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Controlled Human Malaria Infection with Graded Numbers of Plasmodium falciparum NF135.C10- or NF166.C8-Infected Mosquitoes
Controlled human malaria infections (CHMIs) with Plasmodium falciparum (Pf) parasites are well established. Exposure to five Pf (NF54)-infected Anopheles mosquitoes results in 100% infection rates in malaria-naïve volunteers. Recently Pf clones NF135.C10 and NF166.C8 were generated for application i...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The American Society of Tropical Medicine and Hygiene
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6169176/ https://www.ncbi.nlm.nih.gov/pubmed/30014816 http://dx.doi.org/10.4269/ajtmh.18-0194 |
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author | Langenberg, Marijke C. C. Wammes, Linda J. McCall, Matthew B. B. Bijker, Else M. van Gemert, Geert-Jan Graumans, Wouter van de Vegte-Bolmer, Marga G. Teelen, Karina Hermsen, Cornelis C. Koelewijn, Rob van Hellemond, Jaap J. van Genderen, Perry J. J. Sauerwein, Robert W. |
author_facet | Langenberg, Marijke C. C. Wammes, Linda J. McCall, Matthew B. B. Bijker, Else M. van Gemert, Geert-Jan Graumans, Wouter van de Vegte-Bolmer, Marga G. Teelen, Karina Hermsen, Cornelis C. Koelewijn, Rob van Hellemond, Jaap J. van Genderen, Perry J. J. Sauerwein, Robert W. |
author_sort | Langenberg, Marijke C. C. |
collection | PubMed |
description | Controlled human malaria infections (CHMIs) with Plasmodium falciparum (Pf) parasites are well established. Exposure to five Pf (NF54)-infected Anopheles mosquitoes results in 100% infection rates in malaria-naïve volunteers. Recently Pf clones NF135.C10 and NF166.C8 were generated for application in CHMIs. Here, we tested the clinical infection rates of these clones, using graded numbers of Pf-infected mosquitoes. In a double-blind randomized trial, we exposed 24 malaria-naïve volunteers to bites from one, two, or five mosquitoes infected with NF135.C10 or NF166.C8. The primary endpoint was parasitemia by quantitative polymerase chain reaction. For both strains, bites by five infected mosquitoes resulted in parasitemia in 4/4 volunteers; 3/4 volunteers developed parasitemia after exposure to one or two infected mosquitoes infected with either clone. The prepatent period was 7.25 ± 4.0 days (median ± range). There were no serious adverse events and comparable clinical symptoms between all groups. These data confirm the eligibility of NF135.C10 and NF166.C8 for use in CHMI studies. |
format | Online Article Text |
id | pubmed-6169176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The American Society of Tropical Medicine and Hygiene |
record_format | MEDLINE/PubMed |
spelling | pubmed-61691762018-10-10 Controlled Human Malaria Infection with Graded Numbers of Plasmodium falciparum NF135.C10- or NF166.C8-Infected Mosquitoes Langenberg, Marijke C. C. Wammes, Linda J. McCall, Matthew B. B. Bijker, Else M. van Gemert, Geert-Jan Graumans, Wouter van de Vegte-Bolmer, Marga G. Teelen, Karina Hermsen, Cornelis C. Koelewijn, Rob van Hellemond, Jaap J. van Genderen, Perry J. J. Sauerwein, Robert W. Am J Trop Med Hyg Articles Controlled human malaria infections (CHMIs) with Plasmodium falciparum (Pf) parasites are well established. Exposure to five Pf (NF54)-infected Anopheles mosquitoes results in 100% infection rates in malaria-naïve volunteers. Recently Pf clones NF135.C10 and NF166.C8 were generated for application in CHMIs. Here, we tested the clinical infection rates of these clones, using graded numbers of Pf-infected mosquitoes. In a double-blind randomized trial, we exposed 24 malaria-naïve volunteers to bites from one, two, or five mosquitoes infected with NF135.C10 or NF166.C8. The primary endpoint was parasitemia by quantitative polymerase chain reaction. For both strains, bites by five infected mosquitoes resulted in parasitemia in 4/4 volunteers; 3/4 volunteers developed parasitemia after exposure to one or two infected mosquitoes infected with either clone. The prepatent period was 7.25 ± 4.0 days (median ± range). There were no serious adverse events and comparable clinical symptoms between all groups. These data confirm the eligibility of NF135.C10 and NF166.C8 for use in CHMI studies. The American Society of Tropical Medicine and Hygiene 2018-09 2018-07-16 /pmc/articles/PMC6169176/ /pubmed/30014816 http://dx.doi.org/10.4269/ajtmh.18-0194 Text en © The American Society of Tropical Medicine and Hygiene This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Articles Langenberg, Marijke C. C. Wammes, Linda J. McCall, Matthew B. B. Bijker, Else M. van Gemert, Geert-Jan Graumans, Wouter van de Vegte-Bolmer, Marga G. Teelen, Karina Hermsen, Cornelis C. Koelewijn, Rob van Hellemond, Jaap J. van Genderen, Perry J. J. Sauerwein, Robert W. Controlled Human Malaria Infection with Graded Numbers of Plasmodium falciparum NF135.C10- or NF166.C8-Infected Mosquitoes |
title | Controlled Human Malaria Infection with Graded Numbers of Plasmodium falciparum NF135.C10- or NF166.C8-Infected Mosquitoes |
title_full | Controlled Human Malaria Infection with Graded Numbers of Plasmodium falciparum NF135.C10- or NF166.C8-Infected Mosquitoes |
title_fullStr | Controlled Human Malaria Infection with Graded Numbers of Plasmodium falciparum NF135.C10- or NF166.C8-Infected Mosquitoes |
title_full_unstemmed | Controlled Human Malaria Infection with Graded Numbers of Plasmodium falciparum NF135.C10- or NF166.C8-Infected Mosquitoes |
title_short | Controlled Human Malaria Infection with Graded Numbers of Plasmodium falciparum NF135.C10- or NF166.C8-Infected Mosquitoes |
title_sort | controlled human malaria infection with graded numbers of plasmodium falciparum nf135.c10- or nf166.c8-infected mosquitoes |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6169176/ https://www.ncbi.nlm.nih.gov/pubmed/30014816 http://dx.doi.org/10.4269/ajtmh.18-0194 |
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