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1.
J Investig Med High Impact Case Rep ; 11: 23247096231165739, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37052123

RESUMO

Mpox was an emerging outbreak in California in 2022, primarily in major metropolitan areas, as part of the global mpox outbreak declared by World Health Organization in July 2022. Community hospitals outside of major metropolitan areas have seen fewer cases to date, so they may be less equipped to diagnose and treat patients with mpox. They may have limited public health resources commensurate with the area's population density. Mpox may also be superimposed on ongoing local outbreaks of other sexually transmitted infections. We present a case of a person with HIV who contracted mpox and also developed secondary syphilis. Early detection can be beneficial for prompt treatment, decreased burden of disease for the individual, and prevention of further spread of the infection.


Assuntos
Infecções por HIV , Mpox , Sífilis , Humanos , Hospitais Comunitários , Sífilis/complicações , Sífilis/diagnóstico , Infecções por HIV/complicações
2.
Antimicrob Agents Chemother ; 59(6): 3156-67, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25779582

RESUMO

Artemisinin derivatives are used in combination with other antimalarial drugs for treatment of multidrug-resistant malaria worldwide. Clinical resistance to artemisinin recently emerged in southeast Asia, yet in vitro phenotypes for discerning mechanism(s) of resistance remain elusive. Here, we describe novel phenotypic resistance traits expressed by artemisinin-resistant Plasmodium falciparum. The resistant parasites exhibit altered patterns of development that result in reduced exposure to drug at the most susceptible stage of development in erythrocytes (trophozoites) and increased exposure in the most resistant stage (rings). In addition, a novel in vitro delayed clearance assay (DCA) that assesses drug effects on asexual stages was found to correlate with parasite clearance half-life in vivo as well as with mutations in the Kelch domain gene associated with resistance (Pf3D7_1343700). Importantly, all of the resistance phenotypes were stable in cloned parasites for more than 2 years without drug pressure. The results demonstrate artemisinin-resistant P. falciparum has evolved a novel mechanism of phenotypic resistance to artemisinin drugs linked to abnormal cell cycle regulation. These results offer insights into a novel mechanism of drug resistance in P. falciparum and new tools for monitoring the spread of artemisinin resistance.


Assuntos
Antiprotozoários/farmacologia , Artemisininas/farmacologia , Eritrócitos/parasitologia , Plasmodium falciparum/efeitos dos fármacos , Células Cultivadas , Resistência a Medicamentos , Humanos , Hipoxantina/farmacologia , Testes de Sensibilidade Parasitária , Plasmodium falciparum/patogenicidade , Polimorfismo de Nucleotídeo Único
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