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Antimicrobial Agents and Chemotherapy, March 1998, p. 545-549, Vol. 42, No. 3
Division of Infectious Diseases, Department
of Medicine, Vanderbilt University School of Medicine, Nashville,
Tennessee 37232-2605,1 and the
Department of Veterans Affairs Medical Center, Nashville,
Tennessee 37212-26372
Received 13 June 1997/Returned for modification 25 September
1997/Accepted 19 December 1997
The judicious use of perioperative antibiotic prophylaxis reduces
the infectious complications of surgery. However, increased bacterial resistance within hospitals may make antibiotic prophylaxis less effective in the future and alternative strategies are needed. New
immunomodulatory agents might prevent wound infections by stimulation
of the host immune system. To test this hypothesis, we administered
poly-[1-6]-
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Prophylactic Anti-Infective Activity of
Poly-[1-6]-
-D-Glucopyranosyl-[1-3]-
-D-Glucopyranose
Glucan in a Guinea Pig Model of Staphylococcal Wound
Infection
-D-glucopyranosyl-[1-3]-
-D-glucopyranose glucan (PGG glucan), which enhances neutrophil microbicidal activity, intravenously to guinea pigs in doses ranging from 0.015 to 4 mg/kg
of body weight on the day before, on the day of, and on the day after
intermuscular inoculation with methicillin-resistant strains of
Staphylococcus aureus and Staphylococcus
epidermidis. Abscesses were identified at 72 h, and median
infective doses (ID50) and statistical
significance were determined by logistic regression. Guinea
pigs receiving PGG glucan and inoculated with methicillin-resistant S. aureus and S. epidermidis exhibited ID50 of as much as 2.5- and
60-fold higher, respectively, than those of control guinea pigs not
receiving PGG glucan. Maximal protection was observed with a dose of 1 mg of PGG glucan per kg, and efficacy was reduced at higher as well as
at lower PGG glucan doses. Furthermore, a single dose of
PGG glucan given 24 h following bacterial inoculation was found to
be effective in preventing infection. We conclude that PGG glucan
reduces the risk of staphylococcal abscess formation. Neutrophil-activating agents are a novel means of prophylaxis against
surgical infection and may be less likely than antibiotics to be
affected adversely by the increasing antibiotic resistance of
nosocomial pathogens.
*
Corresponding author. Mailing address: Division of
Infectious Diseases, A-3310 MCN, Vanderbilt University Medical Center, Garland and 21st Ave. South, Nashville, TN 37232-2605. Phone: (615)
327-4751, ext. 5512. Fax: (615) 321-6327. E-mail:
kernodds{at}ctrvax.vanderbilt.edu.
Consultant for Alpha-Beta Technology, Inc., regarding clinical
trials of PGG glucan in surgery.
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