Antibody profiles to plasmodium merozoite surface protein-1 in Cambodian adults during an active surveillance cohort with nested treatment study

In addition to evidence for a protective role of antibodies to the malaria blood stage antigen merozoite surface protein 1 (MSP1), MSP1 antibodies are also considered as a marker of past malaria exposure in sero-epidemiological studies. In order to better assess the potential use of MSP1 serology in...

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Veröffentlicht in:Malaria journal 2016-01, Vol.15 (18), p.17-17, Article 17
Hauptverfasser: Spring, Michele D, Pichyangkul, Sathit, Lon, Chanthap, Gosi, Panita, Yongvanichit, Kosol, Srichairatanakul, Utaiwan, Limsalakpeth, Amporn, Chaisatit, Chaiyaporn, Chann, Soklyda, Sriwichai, Sabaithip, Auayapon, Montida, Chaorattanakawee, Suwanna, Dutta, Sheetij, Prom, Satharath, Meng Chour, Char, Walsh, Douglas S, Angov, Evelina, Saunders, David L
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container_issue 18
container_start_page 17
container_title Malaria journal
container_volume 15
creator Spring, Michele D
Pichyangkul, Sathit
Lon, Chanthap
Gosi, Panita
Yongvanichit, Kosol
Srichairatanakul, Utaiwan
Limsalakpeth, Amporn
Chaisatit, Chaiyaporn
Chann, Soklyda
Sriwichai, Sabaithip
Auayapon, Montida
Chaorattanakawee, Suwanna
Dutta, Sheetij
Prom, Satharath
Meng Chour, Char
Walsh, Douglas S
Angov, Evelina
Saunders, David L
description In addition to evidence for a protective role of antibodies to the malaria blood stage antigen merozoite surface protein 1 (MSP1), MSP1 antibodies are also considered as a marker of past malaria exposure in sero-epidemiological studies. In order to better assess the potential use of MSP1 serology in malaria chemoprophylaxis trials in endemic areas, an analysis for the prevalence of antibodies to both Plasmodium falciparum and Plasmodium vivax MSP142 in healthy Cambodian adults was conducted at two sites as part of an active, observational cohort evaluating the efficacy of dihydroartemisinin-piperaquine (DP) for uncomplicated malaria (ClinicalTrials.gov identifier NCT01280162). Rates of baseline sero-positivity were high (59 and 73% for PfMSP142 and PvMSP142, respectively), and titers higher in those who lived in a higher transmission area, although there was little correlation in titers between the two species. Those volunteers who subsequently went on to develop malaria had higher baseline MSP142 titers than those who did not for both species. Titers to both antigens remained largely stable over the course of the 4-6 month study, except in those infected with P. falciparum who had multiple recurrences. These findings illuminate the difficulties in using MSP142 serology as either a screening criterion and/or biomarker of exposure in chemoprophylaxis studies. Further work remains to identify useful markers of malarial infection and/or immunity.
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Pichyangkul, Sathit ; Lon, Chanthap ; Gosi, Panita ; Yongvanichit, Kosol ; Srichairatanakul, Utaiwan ; Limsalakpeth, Amporn ; Chaisatit, Chaiyaporn ; Chann, Soklyda ; Sriwichai, Sabaithip ; Auayapon, Montida ; Chaorattanakawee, Suwanna ; Dutta, Sheetij ; Prom, Satharath ; Meng Chour, Char ; Walsh, Douglas S ; Angov, Evelina ; Saunders, David L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c466t-33bde5bfae3a2010cef72cf3e23ee1156c621a1efb9280819979858ad43516fc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adult</topic><topic>Antibodies</topic><topic>Antibodies, Protozoan - immunology</topic><topic>Antigens, Protozoan - immunology</topic><topic>Antimalarials</topic><topic>Artemisinins - therapeutic use</topic><topic>Chemoprevention</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Female</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Malaria</topic><topic>Malaria - drug therapy</topic><topic>Malaria - immunology</topic><topic>Malaria, Falciparum - drug therapy</topic><topic>Malaria, Falciparum - immunology</topic><topic>Male</topic><topic>Merozoite Surface Protein 1 - immunology</topic><topic>Physiological aspects</topic><topic>Plasmodium falciparum - immunology</topic><topic>Plasmodium falciparum - pathogenicity</topic><topic>Plasmodium vivax - immunology</topic><topic>Plasmodium vivax - pathogenicity</topic><topic>Viral