Skip to main content
Archives of Disease in Childhood logoLink to Archives of Disease in Childhood
. 1999 Jan;80(1):74–76. doi: 10.1136/adc.80.1.74

Endothelial cell adhesion molecules in meningococcal disease

P Baines 1, O Marzouk 1, A Thomson 1, J Sills 1, F Riordan 1, C Hart 1
PMCID: PMC1717782  PMID: 10325765

Abstract

BACKGROUND—Endothelial damage is important in meningococcal disease. Cell adhesion molecules, including P selectin, E selectin, and intercellular cell adhesion molecule 1 (ICAM-1), are expressed by activated endothelium and then subsequently shed.
METHODS—ICAM-1, P selectin, and E selectin were measured on admission to hospital in children with meningococcal infections.
RESULTS—Concentrations of shed cell adhesion molecules are reported for 78 children. Eleven did not have meningococcal disease. Of the 67 with meningococcal disease, 40 had mild disease (Glasgow meningococcal septicaemia prognostic score (GMSPS) < 8) and 27had severe disease (GMSPS ⩾ 8). E selectin and ICAM-1 values were higher in those with meningococcal disease. The E selectin values in those with severe disease were higher than in those with mild disease. P selectin concentrations were not altered in meningococcal disease, but those who died had lower concentrations.
CONCLUSIONS—Endothelial activation in meningococcal disease is reflected by shed ICAM-1 and E selectin concentrations.



