Literature DB >> 8722846

The future of antifungal therapy.

J R Graybill1.   

Abstract

In the late 1970s the options for systemic antifungal therapy doubled with the addition of intravenous miconazole and oral ketoconazole to the two previously available agents, amphotericin B and flucytosine. The 1980s ushered in the next generation of triazole antifungals, fluconazole and itraconazole. These are the present-day mainstays of treatment for some of the most serious systemic fungal infections. However, the increase in the numbers and types of fungal pathogens, and especially the emergence of azole-resistant fungi, have prompted a continuing search for new therapeutic options. This search has yielded more-potent triazole antifungals, new vehicles for both polyenes and triazoles, and entirely new classes of agents such as the echinocandin derivatives; in addition, it has prompted the evaluation of new combinations of present-day antifungals and exploration of the use of immunomodulators for treatment of fungal infections. Rapid developments in molecular mycology are permitting a concentrated search for more targets for antifungals. We are entering a new era of antifungal therapy in which we will continue to be challenged by systemic fungal diseases but will have greatly expanded options for treatment.

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Year:  1996        PMID: 8722846     DOI: 10.1093/clinids/22.supplement_2.s166

Source DB:  PubMed          Journal:  Clin Infect Dis        ISSN: 1058-4838            Impact factor:   9.079


  9 in total

Review 1.  Antifungal prophylaxis during neutropenia and immunodeficiency.

Authors:  O Lortholary; B Dupont
Journal:  Clin Microbiol Rev       Date:  1997-07       Impact factor: 26.132

2.  Use of fluconazole in the treatment of non-AIDS cryptococcal meningitis.

Authors:  S J Antony; A Patel; J Leonard
Journal:  J Natl Med Assoc       Date:  1997-10       Impact factor: 1.798

3.  Compartmental pharmacokinetics and tissue drug distribution of the pradimicin derivative BMS 181184 in rabbits.

Authors:  A H Groll; T Sein; V Petraitis; R Petraitiene; D Callender; C E Gonzalez; N Giri; J Bacher; S Piscitelli; T J Walsh
Journal:  Antimicrob Agents Chemother       Date:  1998-10       Impact factor: 5.191

4.  Ocular distribution of intravenously administered lipid formulations of amphotericin B in a rabbit model.

Authors:  David Goldblum; Kaspar Rohrer; Beatrice E Frueh; Regula Theurillat; Wolfgang Thormann; Stefan Zimmerli
Journal:  Antimicrob Agents Chemother       Date:  2002-12       Impact factor: 5.191

5.  Pentamidine inhibition of group I intron splicing in Candida albicans correlates with growth inhibition.

Authors:  K E Miletti; M J Leibowitz
Journal:  Antimicrob Agents Chemother       Date:  2000-04       Impact factor: 5.191

6.  Reduction in the nephrotoxicity of amphotericin B when administered in 20% intralipid.

Authors:  S Salama; C Rotstein
Journal:  Can J Infect Dis       Date:  1997-05

7.  Compartmental pharmacokinetics and tissue distribution of the antifungal echinocandin lipopeptide micafungin (FK463) in rabbits.

Authors:  A H Groll; D Mickiene; V Petraitis; R Petraitiene; K H Ibrahim; S C Piscitelli; I Bekersky; T J Walsh
Journal:  Antimicrob Agents Chemother       Date:  2001-12       Impact factor: 5.191

Review 8.  Current and emerging azole antifungal agents.

Authors:  D J Sheehan; C A Hitchcock; C M Sibley
Journal:  Clin Microbiol Rev       Date:  1999-01       Impact factor: 26.132

9.  In vitro drug interaction modeling of combinations of azoles with terbinafine against clinical Scedosporium prolificans isolates.

Authors:  Joseph Meletiadis; Johan W Mouton; Jacques F G M Meis; Paul E Verweij
Journal:  Antimicrob Agents Chemother       Date:  2003-01       Impact factor: 5.191

  9 in total

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