Abstract

IntroductionMajor trauma is characterized by an overwhelming pro-inflammatory response and an accompanying anti-inflammatory response that lead to a state of immunosuppression, as observed after septic shock. Diminished monocyte Human Leukocyte Antigen DR (mHLA-DR) is a reliable marker of monocyte dysfunction and immunosuppression. The main objective of this study was to determine the relation between mHLA-DR expression in severe trauma patients and the development of sepsis.MethodsWe conducted a prospective observational study over 23 months in a trauma intensive care unit at a university hospital. Patients with an Injury Severity Score (ISS) over 25 and age over 18 were included. mHLA-DR was assessed by flow cytometry protocol according to standardized protocol. Mann-Whitney U-test for continuous non-parametric variables, independent paired t test for continuous parametric variables and chi-square test for categorical data were used.ResultsmHLA-DR was measured three times a week during the first 14 days. One hundred five consecutive severely injured patients were monitored (ISS 38 ± 17, SAPS II 37 ± 16). Thirty-seven patients (35%) developed sepsis over the 14 days post-trauma. At days 1-2, mHLA-DR was diminished in the whole patient population, with no difference with the development of sepsis. At days 3-4, a highly significant difference appeared between septic and non-septic patients. Non- septic patients showed an increase in mHLA-DR levels, whereas septic patients did not (13,723 ± 7,766 versus 9,271 ± 6,029 antibodies per cell, p = .004). Most importantly, multivariate logistic regression analysis, after adjustment for usual clinical confounders (adjusted OR 5.41, 95% CI 1.42-20.52), revealed that a slope of mHLA-DR expression between days1-2 and days 3-4 below 1.2 remained associated with the development of sepsis.ConclusionsMajor trauma induced an immunosuppression, characterized by a decrease in mHLA-DR expression. Importantly, after multivariate regression logistic analysis, persistent decreased expression was assessed to be in relation with the development of sepsis. This is the first study in trauma patients showing a link between the lack of immune recovery and the development of sepsis on the basis of the standardized protocol. Monitoring immune function by mHLA-DR measurement could be useful to identify trauma patients at a high risk of infection.

Highlights

  • Major trauma is characterized by an overwhelming pro-inflammatory response and an accompanying anti-inflammatory response that lead to a state of immunosuppression, as observed after septic shock

  • Patients admitted on a Saturday were excluded because monocyte Human Leukocyte Antigen DR (mHLA-DR) cannot be measured on day 1 or 2

  • Years Male, % (n) Injury Severity Score (ISS) Severe brain injury, % (n) Severe thoracic injury, % (n) SAPS Simplified Acute Physiology Score II (II) Delay for mean arterial pressure (MAP) >65 mm Hg, minutes Need for vasoactive support in emergency room, % (n) Prophylactic antibiotics administrated in emergency room, % (n) Sepsis-related Organ Failure Assessment (SOFA) score

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Summary

Introduction

Major trauma is characterized by an overwhelming pro-inflammatory response and an accompanying anti-inflammatory response that lead to a state of immunosuppression, as observed after septic shock. It is well established that any situation of injury or stress can induce a systemic inflammatory response that is often followed by an anti-inflammatory response [5,6,7] This compensatory feedback mechanism, which maintains inflammatory immune homeostasis, is believed to lower natural defenses against pathogens and contribute to a state of immunosuppression [8,9,10] and is known to occur in cases of sepsis, septic shock, burns, stroke, and injury and in patients undergoing major surgery. Such alterations might be directly responsible for a detrimental outcome in trauma patients and for lowering the resistance to nosocomial infections in patients who have survived initial resuscitation [7,8,9,11]

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