Controlled Human Malaria Infection with Graded Numbers of Plasmodium falciparum NF135.C10- or NF166.C8-Infected Mosquitoes
Controlled human malaria infections (CHMIs) with ( ) parasites are well established. Exposure to five (NF54)-infected mosquitoes results in 100% infection rates in malaria-naïve volunteers. Recently clones NF135.C10 and NF166.C8 were generated for application in CHMIs. Here, we tested the clinical i...
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Veröffentlicht in: | The American journal of tropical medicine and hygiene 2018-01, Vol.99 (3), p.709-712 |
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creator | 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 |
description | Controlled human malaria infections (CHMIs) with
(
) parasites are well established. Exposure to five
(NF54)-infected
mosquitoes results in 100% infection rates in malaria-naïve volunteers. Recently
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
-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. |
doi_str_mv | 10.4269/ajtmh.18-0194 |
format | Article |
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(
) parasites are well established. Exposure to five
(NF54)-infected
mosquitoes results in 100% infection rates in malaria-naïve volunteers. Recently
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
-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.</description><identifier>ISSN: 0002-9637</identifier><identifier>EISSN: 1476-1645</identifier><identifier>DOI: 10.4269/ajtmh.18-0194</identifier><identifier>PMID: 30014816</identifier><language>eng</language><publisher>United States: Institute of Tropical Medicine</publisher><subject>Erythrocytes ; Infections ; Malaria ; Mosquitoes</subject><ispartof>The American journal of tropical medicine and hygiene, 2018-01, Vol.99 (3), p.709-712</ispartof><rights>Copyright Institute of Tropical Medicine 2018</rights><rights>The American Society of Tropical Medicine and Hygiene 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-ea4203f5245745f3cf9b78034cfc692657390c26d3f11dd841cb142e3b180b203</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6169176/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6169176/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,729,782,786,887,27931,27932,53798,53800</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30014816$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Langenberg, Marijke C C</creatorcontrib><creatorcontrib>Wammes, Linda J</creatorcontrib><creatorcontrib>McCall, Matthew B B</creatorcontrib><creatorcontrib>Bijker, Else M</creatorcontrib><creatorcontrib>van Gemert, Geert-Jan</creatorcontrib><creatorcontrib>Graumans, Wouter</creatorcontrib><creatorcontrib>van de Vegte-Bolmer, Marga G</creatorcontrib><creatorcontrib>Teelen, Karina</creatorcontrib><creatorcontrib>Hermsen, Cornelis C</creatorcontrib><creatorcontrib>Koelewijn, Rob</creatorcontrib><creatorcontrib>van Hellemond, Jaap J</creatorcontrib><creatorcontrib>van Genderen, Perry J J</creatorcontrib><creatorcontrib>Sauerwein, Robert W</creatorcontrib><title>Controlled Human Malaria Infection with Graded Numbers of Plasmodium falciparum NF135.C10- or NF166.C8-Infected Mosquitoes</title><title>The American journal of tropical medicine and hygiene</title><addtitle>Am J Trop Med Hyg</addtitle><description>Controlled human malaria infections (CHMIs) with
(
) parasites are well established. Exposure to five
(NF54)-infected
mosquitoes results in 100% infection rates in malaria-naïve volunteers. Recently
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
