Profile of Thomas E. Wellems.
نویسنده
چکیده
M alaria parasites can hijack red blood cells and escape immune defenses, producing a disease that causes tremendous rates of childhood mortality and disability, especially in Africa. Many medicines developed against malaria have lost efficacy, because the parasites evolve and gain resistance. Thomas E. Wellems, chief of the Laboratory of Malaria and Vector Research in the Division of Intramural Research, National Institutes of Allergy and Infectious Disease (Bethesda, MD), attacks malaria from the laboratory and the field. A researcher and physician, Wellems, who was elected to the National Academy of Sciences in 2007, has not only discovered secrets of Plasmodium falciparum’s ever-changing surface proteins and pinpointed the gene for resistance against the antimalarial drug chloroquine, he has fostered diagnosis and treatment in some of the most affected regions of the world. In his Inaugural Article published in a previous issue of PNAS, Wellems and colleagues show how certain mutations in the chloroquineresistance gene can combine with mutations in another gene for multiple drug resistance to protect malaria parasites against a related antimalarial drug, amodiaquine (1). Parasites with resistance to both amodiaquine and chloroquine blanket the Amazon region of South America, and Wellems worries that Africa may soon find itself in a similar bind.
منابع مشابه
Report of WHO/TDR Scientific Working Group on the Utilization of Genomic Information for Tropical Disease Drug and Vaccine Discovery
s of talks ......................................................................................................................................... 29 Hamilton O. Smith............................................................................................................................ 31 Daniel Lawson .........................................................................................
متن کاملPlasmodium chloroquine resistance and the search for a replacement antimalarial drug.
Genetic and biochemical research is providing new information on the mechanism of chloroquine resistance. Drug discovery initiatives are finding new leads that have favorable pharmaceutical properties and efficacy against chloroquine-resistant malaria.
متن کاملComplex Polymorphisms in an ∼330 kDa Protein Are Linked to Chloroquine-Resistant P. falciparum in Southeast Asia and Africa
The finding that chloroquine resistance can be partially reversed by verapamil, an inhibitor of P glycoprotein–mediated transport in multiple drug-resistant (mdr) mammalian tumor lines, led to
متن کاملA silenced Plasmodium falciparum var promoter can be activated in vivo through spontaneous deletion of a silencing element in the intron.
Introns of Plasmodium falciparum var genes act as transcriptional silencing elements that help control antigenic variations. In transfected episomes, intron silencing of a drug-selectable marker under var promoter control is reversed by the spontaneous deletion of key intron regions. The resulting promoter activation does not affect the transcription of chromosomal var genes.
متن کاملThe Human Genes for GM - CSF and IL 3 Are Closely Linked in Tandem on Chromosome
As demonstrated by long-range mapping of restriction endonuclease recognition sequences and genomic cloning. we found that the human genes encoding interleukin 3 (II 3) and granulocyte/macrophage colony-stimulating factor (GM-CSF) are tandemly arrayed on the long arm of chromosome 5. separated by 9 kilobases (kb) of DNA. This close physical linkage of genes with similar structure and biologic f...
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عنوان ژورنال:
- Proceedings of the National Academy of Sciences of the United States of America
دوره 107 31 شماره
صفحات -
تاریخ انتشار 2010