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Temporal analysis of IgG antibody responses to Plasmodium falciparum antigens in relation to changing malaria epidemiology in a West African setting
Coordinated scaled-up malaria control interventions have substantially contributed to the dramatic decrease of malaria-related morbidity and mortality in several endemic countries, including Senegal. However, the impacts of a given malaria control intervention on vector and parasite populations, acq...
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Published in: | Malaria journal 2017-07, Vol.16 (1), p.283-283, Article 283 |
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creator | Niang, Makhtar Niass, Oumy Diagne, Nafissatou Sarr, Fatoumata Diene Faye, Michel Matar Diop, Fode Diouf, Babacar Faye, Joseph Badiane, Abdoulaye Perraut, Ronald Sokhna, Cheikh Trape, Jean-François Tall, Adama Toure-Balde, Aissatou |
description | Coordinated scaled-up malaria control interventions have substantially contributed to the dramatic decrease of malaria-related morbidity and mortality in several endemic countries, including Senegal. However, the impacts of a given malaria control intervention on vector and parasite populations, acquired immunity, and disease burden remain very poorly documented largely due to the lack of continuous surveys. This study took advantage of the sera bank established as part of the Dielmo longitudinal project to investigate the dynamics of IgG antibody responses that accompanied the epidemiological changes resulting from malaria control interventions. Schizonts crude extract of a local strain of Plasmodium falciparum (Pfsch07/03) was used in ELISA to measure and compare seroprevalence and magnitude of IgG antibody responses from 2000 to 2012.
The prevalence of Pfsch07/03 IgG antibody responses progressively decreased from 97.25% in 2000 to 57.3% in 2012. The prevalence of Pfsch07/03 antibodies categorized between three different age groups (15 years) revealed increased seroprevalence with age ranging from 47.19 to 62.67 and 89.45%, respectively in (15 years) old age groups. A marked drop in seroprevalence was observed after 2008 and was significant in the younger (15 years (p = 1.00).
The study revealed a substantial contribution of all malaria control interventions to the decrease of IgG antibodies responses to Pfsch07/03 throughout prevention of human-mosquitos contacts, or reduction of parasite biomass. The present study demonstrates the wider potential of sero-epidemiological analysis in monitoring changes in malaria transmission resulting from a given malaria control intervention. |
doi_str_mv | 10.1186/s12936-017-1928-3 |
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The prevalence of Pfsch07/03 IgG antibody responses progressively decreased from 97.25% in 2000 to 57.3% in 2012. The prevalence of Pfsch07/03 antibodies categorized between three different age groups (<7, 7-15, and >15 years) revealed increased seroprevalence with age ranging from 47.19 to 62.67 and 89.45%, respectively in (<7, 7-15, and >15 years) old age groups. A marked drop in seroprevalence was observed after 2008 and was significant in the younger (<7 years) and intermediate (7-15 years) age groups, unlike older individuals aged >15 years (p = 1.00).
