Resumo (PT):
Efforts for the development of new therapeutics, essential for the control of leishmaniasis rely mainly on screening of potentially effective
compounds in pathogen growth/multiplication assays, both in vitro and in vivo. Screenings designed to closely reflect the situation in vivo are
currently labor-intensive and expensive, since they require intracellular amastigotes and animal models. Screenings designed to facilitate rapid testing
of a large number of drugs are not performed on the clinically relevant parasite stage, but the promastigotes. The ability to select transgenic
Leishmania expressing reporter proteins, such as the green fluorescent protein (GFP) or the luciferase, opened up new possibilities for the
development of drug screening tests. In this review we will focus on available methodologies for direct drug screening purposes against the
mammalian stage of the parasite, with emphasis on the future developments that could improve sensitivity, reliability, versatility and the throughput of the intracellular model screening.
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Keywords: Leishmania; Drug screening; Amastigote
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<a target="_blank" href="http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6TB7-4M7KB4C-1&_user=2460038&_coverDate=03%2F31%2F2007&_rdoc=3&_fmt=high&_orig=browse&_srch=doc-info(%23toc%235135%232007%23999439998%23644757%23FLA%23display%23Volume)&_cdi=5135&_sort=d&_docanchor=&_ct=15&_acct=C000057398&_version=1&_urlVersion=0&_userid=2460038&md5=0ed240b425f379f444a6a385ae9c042e"> texto integral</a>
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Abstract (EN):
Efforts for the development of new therapeutics, essential for the control of leishmaniasis rely mainly on screening of potentially effective
compounds in pathogen growth/multiplication assays, both in vitro and in vivo. Screenings designed to closely reflect the situation in vivo are
currently labor-intensive and expensive, since they require intracellular amastigotes and animal models. Screenings designed to facilitate rapid testing
of a large number of drugs are not performed on the clinically relevant parasite stage, but the promastigotes. The ability to select transgenic
Leishmania expressing reporter proteins, such as the green fluorescent protein (GFP) or the luciferase, opened up new possibilities for the
development of drug screening tests. In this review we will focus on available methodologies for direct drug screening purposes against the
mammalian stage of the parasite, with emphasis on the future developments that could improve sensitivity, reliability, versatility and the throughput of the intracellular model screening.
<br>
<br>
Keywords: Leishmania; Drug screening; Amastigote
<br>
<a target="_blank" href="http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6TB7-4M7KB4C-1&_user=2460038&_coverDate=03%2F31%2F2007&_rdoc=3&_fmt=high&_orig=browse&_srch=doc-info(%23toc%235135%232007%23999439998%23644757%23FLA%23display%23Volume)&_cdi=5135&_sort=d&_docanchor=&_ct=15&_acct=C000057398&_version=1&_urlVersion=0&_userid=2460038&md5=0ed240b425f379f444a6a385ae9c042e"> Full text</a>
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Language:
Portuguese
Type (Professor's evaluation):
Scientific