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| Research article summary (published 30 Mar 1993): |
Leukocyte CD18 monoclonal antibody worsens endotoxemia and cardiovascular injury in canines with septic shock.
Full Abstract
We investigated the effects of a murine monoclonal antibody directed against the canine leukocyte CD11/18 adhesion complex (MAb R15.7) in a canine model of septic shock. Awake 2-yr-old purpose-bred beagles were studied 7 days before and 1, 2, 4, and 10 days after intraperitoneal placement of an Escherichia coli-infected fibrin clot. Starting 12 h before clot placement, animals received 0.5-1 mg/kg iv every 12 h (4 doses total) of either MAb R15.7 (MAb group, n = 8) or, as controls, murine serum protein (n = 8). After infected clot placement, all animals received antibiotic (ceftriaxne, 100 mg.kg-1.day-1 for 4 days). Two of eight control animals and four of eight MAb animals died (P = 0.4). During the first 8 h after clot placement, MAb animals, compared with control animals, had greater (P < 0.06) increases in serum endotoxin levels and higher (P < 0.05) neutrophil counts. Day 1 after clot placement, MAb animals, compared with control animals, had decreased (P < 0.05) central venous pressure and arterial pH and increased (P < 0.05) arterial lactate. Day 2 after clot placement, MAb animals, compared with control animals, had decreased (P < 0.05) cardiac index and mean arterial pressure. In summary, MAb R15.7, although associated with increased neutrophil counts, worsened serum endotoxemia, acidosis, and cardiovascular function in this canine model of septic shock. These data suggest that in septic shock, antibody directed against this leukocyte membrane protein complex may be harmful, possibly via impairment of normal leukocyte function.
Author information
Author/s: Eichacker, P Q (PQ); Hoffman, W D (WD); Farese, A (A); Danner, R L (RL); Suffredini, A F (AF); Waisman, Y (Y); Banks, S M (SM); Mouginis, T (T); Wilson, L (L); Rothlein, R (R);
Affiliation: Critical Care Medicine Department, National Institutes of Health, Bethesda 20892.
Journal and publication information
Publication Type: Journal Article
Journal: Journal of applied physiology (Bethesda, Md. : 1985) (J Appl Physiol), published in UNITED STATES. (Language: eng)
Reference: 1993-Apr; vol 74 (issue 4) : pp 1885-92
Dates: Created 1993/07/19; Completed 1993/07/19; Revised 2003/11/14;
PMID: 8099906, status: MEDLINE (last retrieval date: 2/18/2009, IMS Date: )
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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