Alternatives to amphotericin B for Candida rugosa infection
Autor(a) principal: | |
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Data de Publicação: | 2004 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
dARK ID: | ark:/48912/0013000006jj2 |
DOI: | 10.1093/jac/dkh335 |
Texto Completo: | http://dx.doi.org/10.1093/jac/dkh335 http://repositorio.unifesp.br/handle/11600/27842 |
Resumo: | Objective: Amphotericin B failure is frequently seen in patients with candidaemia caused by Candida rugosa. We evaluated amphotericin 13, fluconazole, posaconazole and voriconazole as alternative treatments against infection in mice with two isolates of C. rugosa.Methods: Neutropenic mice were inoculated intravenously with C. rugosa. Amphotericin 13, fluconazole, posaconazole and voriconazole were administered for 7 days after infection. Efficacy of the antifungal treatment was assessed by survival and tissue burden of C. rugosa.Results: All of the four drugs significantly prolonged survival over controls. With both isolates, kidney counts were reduced significantly below controls for amphotericin B, fluconazole and posaconazole. However, voriconazole was less effective than the other antifungals.Conclusion: Despite poor clinical response to amphotericin B, in vivo data indicate that amphotericin B increases organ clearance and survival over untreated controls. However, although voriconazole improved survival over controls, increased tissue clearance was not seen. This discrepancy may be caused by rapid clearance of voriconazole in mice. These studies suggest fluconazole, posaconazole or voriconazole may be useful alternatives to amphotericin B in therapy of C. rugosa infection. |
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Alternatives to amphotericin B for Candida rugosa infectionmurine modelantifungalsC. rugosaObjective: Amphotericin B failure is frequently seen in patients with candidaemia caused by Candida rugosa. We evaluated amphotericin 13, fluconazole, posaconazole and voriconazole as alternative treatments against infection in mice with two isolates of C. rugosa.Methods: Neutropenic mice were inoculated intravenously with C. rugosa. Amphotericin 13, fluconazole, posaconazole and voriconazole were administered for 7 days after infection. Efficacy of the antifungal treatment was assessed by survival and tissue burden of C. rugosa.Results: All of the four drugs significantly prolonged survival over controls. With both isolates, kidney counts were reduced significantly below controls for amphotericin B, fluconazole and posaconazole. However, voriconazole was less effective than the other antifungals.Conclusion: Despite poor clinical response to amphotericin B, in vivo data indicate that amphotericin B increases organ clearance and survival over untreated controls. However, although voriconazole improved survival over controls, increased tissue clearance was not seen. This discrepancy may be caused by rapid clearance of voriconazole in mice. These studies suggest fluconazole, posaconazole or voriconazole may be useful alternatives to amphotericin B in therapy of C. rugosa infection.Univ Texas, Hlth Sci Ctr, Dept Med, Div Infect Dis, San Antonio, TX 78229 USAUniv Texas, Hlth Sci Ctr, Dept Pathol, San Antonio, TX 78229 USAUniv Autonoma Nuevo Leon, Fac Med, Dept Microbiol, Monterrey, MexicoUniversidade Federal de São Paulo, Div Infect Dis, São Paulo, BrazilUniversidade Federal de São Paulo, Div Infect Dis, São Paulo, BrazilWeb of ScienceOxford Univ PressUniv TexasUniv Autonoma Nuevo LeonUniversidade Federal de São Paulo (UNIFESP)Hernandez, S.Gonzalez, G. M.McCarthy, D. I.Colombo, Arnaldo Lopes [UNIFESP]Najvar, L. K.Bocanegera, R.Graybill, JR2016-01-24T12:37:16Z2016-01-24T12:37:16Z2004-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion477-480http://dx.doi.org/10.1093/jac/dkh335Journal of Antimicrobial Chemotherapy. Oxford: Oxford Univ Press, v. 54, n. 2, p. 477-480, 2004.10.1093/jac/dkh3350305-7453http://repositorio.unifesp.br/handle/11600/27842WOS:000223372100030ark:/48912/0013000006jj2engJournal of Antimicrobial Chemotherapyinfo:eu-repo/semantics/openAccesshttp://www.oxfordjournals.org/access_purchase/self-archiving_policyb.htmlreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2022-07-08T10:54:13Zoai:repositorio.unifesp.br/:11600/27842Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-12-11T20:01:10.532731Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Alternatives to amphotericin B for Candida rugosa infection |
