINGITIS

被引:77
作者
DULKERIAN, SJ
KILPATRICK, L
COSTARINO, AT
MCCAWLEY, L
FEIN, J
CORCORAN, L
ZIRIN, S
HARRIS, MC
机构
[1] UNIV PENN, CHILDRENS HOSP, SCH MED, DIV NEONATOL, PHILADELPHIA, PA 19104 USA
[2] UNIV PENN, CHILDRENS HOSP, SCH MED, DIV ALLERGY, PHILADELPHIA, PA 19104 USA
[3] UNIV PENN, CHILDRENS HOSP, SCH MED, DIV INFECT DIS & IMMUNOL, PHILADELPHIA, PA 19104 USA
[4] UNIV PENN, CHILDRENS HOSP, SCH MED, DEPT PEDIAT, PHILADELPHIA, PA 19104 USA
[5] UNIV PENN, CHILDRENS HOSP, SCH MED, DEPT ANESTHESIA & CRIT CARE MED, PHILADELPHIA, PA 19104 USA
关键词
D O I
10.1016/S0022-3476(95)70199-0
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
We sought to determine whether the detection of cytokines, produced during the inflammatory response, would aid in the diagnosis of meningitis in young infants. We measured cerebrospinal fluid (CSF) and plasma levels of interleukin-6 (IL-6) and tumor necrosis factor (TNF) in 62 infants less than 6 months of age whose condition was evaluated for meningitis. Twenty infants had culture-proved meningitis, 22 had aseptic meningitis, and 20 control infants had no evidence of meningitis. The CSF IL-6 levels were elevated in all 20 infants with bacterial meningitis and in 9 of 22 infants with aseptic meningitis but were undetectable in all control subjects. Furthermore, CSF IL-6 levels were 10 times greater in infants with bacterial versus aseptic meningitis (p <0.001). Levels of TNF in CSF were detected in 12 of 20 infants with bacterial meningitis and were undetectable in infants with aseptic meningitis and in control infants (p <0.02). Plasma IL-6 and TNF levels were unreliable for the detection of meningitis in this patient population. We conclude that the presence of IL-6 in the CSF reliably identifies infants with meningitis and that the presence of CSF TNF is a highly specific indicator of bacterial meningeal inflammation.
引用
收藏
页码:872 / 876
页数:5
相关论文
共 27 条
  • [1] Klein, Feigin, McCracken, Et al., Report of the taskforce on diagnosis and management of meningitis, Pediatrics, 78, pp. 959-982, (1986)
  • [2] Tunkel, Scheld, Pathogenesis and pathophysiology of bacterial meningitis, Annu Rev Med, 44, pp. 103-120, (1993)
  • [3] Saukkonen, Sande, Cioffe, Et al., The role of cytokines in the generation of inflammation and tissue damage in experimental gram-positive meningitis, J Exp Med, 171, pp. 439-448, (1990)
  • [4] Ohga, Aoki, Okada, Et al., Cerebrospinal fluid concentrations of interleukin-1β, tumor necrosis factor-alpha, and interferon gamma in bacterial meningitis, Arch Dis Child, 70, pp. 123-125, (1994)
  • [5] Teti, Mancuso, Tomasello, Chiofalo, Production of tumor necrosis factor-alpha and interleukin-6 in mice infected with group B streptococci, Circ Shock, 38, pp. 138-144, (1992)
  • [6] Aggarwal, Kohr, Hass, Et al., Human tumor necrosis factor: production, [purification and characterization], J Biol Chem, 260, pp. 2345-2354, (1985)
  • [7] Beutler, Cerami, Cachectin: more than a tumor necrosis factor, N Engl J Med, 316, pp. 379-385, (1987)
  • [8] Helfgott, Tatter, Santhanam, Et al., Multiple forms of IFN-β<sub>2</sub>/IL-6 in serum and body fluids during acute bacterial infection, J Immunol, 142, pp. 948-953, (1989)
  • [9] Houssiau, Bukasa, Sindic, Van Damme, Van Snick, Elevated levels of 26K human hybridoma growth factor (interleukin-6) in cerebrospinal fluid of patients with acute infection of the central nervous system, Clin Exp Immunol, 71, pp. 320-323, (1988)
  • [10] Tracey, Beutler, Lowry, Et al., Shock and tissue injury induced by recombinant human cachectin, Science, 234, pp. 470-474, (1986)