Long-term protection against malaria after experimental sporozoite inoculation: an open-label follow-up study

Summary Background We have shown that immunity to infection with Plasmodium falciparum can be induced experimentally in malaria-naive volunteers through immunisation by bites of infected mosquitoes while simultaneously preventing disease with chloroquine prophylaxis. This immunity was associated wit...

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Veröffentlicht in:The Lancet (British edition) 2011-05, Vol.377 (9779), p.1770-1776
Hauptverfasser: Roestenberg, Meta, MD, Teirlinck, Anne C, MSc, McCall, Matthew BB, MD, Teelen, Karina, BSc, Makamdop, Krystelle Nganou, MSc, Wiersma, Jorien, ADN, Arens, Theo, BSc, Beckers, Pieter, PhD, van Gemert, GeertJan, BSc, van de Vegte-Bolmer, Marga, BSc, van der Ven, André JAM, Prof, Luty, Adrian JF, PhD, Hermsen, Cornelus C, PhD, Sauerwein, Robert W, Prof
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container_end_page 1776
container_issue 9779
container_start_page 1770
container_title The Lancet (British edition)
container_volume 377
creator Roestenberg, Meta, MD
Teirlinck, Anne C, MSc
McCall, Matthew BB, MD
Teelen, Karina, BSc
Makamdop, Krystelle Nganou, MSc
Wiersma, Jorien, ADN
Arens, Theo, BSc
Beckers, Pieter, PhD
van Gemert, GeertJan, BSc
van de Vegte-Bolmer, Marga, BSc
van der Ven, André JAM, Prof
Luty, Adrian JF, PhD
Hermsen, Cornelus C, PhD
Sauerwein, Robert W, Prof
description Summary Background We have shown that immunity to infection with Plasmodium falciparum can be induced experimentally in malaria-naive volunteers through immunisation by bites of infected mosquitoes while simultaneously preventing disease with chloroquine prophylaxis. This immunity was associated with parasite-specific production of interferon γ and interleukin 2 by pluripotent effector memory cells in vitro. We aim to explore the persistence of protection and immune responses in the same volunteers. Methods In an open-label study at the Radboud University Nijmegen Medical Centre (Nijmegen, Netherlands), from November to December, 2009, we rechallenged previously immune volunteers (28 months after immunisation) with the bites of five mosquitoes infected with P falciparum . Newly recruited malaria-naive volunteers served as infection controls. Our primary outcome was the detection of blood-stage parasitaemia by microscopy. We assessed the kinetics of parasitaemia with real-time quantitative PCR (rtPCR) and recorded clinical signs and symptoms. In-vitro production of interferon γ and interleukin 2 by effector memory T cells was studied after stimulation with sporozoites and red blood cells infected with P falciparum . Differences in cellular immune responses between the study groups were assessed with the Mann-Whitney test. This study is registered with ClinicalTrials.gov , number NCT00757887. Findings Four of six immune volunteers were microscopically negative after rechallenge. rtPCR-based detection of blood-stage parasites in these individuals was negative throughout follow-up. Patent parasitaemia was delayed in the remaining two immunised volunteers. In-vitro assays showed the long-term persistence of parasite-specific pluripotent effector memory T-cell responses in protected volunteers. The four protected volunteers reported several mild to moderate adverse events, of which the most commonly reported symptom was headache (one to three episodes per volunteer). The two patients with delayed patency had adverse events similar to those in the control group. Interpretation Artificially induced immunity lasts longer than generally recorded after natural exposure; providing a new avenue of research into the mechanisms of malaria immunity. Funding Dioraphte Foundation.
