BACKGROUND: Visceral leishmaniasis (VL) is an opportunistic infection that can occur among patients infected with human immunodeficiency virus type 1 (HIV-1) in areas where both infections are endemic. Highly active antiretroviral therapy has decreased the incidence of VL in southern Europe among HIV-1-infected patients, but VL is still observed among patients with low CD4 cell counts, and most coinfected patients receiving highly active antiretroviral therapy experienced relapse, despite initial treatment with liposomal amphotericin B. METHODS: Through long-term monitoring of VL in 10 patients with HIV-1 infection and/or AIDS, we compared parasite strains derived from primary and secondary episodes of VL. All the patients have received many courses of amphotericin B treatment and/or prophylaxis. RESULTS: Through molecular techniques, we have shown that secondary episodes of VL can be attributable to relapse (7 of 10 episodes) or reinfection (3 of 10). We developed an assay to measure amphotericin B susceptibility and found no evidence of decreased susceptibility among strains isolated from patients, some of whom were infected with the same isolate for up to 10 years. CONCLUSIONS: This apparent absence of resistance, as determined by in vitro susceptibility testing, has important consequences and suggests that amphotericin B will remain a useful drug of choice against VL, even after repetitive treatments or prophylactic use.
BACKGROUND:Visceral leishmaniasis (VL) is an opportunistic infection that can occur among patients infected with human immunodeficiency virus type 1 (HIV-1) in areas where both infections are endemic. Highly active antiretroviral therapy has decreased the incidence of VL in southern Europe among HIV-1-infectedpatients, but VL is still observed among patients with low CD4 cell counts, and most coinfectedpatients receiving highly active antiretroviral therapy experienced relapse, despite initial treatment with liposomal amphotericin B. METHODS: Through long-term monitoring of VL in 10 patients with HIV-1 infection and/or AIDS, we compared parasite strains derived from primary and secondary episodes of VL. All the patients have received many courses of amphotericin B treatment and/or prophylaxis. RESULTS: Through molecular techniques, we have shown that secondary episodes of VL can be attributable to relapse (7 of 10 episodes) or reinfection (3 of 10). We developed an assay to measure amphotericin B susceptibility and found no evidence of decreased susceptibility among strains isolated from patients, some of whom were infected with the same isolate for up to 10 years. CONCLUSIONS: This apparent absence of resistance, as determined by in vitro susceptibility testing, has important consequences and suggests that amphotericin B will remain a useful drug of choice against VL, even after repetitive treatments or prophylactic use.
Authors: Élodie Gazanion; Christopher Fernández-Prada; Barbara Papadopoulou; Philippe Leprohon; Marc Ouellette Journal: Proc Natl Acad Sci U S A Date: 2016-05-09 Impact factor: 11.205
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Authors: Michel Muálem de Moraes Alves; Lucas Moreira Brito; Adriana Cunha Souza; Bárbara Cristina Silva Holanda Queiroz; Thaynara Parente de Carvalho; Joilson Ferreira Batista; Jéssica Sara de Sousa Macêdo Oliveira; Ivete Lopes de Mendonça; Silvéria Regina de Sousa Lira; Mariana Helena Chaves; Juan Carlos Ramos Gonçalves; Sabrina Maria Portela Carneiro; Daniel Dias Rufino Arcanjo; Fernando Aécio de Amorim Carvalho Journal: Naunyn Schmiedebergs Arch Pharmacol Date: 2017-06-22 Impact factor: 3.000
Authors: Michel Muálem de Moraes Alves; Daniel Dias Rufino Arcanjo; Kayo Alves Figueiredo; Jéssica Sara de Sousa Macêdo Oliveira; Felipe José Costa Viana; Elvilene de Sousa Coelho; Glaucia Lais Nunes Lopes; Juan Carlos Ramos Gonçalves; André Luís Menezes Carvalho; Márcia Dos Santos Rizzo; Mariana Helena Chaves; Ivete Lopes de Mendonça; Fernando Aécio de Amorim Carvalho Journal: Antimicrob Agents Chemother Date: 2020-11-17 Impact factor: 5.191