- Poster presentation
- Open Access
T-helper cell polarisation following severe polytrauma
Intensive Care Medicine Experimental volume 3, Article number: A848 (2015)
Severe polytrauma induces an immunosuppressive response and is associated with a very high incidence of nosocomial infections. Previous studies have inferred that this detrimental immune response results from polarisation of the T helper (Th) response towards an anti-inflammatory, TH2 dominated, response at the expense of a bactericidal, Th1 response .
1) To define alterations in TH cell subsets following severe blunt polytrauma.
Patients presenting to the emergency department within 2 hours of severe polytrauma were eligible if intubated either at the scene or in ED. Isolated head injuries and those not expected to survive 24 hours were excluded. EDTA anti-coagulated blood was drawn at 0hr (within 2 hours of injury), at 24 and 72hrs. Samples were immediately lysed, washed, stained and analysed using a standardised human 8-colour TH 1, 2 & 17 panel  on an LSR II flow cytometer. A paired white cell count differential was obtained at each sampling point. Patients were followed until discharge or death. Data were analysed using non-parametric statistics, with results presented as median and IQR.
15 consecutive severe polytrauma patients requiring Intensive Care Unit (ICU) admission were recruited. Demographic and clinical data are outlined in Figure 1. Twelve (80%) lymphocytosis (3.3x109/L, 2.5 - 4.4x109/L) (Figyre 2A). At 72 hours leukocytes had fallen (P < 0.01, figure 2A) such that 6 (54%) of those surviving were lymphopenic (0.9x109/L, 0.6 - 1.2x109/L). Circulating CD4+ (P = 0.01; Figure 2B) and CD4+CD25+ (P < 0.05) lymphocytes increased over 72 hours. When expressed as a percentage of total circulating lymphocytes no significant change in the proportions of the TH 1, 2 & 17 subpopulations was detected (Figure 2C-E).
Severe polytrauma patients swiftly become lymphopenic. Although a failure to normalise this during the ICU stay correlates with higher mortality  our study of TH cell subtypes demonstrates no evidence of a switch to a detrimental anti-inflammatory TH2 subtype at the expense of the potentially protective bactericidal TH1 subtype.
Royal College of Surgeons of England, Barts & the London Charity.
Marik PE, Flemmer M: The immune response to surgery and trauma: Implications for treatment. J Trauma Acute Care Surg. 2012, 73: 801-8. 10.1097/TA.0b013e318265cf87.
Maecker HT, et al: Standardizing immunophenotyping for the Human Immunology Project. Nat Rev Immunol. 2012, 12: 191-200.
Heffernan DS, et al: Failure to normalize lymphopenia following trauma is associated with increased mortality, independent of the leukocytosis pattern. Crit Care. 2012, 16: R12-10.1186/cc11157.
About this article
Cite this article
Torrance, H., Brohi, K., Warnes, G. et al. T-helper cell polarisation following severe polytrauma. ICMx 3, A848 (2015) doi:10.1186/2197-425X-3-S1-A848
- Intensive Care Unit
- Nosocomial Infection
- Intensive Care Unit Stay
- Royal College
- White Cell Count