The study revealed a substantial contribution of all malaria control interventions to the decrease of IgG antibodies responses to Pfsch07/03 throughout prevention of human-mosquitos contacts, or reduction of parasite biomass. The present study demonstrates the wider potential of sero-epidemiological analysis in monitoring changes in malaria transmission resulting from a given malaria control intervention.</description><identifier>ISSN: 1475-2875</identifier><identifier>EISSN: 1475-2875</identifier><identifier>DOI: 10.1186/s12936-017-1928-3</identifier><identifier>PMID: 28693608</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Adolescent ; Adult ; Age groups ; Aged ; Aged, 80 and over ; Antibodies ; Antibodies, Protozoan - blood ; Antigens ; Antigens, Protozoan - immunology ; Aquatic insects ; Child ; Child, Preschool ; Communicable Disease Control ; Control ; Controls ; Cross-Sectional Studies ; Disease transmission ; ELISA ; Epidemiology ; Erythrocytes ; Female ; Health aspects ; Human diseases ; Humans ; Immunity ; Immunoglobulin G ; Immunoglobulin G - blood ; Immunoglobulins ; Immunology ; Malaria ; Malaria, Falciparum - epidemiology ; Malaria, Falciparum - immunology ; Male ; Middle Aged ; Morbidity ; Mortality ; Parasites ; Plasmodium falciparum ; Plasmodium falciparum - immunology ; Population ; Prevalence ; Schizonts ; Senegal - epidemiology ; Seroepidemiologic Studies ; Serology ; Studies ; Surveys ; Transmission ; Vector-borne diseases ; Young Adult</subject><ispartof>Malaria journal, 2017-07, Vol.16 (1), p.283-283, Article 283</ispartof><rights>COPYRIGHT 2017 BioMed Central Ltd.</rights><rights>2017. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c560t-34ee5503abf17c81569e23666550f2af9e6ecb3e3576bd5b4a35eede7b20611b3</citedby><cites>FETCH-LOGICAL-c560t-34ee5503abf17c81569e23666550f2af9e6ecb3e3576bd5b4a35eede7b20611b3</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/PMC5504683/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2348321594?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28693608$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Niang, Makhtar</creatorcontrib><creatorcontrib>Niass, Oumy</creatorcontrib><creatorcontrib>Diagne, Nafissatou</creatorcontrib><creatorcontrib>Sarr, Fatoumata Diene</creatorcontrib><creatorcontrib>Faye, Michel Matar</creatorcontrib><creatorcontrib>Diop, Fode</creatorcontrib><creatorcontrib>Diouf, Babacar</creatorcontrib><creatorcontrib>Faye, Joseph</creatorcontrib><creatorcontrib>Badiane, Abdoulaye</creatorcontrib><creatorcontrib>Perraut, Ronald</creatorcontrib><creatorcontrib>Sokhna, Cheikh</creatorcontrib><creatorcontrib>Trape, Jean-François</creatorcontrib><creatorcontrib>Tall, Adama</creatorcontrib><creatorcontrib>Toure-Balde, Aissatou</creatorcontrib><title>Temporal analysis of IgG antibody responses to Plasmodium falciparum antigens in relation to changing malaria epidemiology in a West African setting</title><title>Malaria journal</title><addtitle>Malar J</addtitle><description>Coordinated scaled-up malaria control interventions have substantially contributed to the dramatic decrease of malaria-related morbidity and mortality in several endemic countries, including Senegal. However, the impacts of a given malaria control intervention on vector and parasite populations, acquired immunity, and disease burden remain very poorly documented largely due to the lack of continuous surveys. This study took advantage of the sera bank established as part of the Dielmo longitudinal project to investigate the dynamics of IgG antibody responses that accompanied the epidemiological changes resulting from malaria control interventions. Schizonts crude extract of a local strain of Plasmodium falciparum (Pfsch07/03) was used in ELISA to measure and compare seroprevalence and magnitude of IgG antibody responses from 2000 to 2012.
The prevalence of Pfsch07/03 IgG antibody responses progressively decreased from 97.25% in 2000 to 57.3% in 2012. The prevalence of Pfsch07/03 antibodies categorized between three different age groups (<7, 7-15, and >15 years) revealed increased seroprevalence with age ranging from 47.19 to 62.67 and 89.45%, respectively in (<7, 7-15, and >15 years) old age groups. A marked drop in seroprevalence was observed after 2008 and was significant in the younger (<7 years) and intermediate (7-15 years) age groups, unlike older individuals aged >15 years (p = 1.00).