Full Text

The Full Text of this article is available as a PDF (90.2 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Boldt J., Muller M., Heesen M., Neumann K., Hempelmann G. G. Influence of different volume therapies and pentoxifylline infusion on circulating soluble adhesion molecules in critically ill patients. Crit Care Med. 1996 Mar;24(3):385–391. doi: 10.1097/00003246-199603000-00005. [DOI] [PubMed] [Google Scholar]
  2. Brandtzaeg P., Kierulf P., Gaustad P., Skulberg A., Bruun J. N., Halvorsen S., Sørensen E. Plasma endotoxin as a predictor of multiple organ failure and death in systemic meningococcal disease. J Infect Dis. 1989 Feb;159(2):195–204. doi: 10.1093/infdis/159.2.195. [DOI] [PubMed] [Google Scholar]
  3. Bruserud O., Akselen P. E., Bergheim J., Nesthus I. Serum concentrations of E-selectin, P-selectin, ICAM-1 and interleukin 6 in acute leukaemia patients with chemotherapy-induced leucopenia and bacterial infections. Br J Haematol. 1995 Oct;91(2):394–402. doi: 10.1111/j.1365-2141.1995.tb05309.x. [DOI] [PubMed] [Google Scholar]
  4. Cowley H. C., Heney D., Gearing A. J., Hemingway I., Webster N. R. Increased circulating adhesion molecule concentrations in patients with the systemic inflammatory response syndrome: a prospective cohort study. Crit Care Med. 1994 Apr;22(4):651–657. doi: 10.1097/00003246-199404000-00022. [DOI] [PubMed] [Google Scholar]
  5. Fortenberry J. D., Huber A. R., Owens M. L. Inotropes inhibit endothelial cell surface adhesion molecules induced by interleukin-1beta. Crit Care Med. 1997 Feb;25(2):303–308. doi: 10.1097/00003246-199702000-00019. [DOI] [PubMed] [Google Scholar]
  6. Frenette P. S., Wagner D. D. Adhesion molecules--Part II: Blood vessels and blood cells. N Engl J Med. 1996 Jul 4;335(1):43–45. doi: 10.1056/NEJM199607043350108. [DOI] [PubMed] [Google Scholar]
  7. Friedman G., Jankowski S., Shahla M., Goldman M., Rose R. M., Kahn R. J., Vincent J. L. Administration of an antibody to E-selectin in patients with septic shock. Crit Care Med. 1996 Feb;24(2):229–233. doi: 10.1097/00003246-199602000-00008. [DOI] [PubMed] [Google Scholar]
  8. Girardin E., Grau G. E., Dayer J. M., Roux-Lombard P., Lambert P. H. Tumor necrosis factor and interleukin-1 in the serum of children with severe infectious purpura. N Engl J Med. 1988 Aug 18;319(7):397–400. doi: 10.1056/NEJM198808183190703. [DOI] [PubMed] [Google Scholar]
  9. Jakobsen P. H., Morris-Jones S., Rønn A., Hviid L., Theander T. G., Elhassan I. M., Bygbjerg I. C., Greenwood B. M. Increased plasma concentrations of sICAM-1, sVCAM-1 and sELAM-1 in patients with Plasmodium falciparum or P. vivax malaria and association with disease severity. Immunology. 1994 Dec;83(4):665–669. [PMC free article] [PubMed] [Google Scholar]
  10. Klein N. J., Levin M., Strobel S., Finn A. Degradation of glycosaminoglycans and fibronectin on endotoxin-stimulated endothelium by adherent neutrophils: relationship to CD11b/CD18 and L-selectin expression. J Infect Dis. 1993 Apr;167(4):890–898. doi: 10.1093/infdis/167.4.890. [DOI] [PubMed] [Google Scholar]
  11. Newman W., Beall L. D., Carson C. W., Hunder G. G., Graben N., Randhawa Z. I., Gopal T. V., Wiener-Kronish J., Matthay M. A. Soluble E-selectin is found in supernatants of activated endothelial cells and is elevated in the serum of patients with septic shock. J Immunol. 1993 Jan 15;150(2):644–654. [PubMed] [Google Scholar]
  12. Ridings P. C., Windsor A. C., Jutila M. A., Blocher C. R., Fisher B. J., Sholley M. M., Sugerman H. J., Fowler A. A., 3rd A dual-binding antibody to E- and L-selectin attenuates sepsis-induced lung injury. Am J Respir Crit Care Med. 1995 Jul;152(1):247–253. doi: 10.1164/ajrccm.152.1.7541277. [DOI] [PubMed] [Google Scholar]
  13. Riordan F. A., Marzouk O., Thomson A. P., Sills J. A., Hart C. A. Proinflammatory and anti-inflammatory cytokines in meningococcal disease. Arch Dis Child. 1996 Nov;75(5):453–454. doi: 10.1136/adc.75.5.453. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Sakamaki F., Ishizaka A., Handa M., Fujishima S., Urano T., Sayama K., Nakamura H., Kanazawa M., Kawashiro T., Katayama M. Soluble form of P-selectin in plasma is elevated in acute lung injury. Am J Respir Crit Care Med. 1995 Jun;151(6):1821–1826. doi: 10.1164/ajrccm.151.6.7539327. [DOI] [PubMed] [Google Scholar]
  15. Sessler C. N., Windsor A. C., Schwartz M., Watson L., Fisher B. J., Sugerman H. J., Fowler A. A., 3rd Circulating ICAM-1 is increased in septic shock. Am J Respir Crit Care Med. 1995 May;151(5):1420–1427. doi: 10.1164/ajrccm.151.5.7735595. [DOI] [PubMed] [Google Scholar]
  16. Seth R., Raymond F. D., Makgoba M. W. Circulating ICAM-1 isoforms: diagnostic prospects for inflammatory and immune disorders. Lancet. 1991 Jul 13;338(8759):83–84. doi: 10.1016/0140-6736(91)90077-3. [DOI] [PubMed] [Google Scholar]
  17. Tan T. Q., Smith C. W., Hawkins E. P., Mason E. O., Jr, Kaplan S. L. Hematogenous bacterial meningitis in an intercellular adhesion molecule-1-deficient infant mouse model. J Infect Dis. 1995 Feb;171(2):342–349. doi: 10.1093/infdis/171.2.342. [DOI] [PubMed] [Google Scholar]
  18. Waage A., Halstensen A., Espevik T. Association between tumour necrosis factor in serum and fatal outcome in patients with meningococcal disease. Lancet. 1987 Feb 14;1(8529):355–357. doi: 10.1016/s0140-6736(87)91728-4. [DOI] [PubMed] [Google Scholar]

Articles from Archives of Disease in Childhood are provided here courtesy of BMJ Publishing Group

RESOURCES