Abstract |
Macrophage colony-stimulating factor ( M-CSF) given subcutaneously at a dose of 2.5 mg/kg of body weight (4.75 x 10(6) U/kg) to CD-1 male mice 8 to 12 weeks old was found to enhance significantly the fungistasis of bronchoalveolar macrophages (BAM) against Cryptococcus neoformans. When M-CSF was given 1, 3, 7, 9, or 13 days before an ex vivo challenge with C. neoformans, fungistasis was increased (P ranged from < 0.05 to < 0.001) compared with that induced by control BAM. A maximum effect was seen by days 1 and 3 after administration of M-CSF. Twenty-one days after M-CSF, BAM did not produce significantly enhanced fungistasis. M-CSF also significantly enhances the fungistatic effect of peritoneal macrophages (PM) if given 1, 3, and 7 days prior to testing against C. neoformans in comparison with control PM (P ranged from < 0.05 to < 0.001). PM did not produce enhanced fungistasis 9 or 13 days after administration of M-CSF. These studies demonstrating in vivo enhancement of anticryptococcal activity of macrophages with M-CSF provide a rationale for in vivo use of M-CSF to enhance resistance to infection with C. neoformans.
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Authors | F Nassar, E Brummer, D A Stevens |
Journal | Antimicrobial agents and chemotherapy
(Antimicrob Agents Chemother)
Vol. 38
Issue 9
Pg. 2162-4
(Sep 1994)
ISSN: 0066-4804 [Print] United States |
PMID | 7811036
(Publication Type: Journal Article)
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Chemical References |
- Macrophage Colony-Stimulating Factor
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Topics |
- Animals
- Cryptococcosis
(drug therapy, immunology)
- Cryptococcus neoformans
(drug effects, growth & development, immunology)
- Injections, Subcutaneous
- Kinetics
- Macrophage Colony-Stimulating Factor
(pharmacology)
- Macrophages, Alveolar
(drug effects, microbiology)
- Macrophages, Peritoneal
(drug effects, microbiology)
- Male
- Mice
- Mice, Inbred Strains
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