The study revealed a substantial contribution of all malaria control interventions to the decrease of IgG antibodies responses to Pfsch07/03 throughout prevention of human-mosquitos contacts, or reduction of parasite biomass. The present study demonstrates the wider potential of sero-epidemiological analysis in monitoring changes in malaria transmission resulting from a given malaria control intervention.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Age groups</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antibodies</subject><subject>Antibodies, Protozoan - blood</subject><subject>Antigens</subject><subject>Antigens, Protozoan - immunology</subject><subject>Aquatic insects</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Communicable Disease Control</subject><subject>Control</subject><subject>Controls</subject><subject>Cross-Sectional Studies</subject><subject>Disease transmission</subject><subject>ELISA</subject><subject>Epidemiology</subject><subject>Erythrocytes</subject><subject>Female</subject><subject>Health aspects</subject><subject>Human diseases</subject><subject>Humans</subject><subject>Immunity</subject><subject>Immunoglobulin G</subject><subject>Immunoglobulin G - blood</subject><subject>Immunoglobulins</subject><subject>Immunology</subject><subject>Malaria</subject><subject>Malaria, Falciparum - epidemiology</subject><subject>Malaria, Falciparum - immunology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Morbidity</subject><subject>Mortality</subject><subject>Parasites</subject><subject>Plasmodium falciparum</subject><subject>Plasmodium falciparum - immunology</subject><subject>Population</subject><subject>Prevalence</subject><subject>Schizonts</subject><subject>Senegal - epidemiology</subject><subject>Seroepidemiologic Studies</subject><subject>Serology</subject><subject>Studies</subject><subject>Surveys</subject><subject>Transmission</subject><subject>Vector-borne diseases</subject><subject>Young Adult</subject><issn>1475-2875</issn><issn>1475-2875</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkstu1DAUhiMEoqXwAGyQJTZsUnyJL9kgjSooI1WCRRFLy3ZOUo8SO9gZpHkPHhinU0qLkBe2j7_z2-f4r6rXBJ8TosT7TGjLRI2JrElLVc2eVKekkbymSvKnD9Yn1Yucd7iAStLn1QlVoiRidVr9uoZpjsmMyAQzHrLPKPZoO1yW_eJt7A4oQZ5jyJDREtHX0eQpdn4_od6Mzs8mleXKDhAy8qHgo1l8DCvtbkwYfBjQZEaTvEEw-w4mH8c4HFbYoO-QF7Tpk3cmoAzLUvCX1bMinuHV3XxWffv08fric3315XJ7sbmqHRd4qVkDwDlmxvZEOkW4aIEyIUQJ9tT0LQhwlgHjUtiO28YwDtCBtBQLQiw7q7ZH3S6anZ6Tn0w66Gi8vg3ENGiTFu9G0L3DRY9TJ5RtesVtZ6US0DoBxCqFi9aHo9a8txN0DsJSuvpI9PFJ8Dd6iD91eWwjFCsC7-4EUvyxL13Rk88OxtEEiPusSUtkKyQmvKBv_0F3cZ_K_2VNWaMYJbxt_lKDKQX40Mdyr1tF9YYTwiiWt9T5f6gy1n9yMUDvS_xRAjkmuBRzTtDf10iwXm2pj7bUxW16taVea3vzsDn3GX98yH4Dw5ffwA</recordid><startdate>20170711</startdate><enddate>20170711</enddate><creator>Niang, Makhtar</creator><creator>Niass, Oumy</creator><creator>Diagne, Nafissatou</creator><creator>Sarr, Fatoumata Diene</creator><creator>Faye, Michel Matar</creator><creator>Diop, Fode</creator><creator>Diouf, Babacar</creator><creator>Faye, Joseph</creator><creator>Badiane, Abdoulaye</creator><creator>Perraut, Ronald</creator><creator>Sokhna, Cheikh</creator><creator>Trape, Jean-François</creator><creator>Tall, Adama</creator><creator>Toure-Balde, Aissatou</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</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>3V.</scope><scope>7SS</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>F1W</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>H95</scope><scope>H97</scope><scope>K9.