LymphedemaV1, Ncbi, Merge, bibRecord, 008894

Positivity of Antigen Tests Used for Diagnosis of Lymphatic Filariasis in Individuals Without Wuchereria bancrofti Infection But with High Loa loa Microfilaremia.

Identifieur interne : 008894 ( Ncbi/Merge ); précédent : 008893; suivant : 008895

Positivity of Antigen Tests Used for Diagnosis of Lymphatic Filariasis in Individuals Without Wuchereria bancrofti Infection But with High Loa loa Microfilaremia.

Auteurs : Sébastien D. Pion [France] ; Céline Montavon [France] ; Cédric B. Chesnais [France] ; Joseph Kamgno [Cameroun] ; Samuel Wanji [Cameroun] ; Amy D. Klion [États-Unis] ; Thomas B. Nutman [États-Unis] ; Michel Boussinesq [France]

Source :

The American journal of tropical medicine and hygiene [ 1476-1645 ] ; 2016.

RBID : pubmed:27729568

Descripteurs français

KwdFr :
- Adolescent, Adulte, Adulte d'âge moyen, Animaux, Antigènes d'helminthe (sang), Enfant, Enfant d'âge préscolaire, Femelle, Filariose lymphatique (diagnostic), Filariose lymphatique (parasitologie), Humains, Jeune adulte, Loa (isolement et purification), Mâle, Wuchereria bancrofti (isolement et purification).
MESH :
- diagnostic : Filariose lymphatique.
- isolement et purification : Loa, Wuchereria bancrofti.
- parasitologie : Filariose lymphatique.
- sang : Antigènes d'helminthe.
- Adolescent, Adulte, Adulte d'âge moyen, Animaux, Enfant, Enfant d'âge préscolaire, Femelle, Humains, Jeune adulte, Mâle.

English descriptors

KwdEn :
- Adolescent, Adult, Animals, Antigens, Helminth (blood), Child, Child, Preschool, Elephantiasis, Filarial (diagnosis), Elephantiasis, Filarial (parasitology), Female, Humans, Loa (isolation & purification), Male, Middle Aged, Wuchereria bancrofti (isolation & purification), Young Adult.
MESH :
- chemical , blood : Antigens, Helminth.
- diagnosis : Elephantiasis, Filarial.
- isolation & purification : Loa, Wuchereria bancrofti.
- parasitology : Elephantiasis, Filarial.
- Adolescent, Adult, Animals, Child, Child, Preschool, Female, Humans, Male, Middle Aged, Young Adult.

Abstract

Since the mid-2000s, the immunochromatographic card test (ICT), a point-of-care test for detecting Wuchereria bancrofti circulating filarial antigens (CFAs), has been the backbone for mapping and monitoring lymphatic filariasis (LF) worldwide. Recently, there have been instances in which CFA positivity has been associated with Loa loa microfilaremia. Here, we examined the association, at both the community and individual levels, between L. loa and CFA using additional diagnostic tools (quantitative polymerase chain reaction [qPCR], Og4C3 enzyme-linked immunosorbent assay, and IgG4 antibodies to Wb123 assays) to demonstrate the relationship between L. loa microfilaremia and ICT positivity. In May 2013, peripheral blood was collected during the day from 1,812 individuals living in southern Cameroon. ICT tests were done on the spot, and positive individuals were resampled at night. Results of qPCR and Wb123 assays concurred proving the absence of W. bancrofti infection. Og4C3 assays indicate a quantitative relationship between the level of L. loa microfilaremia and that of CFA. This was confirmed by epidemiological analyses, which reveal a strong association between L. loa microfilaremia and ICT positivity, with 50% of ICT reacting to L. loa when its microfilarial density exceeds 30,000 microfilariae/mL. At the community level, the proportion of positive ICT would exceed 2% when the prevalence of L. loa microfilaremia in the total population is above 20%. This has significant implications in terms of mapping and control of LF caused by W. bancrofti in Loa-endemic areas. Cross-reactivity of ICT with L. loa has to be considered in the context of both individual and community diagnostics.

