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 |
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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. |
doi_str_mv | 10.1186/s12936-015-1058-8 |
format | Article |
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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.</description><identifier>ISSN: 1475-2875</identifier><identifier>EISSN: 1475-2875</identifier><identifier>DOI: 10.1186/s12936-015-1058-8</identifier><identifier>PMID: 26747132</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>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</subject><ispartof>Malaria journal, 2016-01, Vol.15 (18), p.17-17, Article 17</ispartof><rights>COPYRIGHT 2016 BioMed Central Ltd.</rights><rights>Spring et al. 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c466t-33bde5bfae3a2010cef72cf3e23ee1156c621a1efb9280819979858ad43516fc3</citedby><cites>FETCH-LOGICAL-c466t-33bde5bfae3a2010cef72cf3e23ee1156c621a1efb9280819979858ad43516fc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4706704/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4706704/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,865,886,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26747132$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>Antibody profiles to plasmodium merozoite surface protein-1 in Cambodian adults during an active surveillance cohort with nested treatment study</title><title>Malaria journal</title><addtitle>Malar J</addtitle><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.</description><subject>Adult</subject><subject>Antibodies</subject><subject>Antibodies, Protozoan - immunology</subject><subject>Antigens, Protozoan - immunology</subject><subject>Antimalarials</subject><subject>Artemisinins - therapeutic use</subject><subject>Chemoprevention</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Female</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Malaria</subject><subject>Malaria - drug therapy</subject><subject>Malaria - immunology</subject><subject>Malaria, Falciparum - drug therapy</subject><subject>Malaria, Falciparum - immunology</subject><subject>Male</subject><subject>Merozoite Surface Protein 1 - immunology</subject><subject>Physiological aspects</subject><subject>Plasmodium falciparum - immunology</subject><subject>Plasmodium falciparum - pathogenicity</subject><subject>Plasmodium vivax - immunology</subject><subject>Plasmodium vivax - pathogenicity</subject><subject>Viral antibodies</subject><subject>Young Adult</subject><issn>1475-2875</issn><issn>1475-2875</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptks2KFDEUhQtRnHH0AdxIwI2bGnOTSiW1EZrGPxhwo-uQSt10R6qSNkm1tE_hI1tlj8MMSBYJyfkO95BTVS-BXgOo9m0G1vG2piBqoELV6lF1CY0UNVNSPL53vqie5fydUpBKsqfVBWtlI4Gzy-r3JhTfx-FEDik6P2ImJZLDaPIUBz9PZMIUf0VfkOQ5OWNxFRb0oQbiA9maaaG9CcQM81gyGebkw46sF7b441_siH4cTVhYG_cxFfLTlz0JmAsOpCQ0ZcJQSC7zcHpePXFmzPjidr-qvn14_3X7qb758vHzdnNT26ZtS815P6DonUFuGAVq0UlmHUfGEQFEa1sGBtD1HVNUQdfJTgllhoYLaJ3lV9W7s-9h7icc7DJAMqM-JD-ZdNLReP3wJfi93sWjbiRtJW0Wgze3Bin-mJcsevLZ4hoU45w1yJaqTkAjFunrs3RnRtQ-uLg42lWuN40ALjqQq-H1f1TLGnDyNgZcv-chAGfApphzQnc3PVC9FkSfC6KXgui1IFotzKv7se-If43gfwDq6bob</recordid><startdate>20160108</startdate><enddate>20160108</enddate><creator>Spring, Michele D</creator><creator>Pichyangkul, Sathit</creator><creator>Lon, Chanthap</creator><creator>Gosi, Panita</creator><creator>Yongvanichit, Kosol</creator><creator>Srichairatanakul, Utaiwan</creator><creator>Limsalakpeth, Amporn</creator><creator>Chaisatit, Chaiyaporn</creator><creator>Chann, Soklyda</creator><creator>Sriwichai, Sabaithip</creator><creator>Auayapon, Montida</creator><creator>Chaorattanakawee, Suwanna</creator><creator>Dutta, Sheetij</creator><creator>Prom, Satharath</creator><creator>Meng Chour, Char</creator><creator>Walsh, Douglas S</creator><creator>Angov, Evelina</creator><creator>Saunders, David L</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160108</creationdate><title>Antibody profiles to plasmodium merozoite surface protein-1 in Cambodian adults during an active surveillance cohort with nested treatment study</title><author>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</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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