Despite significant progress in intensive care medicine, the mortality of s
eptic shock has not changed in recent years. Early recognition of subtle si
gns in favor of meningococcal sepsis, early antibiotic treatment, and aggre
ssive hemodynamic support remains the cornerstone of therapy of severe meni
ngococcal shock in children. Recent work has emphasized the role of genetic
polymorphisms in various systems to explain the most severe cases: anti-in
flammatory cytokine profile IL-10/TNF-alpha, elevated levels of plasminogen
activator inhibitor type-1, variants of the gene for mannose-binding lecti
n complement pathway. This may explain the disillusionment of pediatric int
ensivists, and the general failure of immunotherapy for sepsis. Reasonable
hope lies upon new meningococcal vaccines. (C) 2001 Editions scientifiques
et medicales Elsevier SAS.