| Literature DB >> 30201816 |
Ana Gomes1, Ricardo Ferraz1,2, Lauren Ficker3, Margaret S Collins3, Cristina Prudêncio2,4, Melanie T Cushion3, Cátia Teixeira1, Paula Gomes5.
Abstract
The impact of Pneumocystis pneumonia (PcP) on morbidity and mortality remains substantial for immunocompromised individuals, including those afflicted by HIV infection, organ transplantation, cancer, autoimmune diseases, or subject to chemotherapy or corticosteroid-based therapies. Previous work from our group has shown that repurposing antimalarial compounds for PcP holds promise for treatment of this opportunistic infection. Following our previous discovery of chloroquine analogues with dual-stage antimalarial action both in vitro and in vivo, we now report the potent action of these compounds on Pneumocystis carinii in vitro Identification of chloroquine analogues as anti-PcP leads is an unprecedented finding.Entities:
Keywords: Pneumocystis; chloroquine; cinnamic acids; immunosuppressed; lung infection; malaria; pneumonia; primaquine
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Year: 2018 PMID: 30201816 PMCID: PMC6201078 DOI: 10.1128/AAC.00983-18
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191