DOI: 10.4269/ajtmh.16-0547
PubMed: 27729568

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<term>Adult</term>
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<term>Child</term>
<term>Child, Preschool</term>
<term>Elephantiasis, Filarial (diagnosis)</term>
<term>Elephantiasis, Filarial (parasitology)</term>
<term>Female</term>
<term>Humans</term>
<term>Loa (isolation & purification)</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Wuchereria bancrofti (isolation & purification)</term>
<term>Young Adult</term>
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<term>Antigènes d'helminthe (sang)</term>
<term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
<term>Filariose lymphatique (diagnostic)</term>
<term>Filariose lymphatique (parasitologie)</term>
<term>Humains</term>
<term>Jeune adulte</term>
<term>Loa (isolement et purification)</term>
<term>Mâle</term>
<term>Wuchereria bancrofti (isolement et purification)</term>
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<keywords scheme="MESH" qualifier="isolation & purification" xml:lang="en"><term>Loa</term>
<term>Wuchereria bancrofti</term>
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<front><div type="abstract" xml:lang="en">Since the mid-2000s, the immunochromatographic card test (ICT), a point-of-care test for detecting Wuchereria bancrofti circulating filarial antigens (CFAs), has been the backbone for mapping and monitoring lymphatic filariasis (LF) worldwide. Recently, there have been instances in which CFA positivity has been associated with Loa loa microfilaremia. Here, we examined the association, at both the community and individual levels, between L. loa and CFA using additional diagnostic tools (quantitative polymerase chain reaction [qPCR], Og4C3 enzyme-linked immunosorbent assay, and IgG4 antibodies to Wb123 assays) to demonstrate the relationship between L. loa microfilaremia and ICT positivity. In May 2013, peripheral blood was collected during the day from 1,812 individuals living in southern Cameroon. ICT tests were done on the spot, and positive individuals were resampled at night. Results of qPCR and Wb123 assays concurred proving the absence of W. bancrofti infection. Og4C3 assays indicate a quantitative relationship between the level of L. loa microfilaremia and that of CFA. This was confirmed by epidemiological analyses, which reveal a strong association between L. loa microfilaremia and ICT positivity, with 50% of ICT reacting to L. loa when its microfilarial density exceeds 30,000 microfilariae/mL. At the community level, the proportion of positive ICT would exceed 2% when the prevalence of L. loa microfilaremia in the total population is above 20%. This has significant implications in terms of mapping and control of LF caused by W. bancrofti in Loa-endemic areas. Cross-reactivity of ICT with L. loa has to be considered in the context of both individual and community diagnostics.</div>
</front>
</TEI>
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<DateCreated><Year>2016</Year>
<Month>10</Month>
<Day>12</Day>
</DateCreated>
<DateCompleted><Year>2017</Year>
<Month>05</Month>
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<JournalIssue CitedMedium="Internet"><Volume>95</Volume>
<Issue>6</Issue>
<PubDate><Year>2016</Year>
<Month>Dec</Month>
<Day>07</Day>
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<Title>The American journal of tropical medicine and hygiene</Title>
<ISOAbbreviation>Am. J. Trop. Med. Hyg.</ISOAbbreviation>
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<ArticleTitle>Positivity of Antigen Tests Used for Diagnosis of Lymphatic Filariasis in Individuals Without Wuchereria bancrofti Infection But with High Loa loa Microfilaremia.</ArticleTitle>
<Pagination><MedlinePgn>1417-1423</MedlinePgn>
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<Abstract><AbstractText>Since the mid-2000s, the immunochromatographic card test (ICT), a point-of-care test for detecting Wuchereria bancrofti circulating filarial antigens (CFAs), has been the backbone for mapping and monitoring lymphatic filariasis (LF) worldwide. Recently, there have been instances in which CFA positivity has been associated with Loa loa microfilaremia. Here, we examined the association, at both the community and individual levels, between L. loa and CFA using additional diagnostic tools (quantitative polymerase chain reaction [qPCR], Og4C3 enzyme-linked immunosorbent assay, and IgG4 antibodies to Wb123 assays) to demonstrate the relationship between L. loa microfilaremia and ICT positivity. In May 2013, peripheral blood was collected during the day from 1,812 individuals living in southern Cameroon. ICT tests were done on the spot, and positive individuals were resampled at night. Results of qPCR and Wb123 assays concurred proving the absence of W. bancrofti infection. Og4C3 assays indicate a quantitative relationship between the level of L. loa microfilaremia and that of CFA. This was confirmed by epidemiological analyses, which reveal a strong association between L. loa microfilaremia and ICT positivity, with 50% of ICT reacting to L. loa when its microfilarial density exceeds 30,000 microfilariae/mL. At the community level, the proportion of positive ICT would exceed 2% when the prevalence of L. loa microfilaremia in the total population is above 20%. This has significant implications in terms of mapping and control of LF caused by W. bancrofti in Loa-endemic areas. Cross-reactivity of ICT with L. loa has to be considered in the context of both individual and community diagnostics.</AbstractText>
