Cj. Hauser et al., HUMAN PERIPHERAL MONONUCLEAR-CELLS DO NOT SHOW PROINFLAMMATORY PATTERNS OF CYTOKINE TRANSCRIPTION IN EARLY TRAUMA - A PRELIMINARY-REPORT, Shock, 4(4), 1995, pp. 247-250
Injury has been hypothesized to cause inflammation through systemic re
lease of lipopolysaccharide and pro-inflammatory cytokines, but this h
as proved difficult to demonstrate in humans. We looked for evidence o
f an inflammatory pattern of cytokine gene expression by peripheral bl
ood mononuclear cells (PBM) in six polytraumatized patients (ISS = 25
+/- 8) upon ER admission, and in six matched healthy controls. PBM tum
or necrosis factor (TNF)-alpha, interleukin (Il)-1 beta, IL-4, IL-6, I
L-10, and interferon (IFN)-gamma message was assessed by semi-quantita
tive reverse-transcription polymerase chain reaction. No increase in e
xpression of any of the pro-inflammatory cytokines (tumor necrosis fac
tor-alpha, IL-1 beta, or IL-6) was found after trauma, and IFN-gamma t
ended to decrease. Of the immunosuppressive cytokines, IL-10 expressio
n increased 5-fold (p<.05) but no change in IL-4 was discerned. This p
attern is fundamentally different from the cytokine expression pattern
s expected with sepsis or exposure to lipopolysaccharide. These findin
gs are inconsistent with the occurrence of systemic endotoxemia and su
bsequent global immunocyte activation early after trauma.