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Esperanza Herreros

Researcher at GlaxoSmithKline

Publications -  45
Citations -  2178

Esperanza Herreros is an academic researcher from GlaxoSmithKline. The author has contributed to research in topics: Plasmodium falciparum & Gametocyte. The author has an hindex of 22, co-authored 45 publications receiving 1928 citations. Previous affiliations of Esperanza Herreros include Medicines for Malaria Venture.

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Quinolone-3-Diarylethers: A New Class of Antimalarial Drug

TL;DR: ELQ-300, a 4(1H)-quinolone-3-diarylether, which targets the liver and blood stages, including the forms that are crucial to disease transmission (gametocytes, zygotes, and ookinetes), has potential as a new drug for the treatment, prevention, and, ultimately, eradication of human malaria.
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Activity of clinically relevant antimalarial drugs on Plasmodium falciparum mature gametocytes in an ATP bioluminescence “transmission blocking”assay

TL;DR: An efficient method to produce and purify mature gametocytes in vitro and an assay to determine the activity of antimalarial drugs based on the intracellular ATP content of purified stage IV–Vgametocytes after 48 h of drug exposure in 96/384-well microplates are designed.
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Male and Female Plasmodium falciparum Mature Gametocytes Show Different Responses to Antimalarial Drugs

TL;DR: These findings show firstly that the antimalarial responses of male and female gametocytes differ and secondly that the mature male gametocyte should be considered a more vulnerable target than the femalegametocyte for transmission-blocking drugs.
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A murine model of falciparum-malaria by in vivo selection of competent strains in non-myelodepleted mice engrafted with human erythrocytes.

TL;DR: Using this model, a reproducible assay of antimalarial activity useful for drug discovery is implemented and validated and demonstrates that P. falciparum contains clones able to grow reproducibly in mice engrafted with human erythrocytes without the use of myeloablative methods.
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UCT943, a Next-Generation Plasmodium falciparum PI4K Inhibitor Preclinical Candidate for the Treatment of Malaria.

TL;DR: UCT943, based on the combined preclinical data, has the potential to form part of a single-exposure radical cure and prophylaxis (SERCaP) to treat, prevent, and block the transmission of malaria.