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Immunoparalysis and adverse outcomes from critical illness

Journal

PEDIATRIC CLINICS OF NORTH AMERICA
Volume 55, Issue 3, Pages 647-+

Publisher

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.pcl.2008.02.009

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Funding

  1. NHLBI NIH HHS [K08 HL085525, K08HL085525, K08 HL085525-02] Funding Source: Medline
  2. NICHD NIH HHS [UG1 HD083170] Funding Source: Medline

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Proper immunologic balance between pro- and anti-inflammatory forces is necessary for recovery from critical illness. Persistence of a marked compensatory anti-inflammatory innate immune response after an insult is termed immunoparalysis. Critically ill patients demonstrating prolonged, severe reductions in monocyte HLA-DR expression or ex vivo tumor necrosis factor a production are at high risk for nosocomial infection and death. Reversal of immunoparalysis can be accomplished through the administration of immunostimulatory agents or tapering of exogenous immunosuppression. Evidence suggests that this may be associated with improved clinical outcomes. Immune-monitoring protocols are needed to identify patients who may benefit from immunomodulatory trials.

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