antibodies</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Spring, Michele D</creatorcontrib><creatorcontrib>Pichyangkul, Sathit</creatorcontrib><creatorcontrib>Lon, Chanthap</creatorcontrib><creatorcontrib>Gosi, Panita</creatorcontrib><creatorcontrib>Yongvanichit, Kosol</creatorcontrib><creatorcontrib>Srichairatanakul, Utaiwan</creatorcontrib><creatorcontrib>Limsalakpeth, Amporn</creatorcontrib><creatorcontrib>Chaisatit, Chaiyaporn</creatorcontrib><creatorcontrib>Chann, Soklyda</creatorcontrib><creatorcontrib>Sriwichai, Sabaithip</creatorcontrib><creatorcontrib>Auayapon, Montida</creatorcontrib><creatorcontrib>Chaorattanakawee, Suwanna</creatorcontrib><creatorcontrib>Dutta, Sheetij</creatorcontrib><creatorcontrib>Prom, Satharath</creatorcontrib><creatorcontrib>Meng Chour, Char</creatorcontrib><creatorcontrib>Walsh, Douglas S</creatorcontrib><creatorcontrib>Angov, Evelina</creatorcontrib><creatorcontrib>Saunders, David L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Malaria journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Spring, Michele D</au><au>Pichyangkul, Sathit</au><au>Lon, Chanthap</au><au>Gosi, Panita</au><au>Yongvanichit, Kosol</au><au>Srichairatanakul, Utaiwan</au><au>Limsalakpeth, Amporn</au><au>Chaisatit, Chaiyaporn</au><au>Chann, Soklyda</au><au>Sriwichai, Sabaithip</au><au>Auayapon, Montida</au><au>Chaorattanakawee, Suwanna</au><au>Dutta, Sheetij</au><au>Prom, Satharath</au><au>Meng Chour, Char</au><au>Walsh, Douglas S</au><au>Angov, Evelina</au><au>Saunders, David L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antibody profiles to plasmodium merozoite surface protein-1 in Cambodian adults during an active surveillance cohort with nested treatment study</atitle><jtitle>Malaria journal</jtitle><addtitle>Malar J</addtitle><date>2016-01-08</date><risdate>2016</risdate><volume>15</volume><issue>18</issue><spage>17</spage><epage>17</epage><pages>17-17</pages><artnum>17</artnum><issn>1475-2875</issn><eissn>1475-2875</eissn><abstract>In addition to evidence for a protective role of antibodies to the malaria blood stage antigen merozoite surface protein 1 (MSP1), MSP1 antibodies are also considered as a marker of past malaria exposure in sero-epidemiological studies. In order to better assess the potential use of MSP1 serology in malaria chemoprophylaxis trials in endemic areas, an analysis for the prevalence of antibodies to both Plasmodium falciparum and Plasmodium vivax MSP142 in healthy Cambodian adults was conducted at two sites as part of an active, observational cohort evaluating the efficacy of dihydroartemisinin-piperaquine (DP) for uncomplicated malaria (ClinicalTrials.gov identifier NCT01280162). Rates of baseline sero-positivity were high (59 and 73% for PfMSP142 and PvMSP142, respectively), and titers higher in those who lived in a higher transmission area, although there was little correlation in titers between the two species. Those volunteers who subsequently went on to develop malaria had higher baseline MSP142 titers than those who did not for both species. Titers to both antigens remained largely stable over the course of the 4-6 month study, except in those infected with P. falciparum who had multiple recurrences. These findings illuminate the difficulties in using MSP142 serology as either a screening criterion and/or biomarker of exposure in chemoprophylaxis studies. Further work remains to identify useful markers of malarial infection and/or immunity.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>26747132</pmid><doi>10.1186/s12936-015-1058-8</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Antibodies
Antibodies, Protozoan - immunology
Antigens, Protozoan - immunology
Antimalarials
Artemisinins - therapeutic use
Chemoprevention
Enzyme-Linked Immunosorbent Assay
Female
Health aspects
Humans
Malaria
Malaria - drug therapy
Malaria - immunology
Malaria, Falciparum - drug therapy
Malaria, Falciparum - immunology
Male
Merozoite Surface Protein 1 - immunology
Physiological aspects
Plasmodium falciparum - immunology
Plasmodium falciparum - pathogenicity
Plasmodium vivax - immunology
Plasmodium vivax - pathogenicity
Viral antibodies
Young Adult
title Antibody profiles to plasmodium merozoite surface protein-1 in Cambodian adults during an active surveillance cohort with nested treatment study
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