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Volume 3 Supplement 1

ESICM LIVES 2015

  • Poster presentation
  • Open Access

T-helper cell polarisation following severe polytrauma

  • 1, 2, 3,
  • 2, 3,
  • 2,
  • 1,
  • 1, 3,
  • 2 and
  • 1, 3
Intensive Care Medicine Experimental20153 (Suppl 1) :A848

https://doi.org/10.1186/2197-425X-3-S1-A848

  • Published:

Keywords

  • Intensive Care Unit
  • Nosocomial Infection
  • Intensive Care Unit Stay
  • Royal College
  • White Cell Count

Introduction

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].

Objectives

1) To define alterations in TH cell subsets following severe blunt polytrauma.

Methods

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 [2] 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.

Results

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).

Figure 1

Figure 2

Conclusions

Severe polytrauma patients swiftly become lymphopenic. Although a failure to normalise this during the ICU stay correlates with higher mortality [3] 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.

Grant Acknowledgment

Royal College of Surgeons of England, Barts & the London Charity.

Authors’ Affiliations

(1)
Barts & the London School of Medicine, QMUL, William Harvey Research Institute, London, United Kingdom
(2)
Barts & the London School of Medicine, QMUL, Blizard Institute, London, United Kingdom
(3)
Barts Health NHS Trust, Trauma & Critical Care, London, United Kingdom

References

  1. 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.PubMedView ArticleGoogle Scholar
  2. Maecker HT, et al: Standardizing immunophenotyping for the Human Immunology Project. Nat Rev Immunol. 2012, 12: 191-200.PubMedPubMed CentralGoogle Scholar
  3. 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.PubMedPubMed CentralView ArticleGoogle Scholar

Copyright

© Torrance et al.; 2015

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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