-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.</description><subject>Erythrocytes</subject><subject>Infections</subject><subject>Malaria</subject><subject>Mosquitoes</subject><issn>0002-9637</issn><issn>1476-1645</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpdkctv1DAQxi0EokvLkSuKxIWLF49fcS5IKKIPqQ8O9Gw5js16lcRbOwHBX4-XLVXb08zIv_k8nz6E3gFZcyqbT2Y7j5s1KEyg4S_QCngtMUguXqIVIYTiRrL6CL3JeUsIKArwGh2x0nIFcoX-tHGaUxwG11fny2im6soMJgVTXUze2TnEqfoV5k11lkxfmOtl7FzKVfTVt8HkMfZhGStvBht2JpX2-hSYWLdAcBXTfpJy3Sp8UCsCVzHfLWGOLp-gV2Uvu7f39Rjdnn793p7jy5uzi_bLJbYcxIyd4ZQwLygXNReeWd90tSKMW29lQ6WoWUMslT3zAH2vONgOOHWsA0W6snqMPh90d0s3ut66YtgMepfCaNJvHU3QT1-msNE_4k8tQTZQyyLw8V4gxbvF5VmPIVs3DGZyccmakhrKFUrt__rwDN3GJU3FnqYggQjJuCgUPlA2xZyT8w_HANH7VPW_VDUovU-18O8fO3ig_8fI_gJKk5zU</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>Langenberg, Marijke C C</creator><creator>Wammes, Linda J</creator><creator>McCall, Matthew B B</creator><creator>Bijker, Else M</creator><creator>van Gemert, Geert-Jan</creator><creator>Graumans, Wouter</creator><creator>van de Vegte-Bolmer, Marga G</creator><creator>Teelen, Karina</creator><creator>Hermsen, Cornelis C</creator><creator>Koelewijn, Rob</creator><creator>van Hellemond, Jaap J</creator><creator>van Genderen, Perry J J</creator><creator>Sauerwein, Robert W</creator><general>Institute of Tropical Medicine</general><general>The American Society of Tropical Medicine and Hygiene</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20180101</creationdate><title>Controlled Human Malaria Infection with Graded Numbers of Plasmodium falciparum NF135.C10- or NF166.C8-Infected Mosquitoes</title><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></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-ea4203f5245745f3cf9b78034cfc692657390c26d3f11dd841cb142e3b180b203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Erythrocytes</topic><topic>Infections</topic><topic>Malaria</topic><topic>Mosquitoes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Langenberg, Marijke C C</creatorcontrib><creatorcontrib>Wammes, Linda J</creatorcontrib><creatorcontrib>McCall, Matthew B B</creatorcontrib><creatorcontrib>Bijker, Else M</creatorcontrib><creatorcontrib>van Gemert, Geert-Jan</creatorcontrib><creatorcontrib>Graumans, Wouter</creatorcontrib><creatorcontrib>van de Vegte-Bolmer, Marga G</creatorcontrib><creatorcontrib>Teelen, Karina</creatorcontrib><creatorcontrib>Hermsen, Cornelis C</creatorcontrib><creatorcontrib>Koelewijn, Rob</creatorcontrib><creatorcontrib>van Hellemond, Jaap J</creatorcontrib><creatorcontrib>van Genderen, Perry J J</creatorcontrib><creatorcontrib>Sauerwein, Robert W</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The American journal of tropical medicine and hygiene</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Langenberg, Marijke C C</au><au>Wammes, Linda J</au><au>McCall, Matthew B B</au><au>Bijker, Else M</au><au>van Gemert, Geert-Jan</au><au>Graumans, Wouter</au><au>van de Vegte-Bolmer, Marga G</au><au>Teelen, Karina</au><au>Hermsen, Cornelis C</au><au>Koelewijn, Rob</au><au>van Hellemond, Jaap J</au><au>van Genderen, Perry J J</au><au>Sauerwein, Robert W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Controlled Human Malaria Infection with Graded Numbers of Plasmodium falciparum NF135.C10- or NF166.C8-Infected Mosquitoes</atitle><jtitle>The American journal of tropical medicine and hygiene</jtitle><addtitle>Am J Trop Med Hyg</addtitle><date>2018-01-01</date><risdate>2018</risdate><volume>99</volume><issue>3</issue><spage>709</spage><epage>712</epage><pages>709-712</pages><issn>0002-9637</issn><eissn>1476-1645</eissn><abstract>Controlled human malaria infections (CHMIs) with
(
) parasites are well established. Exposure to five
(NF54)-infected
mosquitoes results in 100% infection rates in malaria-naïve volunteers. Recently
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
-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.</abstract><cop>United States</cop><pub>Institute of Tropical Medicine</pub><pmid>30014816</pmid><doi>10.4269/ajtmh.18-0194</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Erythrocytes Infections Malaria Mosquitoes |
title | Controlled Human Malaria Infection with Graded Numbers of Plasmodium falciparum NF135.C10- or NF166.C8-Infected Mosquitoes |
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