B and I
B
in peripheral blood mononuclear cells of trauma patients


* Département de Physiopathologie, Institut Pasteur, 75724 Paris Cedex 15, France, and
Département dAnesthésie Réanimation, Hôpital du Kremlin Bicêtre, 94275 Le Kremlin Bicêtre Cedex, France
Correspondence: Dr. Pierre Moine, Département dAnesthésie Réanimation, Hôpital du Kremlin Bicêtre, 78 rue du général Leclerc, 94275 Le Kremlin Bicêtre Cedex, France. E-mail: pierre.moine1{at}fnac.net
Nuclear factor (NF)-
B expression and dimer characteristics were
studied in peripheral blood mononuclear cells (PBMCs) of major-trauma
patients and healthy controls. Analysis of PBMCs on days 1, 3, 5, and
10 after trauma revealed that expression of both p65p50 heterodimers
and p50p50 homodimers was significantly reduced compared with that in
controls. In vitro lipopolysaccharide (LPS) stimulation of PBMCs
induced NF-
B translocation. However, throughout the survey, p65p50
activation remained significantly lower in trauma patients than in
controls. After LPS stimulation in vitro, the p65p50/p50p50 ratio was
significantly lower in PBMCs from trauma patients than from healthy
controls. The ex vivo expression of I
B
was higher in PBMCs of
controls than of trauma patients. LPS did not induce I
B expression
in PBMCs from trauma patients, but strong induction was obtained with
staphylococci, suggesting that this defect is not universal and depends
on the nature of the activating signal. Although no direct correlation
was found between levels of interleukin-10 or transforming growth
factor-ß and NF-
B, these immunosuppressive cytokines were
significantly elevated in trauma patients by 10 days after admission.
The long-term low-basal and LPS-induced nuclear translocation of
NF-
B recalled long-term immunoparalysis observed in patients with
severe inflammatory stress such as trauma.
Key Words: lipopolysaccharide inflammation IL-10 immunoparalysis
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