doi_str_mv 10.1016/S0140-6736(11)60360-7
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This immunity was associated with parasite-specific production of interferon γ and interleukin 2 by pluripotent effector memory cells in vitro. We aim to explore the persistence of protection and immune responses in the same volunteers. Methods In an open-label study at the Radboud University Nijmegen Medical Centre (Nijmegen, Netherlands), from November to December, 2009, we rechallenged previously immune volunteers (28 months after immunisation) with the bites of five mosquitoes infected with P falciparum . Newly recruited malaria-naive volunteers served as infection controls. Our primary outcome was the detection of blood-stage parasitaemia by microscopy. We assessed the kinetics of parasitaemia with real-time quantitative PCR (rtPCR) and recorded clinical signs and symptoms. In-vitro production of interferon γ and interleukin 2 by effector memory T cells was studied after stimulation with sporozoites and red blood cells infected with P falciparum . Differences in cellular immune responses between the study groups were assessed with the Mann-Whitney test. This study is registered with ClinicalTrials.gov , number NCT00757887. Findings Four of six immune volunteers were microscopically negative after rechallenge. rtPCR-based detection of blood-stage parasites in these individuals was negative throughout follow-up. Patent parasitaemia was delayed in the remaining two immunised volunteers. In-vitro assays showed the long-term persistence of parasite-specific pluripotent effector memory T-cell responses in protected volunteers. The four protected volunteers reported several mild to moderate adverse events, of which the most commonly reported symptom was headache (one to three episodes per volunteer). The two patients with delayed patency had adverse events similar to those in the control group. Interpretation Artificially induced immunity lasts longer than generally recorded after natural exposure; providing a new avenue of research into the mechanisms of malaria immunity. Funding Dioraphte Foundation.</description><identifier>ISSN: 0140-6736</identifier><identifier>EISSN: 1474-547X</identifier><identifier>DOI: 10.1016/S0140-6736(11)60360-7</identifier><identifier>PMID: 21514658</identifier><identifier>CODEN: LANCAO</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Adaptive Immunity - immunology ; Adult ; Antibody Specificity - immunology ; Antimalarials - administration &amp; dosage ; Antimalarials - adverse effects ; Aquatic insects ; Biological and medical sciences ; cell-mediated immunity ; chloroquine ; Chloroquine - administration &amp; dosage ; Clinical medicine ; Culicidae ; disease control ; erythrocytes ; Female ; General aspects ; headache ; Hepatitis ; Human protozoal diseases ; Human subjects ; Humans ; immune response ; Immunization ; Immunization - adverse effects ; Immunization - methods ; Immunologic Memory - immunology ; Infectious diseases ; interferon-gamma ; Interferon-gamma - blood ; interleukin-2 ; Interleukin-2 - blood ; Internal Medicine ; Malaria ; Malaria, Falciparum - immunology ; Malaria, Falciparum - prevention &amp; control ; Male ; Medical sciences ; microscopy ; Mosquitoes ; Netherlands ; parasitemia ; Parasites ; Parasitic diseases ; patients ; Plasmodium falciparum ; Plasmodium falciparum - immunology ; Prophylaxis ; Protozoal diseases ; quantitative polymerase chain reaction ; Reverse Transcriptase Polymerase Chain Reaction ; sporozoites ; Sporozoites - immunology ; T-lymphocytes ; T-Lymphocytes - immunology ; Vector-borne diseases ; volunteers ; Young Adult</subject><ispartof>The Lancet (British edition), 2011-05, Vol.377 (9779), p.1770-1776</ispartof><rights>Elsevier Ltd</rights><rights>2011 Elsevier Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 Elsevier Ltd. All rights reserved.</rights><rights>Copyright Elsevier Limited May 21-May 27, 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c598t-b529653f693cae80147c7557defb2d20592dc4bea6a9bcc31a60392a8510f02d3</citedby><cites>FETCH-LOGICAL-c598t-b529653f693cae80147c7557defb2d20592dc4bea6a9bcc31a60392a8510f02d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/868670494?