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Soluble cytokine receptors and receptor antagonists are sequentially released after trauma
M Cinat1, K Waxman, N D Vaziri
1Department of Surgery, University of California Irvine Medical Center, Orange 92668, USA.
Abstract:
Cytokine receptors and receptor antagonists (RAs) have been identified in trauma patients. We hypothesized that after traumatic injury, a sequential release of soluble cytokine receptors and RAs may exist that mirrors the release of the primary cytokines themselves. Twenty-two patients were included in the study: 14 males and 8 females. The mean age was 30.1 +/- 12.5 (range, 19 to 71), and the mean Injury Severity Score was 28.7 +/- 12.6 (range, 4 to 57). There were 15 survivors and 7 nonsurvivors. Samples were collected on arrival to the emergency department and at serial intervals for up to 7 days. Monoclonal antibody enzyme-linked immunosorbent assay kits to tumor necrosis factor (TNF), soluble TNF-receptor (sTNF-R) 55 kd and 75 kd, interleukin (IL)-1 and IL-1 RA, and IL-2 and IL-2r were used. Sera from 22 healthy individuals were used as normal controls. No TNF, IL-1, or IL-2 could be detected in any patient sera after injury. Control levels for the soluble cytokine receptors and RAs were as follows: sTNF-R 55 kd, 607 +/- 89 pg/mL; sTNF-R 75 kd, 2,141 +/- 169 pg/mL; IL-1 RA, 291 +/- 35 pg/mL; and IL-2r, 426 +/- 53 U/mL. In trauma patients, both 55 kd and 75 kd sTNF-R were significantly elevated on arrival to the emergency department, with values of 2,441 +/- 506 pg/mL (p < 0.001) and 4,736 +/- 537 pg/mL (p < 0.001), respectively.(ABSTRACT TRUNCATED AT 250 WORDS)
Insights
Trauma patients show elevated levels of soluble tumor necrosis factor receptors (sTNF-R) upon emergency department arrival. This suggests a potential sequential release pattern of these receptors following traumatic injury.
Area of Science:
- Immunology
- Trauma Medicine
- Biochemistry
Background:
- Cytokine receptors and receptor antagonists (RAs) are implicated in trauma response.
- The sequential release of cytokines after injury is a known phenomenon.
- The dynamic changes in soluble cytokine receptors and RAs post-trauma require further investigation.
Purpose of the Study:
- To investigate the hypothesis that soluble cytokine receptors and RAs are sequentially released after traumatic injury.
- To quantify the levels of specific soluble cytokine receptors and RAs in trauma patients.
- To compare these levels to healthy controls and analyze their dynamics over time.
Main Methods:
- Enzyme-linked immunosorbent assay (ELISA) kits were used to measure levels of tumor necrosis factor (TNF), soluble TNF-receptors (sTNF-R) 55 kd and 75 kd, interleukin (IL)-1, IL-1 RA, IL-2, and IL-2r.
- Sera were collected from 22 trauma patients on arrival and serially for up to 7 days.
- Sera from 22 healthy individuals served as normal controls.
Main Results:
- No detectable levels of TNF, IL-1, or IL-2 were found in patient sera post-injury.
- Both 55 kd and 75 kd sTNF-R were significantly elevated in trauma patients upon emergency department arrival compared to controls (p < 0.001).
- Elevated sTNF-R levels were 2,441 +/- 506 pg/mL for 55 kd and 4,736 +/- 537 pg/mL for 75 kd.
Conclusions:
- Traumatic injury leads to a significant and immediate elevation of soluble TNF receptors.
- The findings support the hypothesis of a sequential release of soluble cytokine receptors post-trauma.
- Further research is warranted to explore the clinical implications of these early receptor changes in trauma care.
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