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Merck
  • Ultrasensitive real-time PCR for the clinical management of visceral leishmaniasis in HIV-Infected patients.

Ultrasensitive real-time PCR for the clinical management of visceral leishmaniasis in HIV-Infected patients.

The American journal of tropical medicine and hygiene (2013-05-01)
Israel Molina, Roser Fisa, Cristina Riera, Vicenç Falcó, Aleix Elizalde, Fernando Salvador, Manuel Crespo, Adrian Curran, Paulo López-Chejade, Silvia Tebar, Santiago Pérez-Hoyos, Esteban Ribera, Albert Pahissa
摘要

Molecular methods have been proposed as an alternative tool for the diagnosis of visceral leishmaniasis (VL), but no data are available regarding use for monitoring clinical outcome. A prospective cohort study of human immunodeficiency virus-(HIV) and VL-coinfected patients was conducted in a university-affiliated hospital in Barcelona, Spain. Leishmania parasite load was monitored using a real-time polymerase chain reaction (PCR) at baseline and every 3 months. Cutoff values for PCR were determined using receiver operating characteristic (ROC) curves. Overall, 37 episodes were analyzed, and 25 of these episodes were considered as relapsing episodes. A significant decrease of parasite load measured 3 months after treatment could predict the clinical evolution of VL. A parasite load over 0.9 parasites/mL measured 12 months after treatment could predicts relapse with a sensitivity of 100% and a specificity of 90.9%. Monitoring parasite load by an ultrasensitive quantitative Leishmania PCR is useful to predict the risk of relapse after a VL episode in HIV-infected patients.

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Sigma-Aldrich
两性霉素 B 溶液, 250 μg/mL in deionized water, 0.1 μm filtered, BioReagent, suitable for cell culture
Sigma-Aldrich
两性霉素B,可溶, powder, γ-irradiated, BioXtra, suitable for cell culture
Sigma-Aldrich
两性霉素B 来源于链霉菌 属, ~80% (HPLC), powder
Sigma-Aldrich
两性霉素B 来源于链霉菌 属, BioReagent, suitable for cell culture, ~80% (HPLC)
两性霉素 B, European Pharmacopoeia (EP) Reference Standard