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976,64364,64366,64368,72218</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=24185206$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21514658$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Roestenberg, Meta, MD</creatorcontrib><creatorcontrib>Teirlinck, Anne C, MSc</creatorcontrib><creatorcontrib>McCall, Matthew BB, MD</creatorcontrib><creatorcontrib>Teelen, Karina, BSc</creatorcontrib><creatorcontrib>Makamdop, Krystelle Nganou, MSc</creatorcontrib><creatorcontrib>Wiersma, Jorien, ADN</creatorcontrib><creatorcontrib>Arens, Theo, BSc</creatorcontrib><creatorcontrib>Beckers, Pieter, PhD</creatorcontrib><creatorcontrib>van Gemert, GeertJan, BSc</creatorcontrib><creatorcontrib>van de Vegte-Bolmer, Marga, BSc</creatorcontrib><creatorcontrib>van der Ven, André JAM, Prof</creatorcontrib><creatorcontrib>Luty, Adrian JF, PhD</creatorcontrib><creatorcontrib>Hermsen, Cornelus C, PhD</creatorcontrib><creatorcontrib>Sauerwein, Robert W, Prof</creatorcontrib><title>Long-term protection against malaria after experimental sporozoite inoculation: an open-label follow-up study</title><title>The Lancet (British edition)</title><addtitle>Lancet</addtitle><description>Summary Background We have shown that immunity to infection with Plasmodium falciparum can be induced experimentally in malaria-naive volunteers through immunisation by bites of infected mosquitoes while simultaneously preventing disease with chloroquine prophylaxis. This immunity was associated with parasite-specific production of interferon γ and interleukin 2 by pluripotent effector memory cells in vitro. We aim to explore the persistence of protection and immune responses in the same volunteers. Methods In an open-label study at the Radboud University Nijmegen Medical Centre (Nijmegen, Netherlands), from November to December, 2009, we rechallenged previously immune volunteers (28 months after immunisation) with the bites of five mosquitoes infected with P falciparum . Newly recruited malaria-naive volunteers served as infection controls. Our primary outcome was the detection of blood-stage parasitaemia by microscopy. We assessed the kinetics of parasitaemia with real-time quantitative PCR (rtPCR) and recorded clinical signs and symptoms. In-vitro production of interferon γ and interleukin 2 by effector memory T cells was studied after stimulation with sporozoites and red blood cells infected with P falciparum . Differences in cellular immune responses between the study groups were assessed with the Mann-Whitney test. This study is registered with ClinicalTrials.gov , number NCT00757887. Findings Four of six immune volunteers were microscopically negative after rechallenge. rtPCR-based detection of blood-stage parasites in these individuals was negative throughout follow-up. Patent parasitaemia was delayed in the remaining two immunised volunteers. In-vitro assays showed the long-term persistence of parasite-specific pluripotent effector memory T-cell responses in protected volunteers. The four protected volunteers reported several mild to moderate adverse events, of which the most commonly reported symptom was headache (one to three episodes per volunteer). The two patients with delayed patency had adverse events similar to those in the control group. Interpretation Artificially induced immunity lasts longer than generally recorded after natural exposure; providing a new avenue of research into the mechanisms of malaria immunity. Funding Dioraphte Foundation.</description><subject>Adaptive Immunity - immunology</subject><subject>Adult</subject><subject>Antibody Specificity - immunology</subject><subject>Antimalarials - administration &amp; dosage</subject><subject>Antimalarials - adverse effects</subject><subject>Aquatic insects</subject><subject>Biological and medical sciences</subject><subject>cell-mediated immunity</subject><subject>chloroquine</subject><subject>Chloroquine - administration &amp; dosage</subject><subject>Clinical medicine</subject><subject>Culicidae</subject><subject>disease control</subject><subject>erythrocytes</subject><subject>Female</subject><subject>General aspects</subject><subject>headache</subject><subject>Hepatitis</subject><subject>Human protozoal diseases</subject><subject>Human subjects</subject><subject>Humans</subject><subject>immune response</subject><subject>Immunization</subject><subject>Immunization - adverse effects</subject><subject>Immunization - methods</subject><subject>Immunologic Memory - immunology</subject><subject>Infectious diseases</subject><subject>interferon-gamma</subject><subject>Interferon-gamma - blood</subject><subject>interleukin-2</subject><subject>Interleukin-2 - blood</subject><subject>Internal Medicine</subject><subject>Malaria</subject><subject>Malaria, Falciparum - immunology</subject><subject>Malaria, Falciparum - prevention &amp; 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Fisheries Abstracts (ASFA) 1: Biological Sciences &amp; Living Resources</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) 3: Aquatic Pollution &amp; Environmental Quality</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) Professional</collection><jtitle>The Lancet (British edition)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Roestenberg, Meta, MD</au><au>Teirlinck, Anne C, MSc</au><au>McCall, Matthew