<CopyrightInformation>© The American Society of Tropical Medicine and Hygiene.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Pion</LastName>
<ForeName>Sébastien D</ForeName>
<Initials>SD</Initials>
<AffiliationInfo><Affiliation>Unité Mixte Internationale 233, Institut de Recherche pour le Développement, Université de Montpellier, Institut National de la Santé et de la Recherche Médicale, Montpellier, France. sebastien.pion@ird.fr.</Affiliation>
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<AffiliationInfo><Affiliation>Centre de Recherche sur les Filarioses et autres Maladies Tropicales, Yaoundé, Cameroon.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Montavon</LastName>
<ForeName>Céline</ForeName>
<Initials>C</Initials>
<AffiliationInfo><Affiliation>Unité Mixte Internationale 233, Institut de Recherche pour le Développement, Université de Montpellier, Institut National de la Santé et de la Recherche Médicale, Montpellier, France.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Chesnais</LastName>
<ForeName>Cédric B</ForeName>
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<AffiliationInfo><Affiliation>Unité Mixte Internationale 233, Institut de Recherche pour le Développement, Université de Montpellier, Institut National de la Santé et de la Recherche Médicale, Montpellier, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Kamgno</LastName>
<ForeName>Joseph</ForeName>
<Initials>J</Initials>
<AffiliationInfo><Affiliation>Centre de Recherche sur les Filarioses et autres Maladies Tropicales, Yaoundé, Cameroon.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Faculty of Medicine and Biomedical Sciences, University of Yaoundé 1, Yaoundé, Cameroon.</Affiliation>
</AffiliationInfo>
</Author>
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<ForeName>Samuel</ForeName>
<Initials>S</Initials>
<AffiliationInfo><Affiliation>Research Foundation for Tropical Diseases and Environment, Buea, Cameroon.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Department of Microbiology and Parasitology, University of Buea, Buea, Cameroon.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Klion</LastName>
<ForeName>Amy D</ForeName>
<Initials>AD</Initials>
<AffiliationInfo><Affiliation>National Institutes of Health, Bethesda, Maryland.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Nutman</LastName>
<ForeName>Thomas B</ForeName>
<Initials>TB</Initials>
<AffiliationInfo><Affiliation>National Institutes of Health, Bethesda, Maryland.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Boussinesq</LastName>
<ForeName>Michel</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Unité Mixte Internationale 233, Institut de Recherche pour le Développement, Université de Montpellier, Institut National de la Santé et de la Recherche Médicale, Montpellier, France.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
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</PublicationTypeList>
<ArticleDate DateType="Electronic"><Year>2016</Year>
<Month>10</Month>
<Day>10</Day>
</ArticleDate>
</Article>
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<MedlineTA>Am J Trop Med Hyg</MedlineTA>
<NlmUniqueID>0370507</NlmUniqueID>
<ISSNLinking>0002-9637</ISSNLinking>
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<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
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</Chemical>
</ChemicalList>
<CitationSubset>AIM</CitationSubset>
<CitationSubset>IM</CitationSubset>
<CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Am J Trop Med Hyg. 2013 Jul;89(1):11-5</RefSource>
<PMID Version="1">23690552</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>J Infect Dis. 1987 Aug;156(2):350-5</RefSource>
<PMID Version="1">3298458</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Trop Med Int Health. 1999 Aug;4(8):565-74</RefSource>
<PMID Version="1">10499080</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Lancet Glob Health. 2016 Mar;4(3):e154-5</RefSource>
<PMID Version="1">26874545</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Am J Trop Med Hyg. 2013 Nov;89(5):916-8</RefSource>
<PMID Version="1">24019435</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>PLoS Negl Trop Dis. 2012;6(12):e1930</RefSource>
<PMID Version="1">23236529</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Clin Vaccine Immunol. 2015 Aug;22(8):896-901</RefSource>
<PMID Version="1">26018537</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Am J Trop Med Hyg. 2016 Jun 1;94(6):1301-8</RefSource>