</scope><scope>L.G</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20170711</creationdate><title>Temporal analysis of IgG antibody responses to Plasmodium falciparum antigens in relation to changing malaria epidemiology in a West African setting</title><author>Niang, Makhtar ; Niass, Oumy ; Diagne, Nafissatou ; Sarr, Fatoumata Diene ; Faye, Michel Matar ; Diop, Fode ; Diouf, Babacar ; Faye, Joseph ; Badiane, Abdoulaye ; Perraut, Ronald ; Sokhna, Cheikh ; Trape, Jean-François ; Tall, Adama ; Toure-Balde, Aissatou</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c560t-34ee5503abf17c81569e23666550f2af9e6ecb3e3576bd5b4a35eede7b20611b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Age groups</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antibodies</topic><topic>Antibodies, Protozoan - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Malaria journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Niang, Makhtar</au><au>Niass, Oumy</au><au>Diagne, Nafissatou</au><au>Sarr, Fatoumata Diene</au><au>Faye, Michel Matar</au><au>Diop, Fode</au><au>Diouf, Babacar</au><au>Faye, Joseph</au><au>Badiane, Abdoulaye</au><au>Perraut, Ronald</au><au>Sokhna, Cheikh</au><au>Trape, Jean-François</au><au>Tall, Adama</au><au>Toure-Balde, Aissatou</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Temporal analysis of IgG antibody responses to Plasmodium falciparum antigens in relation to changing malaria epidemiology in a West African setting</atitle><jtitle>Malaria journal</jtitle><addtitle>Malar J</addtitle><date>2017-07-11</date><risdate>2017</risdate><volume>16</volume><issue>1</issue><spage>283</spage><epage>283</epage><pages>283-283</pages><artnum>283</artnum><issn>1475-2875</issn><eissn>1475-2875</eissn><abstract>Coordinated scaled-up malaria control interventions have substantially contributed to the dramatic decrease of malaria-related morbidity and mortality in several endemic countries, including Senegal. However, the impacts of a given malaria control intervention on vector and parasite populations, acquired immunity, and disease burden remain very poorly documented largely due to the lack of continuous surveys. This study took advantage of the sera bank established as part of the Dielmo longitudinal project to investigate the dynamics of IgG antibody responses that accompanied the epidemiological changes resulting from malaria control interventions. Schizonts crude extract of a local strain of Plasmodium falciparum (Pfsch07/03) was used in ELISA to measure and compare seroprevalence and magnitude of IgG antibody responses from 2000 to 2012.
The prevalence of Pfsch07/03 IgG antibody responses progressively decreased from 97.25% in 2000 to 57.3% in 2012. The prevalence of Pfsch07/03 antibodies categorized between three different age groups (<7, 7-15, and >15 years) revealed increased seroprevalence with age ranging from 47.19 to 62.67 and 89.45%, respectively in (<7, 7-15, and >15 years) old age groups. A marked drop in seroprevalence was observed after 2008 and was significant in the younger (<7 years) and intermediate (7-15 years) age groups, unlike older individuals aged >15 years (p = 1.00).
The study revealed a substantial contribution of all malaria control interventions to the decrease of IgG antibodies responses to Pfsch07/03 throughout prevention of human-mosquitos contacts, or reduction of parasite biomass. The present study demonstrates the wider potential of sero-epidemiological analysis in monitoring changes in malaria transmission resulting from a given malaria control intervention.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>28693608</pmid><doi>10.1186/s12936-017-1928-3</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Age groups Aged Aged, 80 and over Antibodies Antibodies, Protozoan - blood Antigens Antigens, Protozoan - immunology Aquatic insects Child Child, Preschool Communicable Disease Control Control Controls Cross-Sectional Studies Disease transmission ELISA Epidemiology Erythrocytes Female Health aspects Human diseases Humans Immunity Immunoglobulin G Immunoglobulin G - blood Immunoglobulins Immunology Malaria Malaria, Falciparum - epidemiology Malaria, Falciparum - immunology Male Middle Aged Morbidity Mortality Parasites Plasmodium falciparum Plasmodium falciparum - immunology Population Prevalence Schizonts Senegal - epidemiology Seroepidemiologic Studies Serology Studies Surveys Transmission Vector-borne diseases Young Adult |
title | Temporal analysis of IgG antibody responses to Plasmodium falciparum antigens in relation to changing malaria epidemiology in a West African setting |
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