In Vivo Interferon-γ Therapy Augments the In Vitro Ability of Chronic Granulomatous Disease Neutrophils to Damage Aspergillus Hyphae
During the recently completed double-blind, placebo-controlled, randomized trial of recombinant interferon-γ (rIFN-γ)therapy in chronic granulomatous disease (CGO), a metabolic assay of neutrophil damage to Aspergillus fumigatus hyphae was used to monitor neutrophil function before and during therap...
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Published in | The Journal of infectious diseases Vol. 163; no. 4; pp. 849 - 852 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Chicago, IL
University Chicago Press
01.04.1991
University of Chicago Press |
Subjects | |
Online Access | Get full text |
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Summary: | During the recently completed double-blind, placebo-controlled, randomized trial of recombinant interferon-γ (rIFN-γ)therapy in chronic granulomatous disease (CGO), a metabolic assay of neutrophil damage to Aspergillus fumigatus hyphae was used to monitor neutrophil function before and during therapy. In this assay, 5 × 104 conidia that had germinated into hyphae were exposed to 5 × 105, 15 × 105, or 50 × 105 CGD neutrophils. By analysis of variance, neutrophils from patients on rIFN-γ were found to produce significantly more damage to hyphae than those from the placebo group (P < .01). In subgroup analysis, this effect was best seen in the hyphae exposed to 50 × 105 CGD neutrophils, where neutrophils from patients receiving rIFN-γ produced significantly more damage to the hyphae than those from the placebo group (P < .05). In vivo rIFN-γ therapy improves the ability of CGD neutrophils to damage Aspergillus fumigatus hyphae in an in vitro assay. |
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Bibliography: | istex:08E6017428B13053C639B26A2257CD088E760242 Reprints or correspondence: Dr. John H. Rex, Bldg. 10, Room 11N107, National Institutes of Health, Bethesda, MD 20892. ark:/67375/HXZ-SB6VF637-S ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-News-3 |
ISSN: | 0022-1899 1537-6613 |
DOI: | 10.1093/infdis/163.4.849 |