title |
Alternatives to amphotericin B for Candida rugosa infection |
spellingShingle |
Alternatives to amphotericin B for Candida rugosa infection Alternatives to amphotericin B for Candida rugosa infection Hernandez, S. murine model antifungals C. rugosa Hernandez, S. murine model antifungals C. rugosa |
title_short |
Alternatives to amphotericin B for Candida rugosa infection |
title_full |
Alternatives to amphotericin B for Candida rugosa infection |
title_fullStr |
Alternatives to amphotericin B for Candida rugosa infection Alternatives to amphotericin B for Candida rugosa infection |
title_full_unstemmed |
Alternatives to amphotericin B for Candida rugosa infection Alternatives to amphotericin B for Candida rugosa infection |
title_sort |
Alternatives to amphotericin B for Candida rugosa infection |
author |
Hernandez, S. |
author_facet |
Hernandez, S. Hernandez, S. Gonzalez, G. M. McCarthy, D. I. Colombo, Arnaldo Lopes [UNIFESP] Najvar, L. K. Bocanegera, R. Graybill, JR Gonzalez, G. M. McCarthy, D. I. Colombo, Arnaldo Lopes [UNIFESP] Najvar, L. K. Bocanegera, R. Graybill, JR |
author_role |
author |
author2 |
Gonzalez, G. M. McCarthy, D. I. Colombo, Arnaldo Lopes [UNIFESP] Najvar, L. K. Bocanegera, R. Graybill, JR |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Univ Texas Univ Autonoma Nuevo Leon Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Hernandez, S. Gonzalez, G. M. McCarthy, D. I. Colombo, Arnaldo Lopes [UNIFESP] Najvar, L. K. Bocanegera, R. Graybill, JR |
dc.subject.por.fl_str_mv |
murine model antifungals C. rugosa |
topic |
murine model antifungals C. rugosa |
description |
Objective: Amphotericin B failure is frequently seen in patients with candidaemia caused by Candida rugosa. We evaluated amphotericin 13, fluconazole, posaconazole and voriconazole as alternative treatments against infection in mice with two isolates of C. rugosa.Methods: Neutropenic mice were inoculated intravenously with C. rugosa. Amphotericin 13, fluconazole, posaconazole and voriconazole were administered for 7 days after infection. Efficacy of the antifungal treatment was assessed by survival and tissue burden of C. rugosa.Results: All of the four drugs significantly prolonged survival over controls. With both isolates, kidney counts were reduced significantly below controls for amphotericin B, fluconazole and posaconazole. However, voriconazole was less effective than the other antifungals.Conclusion: Despite poor clinical response to amphotericin B, in vivo data indicate that amphotericin B increases organ clearance and survival over untreated controls. However, although voriconazole improved survival over controls, increased tissue clearance was not seen. This discrepancy may be caused by rapid clearance of voriconazole in mice. These studies suggest fluconazole, posaconazole or voriconazole may be useful alternatives to amphotericin B in therapy of C. rugosa infection. |
publishDate |
2004 |
dc.date.none.fl_str_mv |
2004-08-01 2016-01-24T12:37:16Z 2016-01-24T12:37:16Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1093/jac/dkh335 Journal of Antimicrobial Chemotherapy. Oxford: Oxford Univ Press, v. 54, n. 2, p. 477-480, 2004. 10.1093/jac/dkh335 0305-7453 http://repositorio.unifesp.br/handle/11600/27842 WOS:000223372100030 |
dc.identifier.dark.fl_str_mv |
ark:/48912/0013000006jj2 |
url |
http://dx.doi.org/10.1093/jac/dkh335 http://repositorio.unifesp.br/handle/11600/27842 |
identifier_str_mv |
Journal of Antimicrobial Chemotherapy. Oxford: Oxford Univ Press, v. 54, n. 2, p. 477-480, 2004. 10.1093/jac/dkh335 0305-7453 WOS:000223372100030 ark:/48912/0013000006jj2 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Antimicrobial Chemotherapy |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess http://www.oxfordjournals.org/access_purchase/self-archiving_policyb.html |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://www.oxfordjournals.org/access_purchase/self-archiving_policyb.html |
dc.format.none.fl_str_mv |
477-480 |
dc.publisher.none.fl_str_mv |
Oxford Univ Press |
publisher.none.fl_str_mv |
Oxford Univ Press |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
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UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
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1822219230623301632 |
dc.identifier.doi.none.fl_str_mv |
10.1093/jac/dkh335 |