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                  <mods:namePart>Mesa-Arango, Ana Cecilia</mods:namePart>
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               <mods:identifier type="citation">Front Microbiol. 2012 Aug 8;3:286. eCollection</mods:identifier>
               <mods:identifier type="doi">10.3389/fmicb.2012.00286</mods:identifier>
               <mods:identifier type="e-issn">1664-302X</mods:identifier>
               <mods:identifier type="issn">1664-302X</mods:identifier>
               <mods:identifier type="journal">Frontiers in microbiology</mods:identifier>
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               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/9133</mods:identifier>
               <mods:abstract>"Amphotericin B acts through pore formation at the cell membrane after binding to ergosterol" is an accepted dogma about the action mechanism of this antifungal, and this sentence is widely found in the literature. But after 60 years of investigation, the action mechanism of Amphotericin B is not fully elucidated. Amphotericin B is a polyene substance that is one of the most effective drugs for the treatment of fungal and parasite infections. As stated above, the first mechanism of action described was pore formation after binding to the ergosterol present in the membrane. But it has also been demonstrated that AmB induces oxidative damage in the cells. Moreover, amphotericin B modulates the immune system, and this activity has been related to the protective effect of the molecule, but also to its toxicity in the host. This review tries to provide a general overview of the main aspects of this molecule, and highlight the multiple effects that this molecule has on both the fungal and host cells.</mods:abstract>
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                  <mods:title>It only takes one to do many jobs: Amphotericin B as antifungal and immunomodulatory drug</mods:title>
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