BB, MD</au><au>Teelen, Karina, BSc</au><au>Makamdop, Krystelle Nganou, MSc</au><au>Wiersma, Jorien, ADN</au><au>Arens, Theo, BSc</au><au>Beckers, Pieter, PhD</au><au>van Gemert, GeertJan, BSc</au><au>van de Vegte-Bolmer, Marga, BSc</au><au>van der Ven, André JAM, Prof</au><au>Luty, Adrian JF, PhD</au><au>Hermsen, Cornelus C, PhD</au><au>Sauerwein, Robert W, Prof</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-term protection against malaria after experimental sporozoite inoculation: an open-label follow-up study</atitle><jtitle>The Lancet (British edition)</jtitle><addtitle>Lancet</addtitle><date>2011-05-21</date><risdate>2011</risdate><volume>377</volume><issue>9779</issue><spage>1770</spage><epage>1776</epage><pages>1770-1776</pages><issn>0140-6736</issn><eissn>1474-547X</eissn><coden>LANCAO</coden><abstract>Summary Background We have shown that immunity to infection with Plasmodium falciparum can be induced experimentally in malaria-naive volunteers through immunisation by bites of infected mosquitoes while simultaneously preventing disease with chloroquine prophylaxis. This immunity was associated with parasite-specific production of interferon γ and interleukin 2 by pluripotent effector memory cells in vitro. We aim to explore the persistence of protection and immune responses in the same volunteers. Methods In an open-label study at the Radboud University Nijmegen Medical Centre (Nijmegen, Netherlands), from November to December, 2009, we rechallenged previously immune volunteers (28 months after immunisation) with the bites of five mosquitoes infected with P falciparum . Newly recruited malaria-naive volunteers served as infection controls. Our primary outcome was the detection of blood-stage parasitaemia by microscopy. We assessed the kinetics of parasitaemia with real-time quantitative PCR (rtPCR) and recorded clinical signs and symptoms. In-vitro production of interferon γ and interleukin 2 by effector memory T cells was studied after stimulation with sporozoites and red blood cells infected with P falciparum . Differences in cellular immune responses between the study groups were assessed with the Mann-Whitney test. This study is registered with ClinicalTrials.gov , number NCT00757887. Findings Four of six immune volunteers were microscopically negative after rechallenge. rtPCR-based detection of blood-stage parasites in these individuals was negative throughout follow-up. Patent parasitaemia was delayed in the remaining two immunised volunteers. In-vitro assays showed the long-term persistence of parasite-specific pluripotent effector memory T-cell responses in protected volunteers. The four protected volunteers reported several mild to moderate adverse events, of which the most commonly reported symptom was headache (one to three episodes per volunteer). The two patients with delayed patency had adverse events similar to those in the control group. Interpretation Artificially induced immunity lasts longer than generally recorded after natural exposure; providing a new avenue of research into the mechanisms of malaria immunity. Funding Dioraphte Foundation.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>21514658</pmid><doi>10.1016/S0140-6736(11)60360-7</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0140-6736
ispartof The Lancet (British edition), 2011-05, Vol.377 (9779), p.1770-1776
issn 0140-6736
1474-547X
language eng
recordid cdi_proquest_miscellaneous_872138561
source MEDLINE; Elsevier ScienceDirect Journals; ProQuest Central UK/Ireland
subjects Adaptive Immunity - immunology
Adult
Antibody Specificity - immunology
Antimalarials - administration & dosage
Antimalarials - adverse effects
Aquatic insects
Biological and medical sciences
cell-mediated immunity
chloroquine
Chloroquine - administration & dosage
Clinical medicine
Culicidae
disease control
erythrocytes
Female
General aspects
headache
Hepatitis
Human protozoal diseases
Human subjects
Humans
immune response
Immunization
Immunization - adverse effects
Immunization - methods
Immunologic Memory - immunology
Infectious diseases
interferon-gamma
Interferon-gamma - blood
interleukin-2
Interleukin-2 - blood
Internal Medicine
Malaria
Malaria, Falciparum - immunology
Malaria, Falciparum - prevention & control
Male
Medical sciences
microscopy
Mosquitoes
Netherlands
parasitemia
Parasites
Parasitic diseases
patients
Plasmodium falciparum
Plasmodium falciparum - immunology
Prophylaxis
Protozoal diseases
quantitative polymerase chain reaction
Reverse Transcriptase Polymerase Chain Reaction
sporozoites
Sporozoites - immunology
T-lymphocytes
T-Lymphocytes - immunology
Vector-borne diseases
volunteers
Young Adult
title Long-term protection against malaria after experimental sporozoite inoculation: an open-label follow-up study
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