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Antimicrobial Agents and Chemotherapy, September 1999, p. 2170-2175, Vol. 43, No. 9
Microbiology Section,
Received 24 February 1999/Returned for modification 30 March
1999/Accepted 15 June 1999
The most widely used drug for treatment of candidiasis is
fluconazole (FCZ). Recently, a new derivative of 1,4-benzothiazine, compound FS5, was developed. FS5 had an appreciable protective effect
against murine candidiasis. The present study was designed to dissect
the antifungal mechanisms triggered by FS5 and to establish whether
this compound could enhance the antimicrobial abilities of natural
effector cells. The results show that intraperitoneal injection of FS5
in mice (i) induced an increase in circulating neutrophil levels
comparable to that observed in FCZ-treated mice; (ii) enhanced
phagocytosis and the killing activities of macrophages (M
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
A New Azole Derivative of 1,4-Benzothiazine
Increases the Antifungal Mechanisms of Natural Effector Cells
s) isolated
from the spleen or peritoneal cavity, with the latter effect
correlating with induction of nitric oxide synthesis and production by
M
s; and (iii) increased the levels of expression and synthesis of
tumor necrosis factor alpha. These results suggest that the
compound-induced synthesis of antimicrobial and proinflammatory molecules by heterogeneous M
populations is part of the beneficial effect of FS5 exerted against murine candidiasis.
*
Corresponding author. Mailing address: Microbiology
Section, Department of Experimental Medicine and Biochemical Sciences, University of Perugia, Via del Giochetto, 06122 Perugia, Italy. Phone:
39-075-585-3407. Fax: 39-075-585-3400. E-mail:
vecchiar{at}unipg.it.
Antimicrobial Agents and Chemotherapy, September 1999, p. 2170-2175, Vol. 43, No. 9
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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