TY - JOUR
T1 - Immunoglobulin E and eosinophil counts are increased after sepsis in trauma patients
AU - DiPiro, Joseph T.
AU - Howdieshell, Thomas R.
AU - Hamilton, Robert G.
AU - Mansberger, Arlie R.
PY - 1998/4/8
Y1 - 1998/4/8
N2 - Objectives: To determine the time course of plasma immunoglobulin E (IgE) concentration increases after traumatic injury, if increase IgE concentrations were related to clinical events or complications, and if increased peripheral eosinophil counts could be related to trauma, sepsis, or organ-specific complications. Design: Data relating to severity of injury, clinical complications, plasma concentrations of IgE, and peripheral eosinophil counts were prospectively collected. Setting: Trauma service, tertiary-care medical center. Patients: One hundred adult trauma patients admitted to the intensive care unit. Interventions: None. Measurements and Main Results: Plasma IgE concentrations increased in most patients. However, the greatest increases were observed in patients with sepals (p = .03), renal dysfunction (p = .04), or pneumonia (p = .02), IgE increases were not related to severity or mechanism of injury, allergy history, or age. The day of highest observed IgE concentration was related to the day of onset of sepsis (p = .012, r = .39), and occurred a mean of 3.8 days after sepsis. Most patients had increased peripheral eosinophil counts and eosinophil percentages of white blood cells during their intensive care unit stays. Eosinophil counts were greater in patients with sepals (p<.0001), severe sepsis (p<.0001), or pneumonia (p< .002). Conclusions: Increased IgE concentrations and eosinophil counts were found after sepals and do not appear to be related to the initial injury. Since IgE and eosinophil production are enhanced by interleukin-4 and interleukin-5, respectively, these findings suggest that T-helper lymphocyte type 2 cytokines are activated in response to sepsis after traumatic injury.
AB - Objectives: To determine the time course of plasma immunoglobulin E (IgE) concentration increases after traumatic injury, if increase IgE concentrations were related to clinical events or complications, and if increased peripheral eosinophil counts could be related to trauma, sepsis, or organ-specific complications. Design: Data relating to severity of injury, clinical complications, plasma concentrations of IgE, and peripheral eosinophil counts were prospectively collected. Setting: Trauma service, tertiary-care medical center. Patients: One hundred adult trauma patients admitted to the intensive care unit. Interventions: None. Measurements and Main Results: Plasma IgE concentrations increased in most patients. However, the greatest increases were observed in patients with sepals (p = .03), renal dysfunction (p = .04), or pneumonia (p = .02), IgE increases were not related to severity or mechanism of injury, allergy history, or age. The day of highest observed IgE concentration was related to the day of onset of sepsis (p = .012, r = .39), and occurred a mean of 3.8 days after sepsis. Most patients had increased peripheral eosinophil counts and eosinophil percentages of white blood cells during their intensive care unit stays. Eosinophil counts were greater in patients with sepals (p<.0001), severe sepsis (p<.0001), or pneumonia (p< .002). Conclusions: Increased IgE concentrations and eosinophil counts were found after sepals and do not appear to be related to the initial injury. Since IgE and eosinophil production are enhanced by interleukin-4 and interleukin-5, respectively, these findings suggest that T-helper lymphocyte type 2 cytokines are activated in response to sepsis after traumatic injury.
KW - Eosinophils
KW - Immunoglobulin E
KW - Lymphocytes
KW - Pneumonia
KW - Renal dysfunction
KW - Sepsis
KW - Severe sepsis
KW - Trauma
UR - http://www.scopus.com/inward/record.url?scp=0031911430&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0031911430&partnerID=8YFLogxK
U2 - 10.1097/00003246-199803000-00016
DO - 10.1097/00003246-199803000-00016
M3 - Article
C2 - 9504573
AN - SCOPUS:0031911430
SN - 0090-3493
VL - 26
SP - 465
EP - 469
JO - Critical care medicine
JF - Critical care medicine
IS - 3
ER -