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Efficacy of Oral APX001 in a Murine Model of Cryptococcal Meningitis
BACKGROUND: APX001 is a first-in-class intravenous and orally available broad spectrum antifungal inhibitor of Gwt1, a protein involved in glycosylphosphatidylinositol anchor biosynthesis. This study evaluated efficacy of APX001, alone and in combination with fluconazole (FCN), in a mouse model of c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630770/ http://dx.doi.org/10.1093/ofid/ofx163.1225 |
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author | Schell, Wiley A Giamberardino, Charles Shaw, Karen J Perfect, John R |
author_facet | Schell, Wiley A Giamberardino, Charles Shaw, Karen J Perfect, John R |
author_sort | Schell, Wiley A |
collection | PubMed |
description | BACKGROUND: APX001 is a first-in-class intravenous and orally available broad spectrum antifungal inhibitor of Gwt1, a protein involved in glycosylphosphatidylinositol anchor biosynthesis. This study evaluated efficacy of APX001, alone and in combination with fluconazole (FCN), in a mouse model of cryptococcal meningitis. METHODS: Mice (10/group) infected via tail vein with Cryptococcus neoformans received APX001, FCN, both, or neither, for 7 days. APX001 was given orally as 390mg/kg thrice daily. FCN was given intraperitoneally as 80mg/kg/day. Brain and lung were cultured to determine tissue burden. Data were evaluated by unpaired t-test. RESULTS: In brain, the burden of C. neoformans in mice receiving combined therapy was 3.52 log lower than in untreated control mice. The burden in mice receiving APX001 alone was 0.78 log lower than in untreated mice. The burden in mice receiving FCN alone was 1.04 log lower than in untreated mice. In lung, the burden in mice receiving combined therapy was 1.84 log lower than in untreated control mice. The tissue burden for mice receiving APX001 alone was 1.58 log lower than in untreated mice. The tissue burden in mice receiving FCN alone was 1.3 log lower than untreated mice. CONCLUSION: Activity in murine brain: (i) Combined therapy of APX001 with FCN significantly inhibited growth of C. neoformans H99 compared with untreated control mice (P < 0.0001), and was significantly more active than monotherapy with APX001 or FCN (P < 0.0001 and P < 0.0003, respectively). (ii) APX001 and FCN each, alone, significantly inhibited growth of C. neoformans H99 in brain tissue compared with untreated control mice (P < 0.0001). Activity in murine lung: (i) Combined therapy of APX001 with FCN performed somewhat better than FCN alone (P = 0.0297), but no better than APX001 alone (P = 0.2500). (ii) APX001 and FCN each, alone, significantly inhibited growth of C. neformans H99 in lung tissue compared with untreated control mice (P < 0.0001). (iii) Significant potentiation of APX001 in combination with FCN in this model with C. neoformans H99 was observed within the brain, and further investigation is warranted to determine whether APX001 in combination with FCN has potential to be an effective oral regimen for treating cryptococcal meningitis. DISCLOSURES: K. J. Shaw, Amplyx Pharmaceuticals Inc.: Employee, Salary |
format | Online Article Text |
id | pubmed-5630770 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56307702017-11-07 Efficacy of Oral APX001 in a Murine Model of Cryptococcal Meningitis Schell, Wiley A Giamberardino, Charles Shaw, Karen J Perfect, John R Open Forum Infect Dis Abstracts BACKGROUND: APX001 is a first-in-class intravenous and orally available broad spectrum antifungal inhibitor of Gwt1, a protein involved in glycosylphosphatidylinositol anchor biosynthesis. This study evaluated efficacy of APX001, alone and in combination with fluconazole (FCN), in a mouse model of cryptococcal meningitis. METHODS: Mice (10/group) infected via tail vein with Cryptococcus neoformans received APX001, FCN, both, or neither, for 7 days. APX001 was given orally as 390mg/kg thrice daily. FCN was given intraperitoneally as 80mg/kg/day. Brain and lung were cultured to determine tissue burden. Data were evaluated by unpaired t-test. RESULTS: In brain, the burden of C. neoformans in mice receiving combined therapy was 3.52 log lower than in untreated control mice. The burden in mice receiving APX001 alone was 0.78 log lower than in untreated mice. The burden in mice receiving FCN alone was 1.04 log lower than in untreated mice. In lung, the burden in mice receiving combined therapy was 1.84 log lower than in untreated control mice. The tissue burden for mice receiving APX001 alone was 1.58 log lower than in untreated mice. The tissue burden in mice receiving FCN alone was 1.3 log lower than untreated mice. CONCLUSION: Activity in murine brain: (i) Combined therapy of APX001 with FCN significantly inhibited growth of C. neoformans H99 compared with untreated control mice (P < 0.0001), and was significantly more active than monotherapy with APX001 or FCN (P < 0.0001 and P < 0.0003, respectively). (ii) APX001 and FCN each, alone, significantly inhibited growth of C. neoformans H99 in brain tissue compared with untreated control mice (P < 0.0001). Activity in murine lung: (i) Combined therapy of APX001 with FCN performed somewhat better than FCN alone (P = 0.0297), but no better than APX001 alone (P = 0.2500). (ii) APX001 and FCN each, alone, significantly inhibited growth of C. neformans H99 in lung tissue compared with untreated control mice (P < 0.0001). (iii) Significant potentiation of APX001 in combination with FCN in this model with C. neoformans H99 was observed within the brain, and further investigation is warranted to determine whether APX001 in combination with FCN has potential to be an effective oral regimen for treating cryptococcal meningitis. DISCLOSURES: K. J. Shaw, Amplyx Pharmaceuticals Inc.: Employee, Salary Oxford University Press 2017-10-04 /pmc/articles/PMC5630770/ http://dx.doi.org/10.1093/ofid/ofx163.1225 Text en © The Author 2017. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Schell, Wiley A Giamberardino, Charles Shaw, Karen J Perfect, John R Efficacy of Oral APX001 in a Murine Model of Cryptococcal Meningitis |
title | Efficacy of Oral APX001 in a Murine Model of Cryptococcal Meningitis |
title_full | Efficacy of Oral APX001 in a Murine Model of Cryptococcal Meningitis |
title_fullStr | Efficacy of Oral APX001 in a Murine Model of Cryptococcal Meningitis |
title_full_unstemmed | Efficacy of Oral APX001 in a Murine Model of Cryptococcal Meningitis |
title_short | Efficacy of Oral APX001 in a Murine Model of Cryptococcal Meningitis |
title_sort | efficacy of oral apx001 in a murine model of cryptococcal meningitis |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630770/ http://dx.doi.org/10.1093/ofid/ofx163.1225 |
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