<PMID Version="1">27044568</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>PLoS Negl Trop Dis. 2015 Nov 06;9(11):e0004184</RefSource>
<PMID Version="1">26544042</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>PLoS Negl Trop Dis. 2015 Sep 09;9(9):e0004001</RefSource>
<PMID Version="1">26353087</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>J Immunol. 1987 May 1;138(9):3035-41</RefSource>
<PMID Version="1">3553330</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Am J Trop Med Hyg. 2014 Dec;91(6):1142-8</RefSource>
<PMID Version="1">25223938</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>PLoS Negl Trop Dis. 2012;6(12):e1940</RefSource>
<PMID Version="1">23236533</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>PLoS Negl Trop Dis. 2011 Aug;5(8):e1299</RefSource>
<PMID Version="1">21912716</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>PLoS Negl Trop Dis. 2015 Nov 05;9(11):e0004172</RefSource>
<PMID Version="1">26539700</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Clin Vaccine Immunol. 2013 Aug;20(8):1155-61</RefSource>
<PMID Version="1">23740923</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Trop Med Parasitol. 1990 Dec;41(4):403-6</RefSource>
<PMID Version="1">2075384</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Parasit Vectors. 2016 May 05;9:267</RefSource>
<PMID Version="1">27151313</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Am J Trop Med Hyg. 2006 May;74(5):826-32</RefSource>
<PMID Version="1">16687688</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Trans R Soc Trop Med Hyg. 1998 Sep-Oct;92(5):518-21</RefSource>
<PMID Version="1">9861367</PMID>
</CommentsCorrections>
</CommentsCorrectionsList>
<MeshHeadingList><MeshHeading><DescriptorName UI="D000293" MajorTopicYN="N">Adolescent</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D000947" MajorTopicYN="N">Antigens, Helminth</DescriptorName>
<QualifierName UI="Q000097" MajorTopicYN="Y">blood</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002648" MajorTopicYN="N">Child</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002675" MajorTopicYN="N">Child, Preschool</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D004605" MajorTopicYN="N">Elephantiasis, Filarial</DescriptorName>
<QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName>
<QualifierName UI="Q000469" MajorTopicYN="Y">parasitology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008117" MajorTopicYN="N">Loa</DescriptorName>
<QualifierName UI="Q000302" MajorTopicYN="Y">isolation & purification</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D014958" MajorTopicYN="N">Wuchereria bancrofti</DescriptorName>
<QualifierName UI="Q000302" MajorTopicYN="Y">isolation & purification</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D055815" MajorTopicYN="N">Young Adult</DescriptorName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="received"><Year>2016</Year>
<Month>07</Month>
<Day>03</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted"><Year>2016</Year>
<Month>08</Month>
<Day>25</Day>
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<Month>10</Month>
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<Month>5</Month>
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<ArticleIdList><ArticleId IdType="pubmed">27729568</ArticleId>
<ArticleId IdType="pii">ajtmh.16-0547</ArticleId>
<ArticleId IdType="doi">10.4269/ajtmh.16-0547</ArticleId>
<ArticleId IdType="pmc">PMC5154460</ArticleId>
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</pubmed>
<affiliations><list><country><li>Cameroun</li>
<li>France</li>
<li>États-Unis</li>
</country>
<region><li>Languedoc-Roussillon</li>
<li>Maryland</li>
<li>Occitanie (région administrative)</li>
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<settlement><li>Montpellier</li>
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</list>
<tree><country name="France"><region name="Occitanie (région administrative)"><name sortKey="Pion, Sebastien D" sort="Pion, Sebastien D" uniqKey="Pion S" first="Sébastien D" last="Pion">Sébastien D. Pion</name>
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<name sortKey="Wanji, Samuel" sort="Wanji, Samuel" uniqKey="Wanji S" first="Samuel" last="Wanji">Samuel Wanji</name>
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<country name="États-Unis"><region name="Maryland"><name sortKey="Klion, Amy D" sort="Klion, Amy D" uniqKey="Klion A" first="Amy D" last="Klion">Amy D. Klion</name>
</region>
<name sortKey="Nutman, Thomas B" sort="Nutman, Thomas B" uniqKey="Nutman T" first="Thomas B" last="Nutman">Thomas B. Nutman</name>
</country>
</tree>
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</record>

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Positivity of Antigen Tests Used for Diagnosis of Lymphatic Filariasis in Individuals Without Wuchereria bancrofti Infection But with High Loa loa Microfilaremia.

Positivity of Antigen Tests Used for Diagnosis of Lymphatic Filariasis in Individuals Without Wuchereria bancrofti Infection But with High Loa loa Microfilaremia.

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