Changes in Antibody Levels during and following an Episode of Acute Adenolymphangitis (ADL) among Lymphedema Patients in Léogâne, Haiti.
Identifieur interne : 000B69 ( PubMed/Curation ); précédent : 000B68; suivant : 000B70Changes in Antibody Levels during and following an Episode of Acute Adenolymphangitis (ADL) among Lymphedema Patients in Léogâne, Haiti.
Auteurs : Katherine E. Mues [États-Unis] ; Patrick J. Lammie [États-Unis] ; Mitchel Klein [États-Unis] ; David G. Kleinbaum [États-Unis] ; David Addiss [États-Unis] ; Leanne M. Fox [États-Unis]Source :
- PloS one [ 1932-6203 ] ; 2015.
Descripteurs français
- KwdFr :
- Adulte, Animaux, Anticorps antibactériens (immunologie), Anticorps antibactériens (sang), Anticorps antifongiques (immunologie), Anticorps antifongiques (sang), Anticorps antiprotozoaires (immunologie), Anticorps antiprotozoaires (sang), Femelle, Filariose lymphatique (étiologie), Haïti, Humains, Lymphangite (immunologie), Lymphangite (sang), Lymphangite (étiologie), Lymphoedème (immunologie), Lymphoedème (sang), Mâle, Streptococcus pyogenes (immunologie), Wuchereria bancrofti (immunologie), Études de cohortes.
- MESH :
- immunologie : Anticorps antibactériens, Anticorps antifongiques, Anticorps antiprotozoaires, Lymphangite, Lymphoedème, Streptococcus pyogenes, Wuchereria bancrofti.
- sang : Anticorps antibactériens, Anticorps antifongiques, Anticorps antiprotozoaires, Lymphangite, Lymphoedème.
- étiologie : Filariose lymphatique, Lymphangite.
- Adulte, Animaux, Femelle, Haïti, Humains, Mâle, Études de cohortes.
- Wicri :
- geographic : Haïti.
English descriptors
- KwdEn :
- Adult, Animals, Antibodies, Bacterial (blood), Antibodies, Bacterial (immunology), Antibodies, Fungal (blood), Antibodies, Fungal (immunology), Antibodies, Protozoan (blood), Antibodies, Protozoan (immunology), Cohort Studies, Elephantiasis, Filarial (etiology), Female, Haiti, Humans, Lymphangitis (blood), Lymphangitis (etiology), Lymphangitis (immunology), Lymphedema (blood), Lymphedema (immunology), Male, Streptococcus pyogenes (immunology), Wuchereria bancrofti (immunology).
- MESH :
- chemical , blood : Antibodies, Bacterial, Antibodies, Fungal, Antibodies, Protozoan.
- chemical , immunology : Antibodies, Bacterial, Antibodies, Fungal, Antibodies, Protozoan.
- geographic : Haiti.
- blood : Lymphangitis, Lymphedema.
- etiology : Elephantiasis, Filarial, Lymphangitis.
- immunology : Lymphangitis, Lymphedema, Streptococcus pyogenes, Wuchereria bancrofti.
- Adult, Animals, Cohort Studies, Female, Humans, Male.
Abstract
Episodes of acute adenolymphangitis (ADL) are often the first clinical sign of lymphatic filariasis (LF). They are often accompanied by swelling of the affected limb, inflammation, fever, and general malaise and lead to the progression of lymphedema. Although ADL episodes have been studied for a century or more, questions still remain as to their etiology. We quantified antibody levels to pathogens that potentially contribute to ADL episodes during and after an episode among lymphedema patients in Léogâne, Haiti. We estimated the proportion of ADL episodes hypothesized to be attributed to specific pathogens.
DOI: 10.1371/journal.pone.0141047
PubMed: 26492462
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pubmed:26492462Le document en format XML
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They are often accompanied by swelling of the affected limb, inflammation, fever, and general malaise and lead to the progression of lymphedema. Although ADL episodes have been studied for a century or more, questions still remain as to their etiology. We quantified antibody levels to pathogens that potentially contribute to ADL episodes during and after an episode among lymphedema patients in Léogâne, Haiti. We estimated the proportion of ADL episodes hypothesized to be attributed to specific pathogens.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">26492462</PMID><DateCreated><Year>2015</Year><Month>10</Month><Day>23</Day></DateCreated><DateCompleted><Year>2016</Year><Month>06</Month><Day>30</Day></DateCompleted><DateRevised><Year>2015</Year><Month>10</Month><Day>30</Day></DateRevised><Article PubModel="Electronic-eCollection"><Journal><ISSN IssnType="Electronic">1932-6203</ISSN><JournalIssue CitedMedium="Internet"><Volume>10</Volume><Issue>10</Issue><PubDate><Year>2015</Year></PubDate></JournalIssue><Title>PloS one</Title><ISOAbbreviation>PLoS ONE</ISOAbbreviation></Journal><ArticleTitle>Changes in Antibody Levels during and following an Episode of Acute Adenolymphangitis (ADL) among Lymphedema Patients in Léogâne, Haiti.</ArticleTitle><Pagination><MedlinePgn>e0141047</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1371/journal.pone.0141047</ELocationID><Abstract><AbstractText Label="INTRODUCTION" NlmCategory="BACKGROUND">Episodes of acute adenolymphangitis (ADL) are often the first clinical sign of lymphatic filariasis (LF). They are often accompanied by swelling of the affected limb, inflammation, fever, and general malaise and lead to the progression of lymphedema. Although ADL episodes have been studied for a century or more, questions still remain as to their etiology. We quantified antibody levels to pathogens that potentially contribute to ADL episodes during and after an episode among lymphedema patients in Léogâne, Haiti. We estimated the proportion of ADL episodes hypothesized to be attributed to specific pathogens.</AbstractText><AbstractText Label="METHODS" NlmCategory="METHODS">We measured antibody levels to specific pathogens during and following an ADL episode among 41 lymphedema patients enrolled in a cohort study in Léogâne, Haiti. We calculated the absolute and relative changes in antibody levels between the ADL and convalescent time points. We calculated the proportion of episodes that demonstrated a two-fold increase in antibody level for several bacterial, fungal, and filarial pathogens.</AbstractText><AbstractText Label="RESULTS" NlmCategory="RESULTS">Our results showed the greatest proportion of two-fold changes in antibody levels for the carbohydrate antigen Streptococcus group A, followed by IgG2 responses to a soluble filarial antigen (BpG2), Streptococcal Pyrogenic Exotoxin B, and an antigen for the fungal pathogen Candida. When comparing the median antibody level during the ADL episode to the median antibody level at the convalescent time point, only the antigens for Pseudomonas species (P-value = 0.0351) and Streptolysin O (P-value = 0.0074) showed a significant result.</AbstractText><AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Although our results are limited by the lack of a control group and few antibody responses, they provide some evidence for infection with Streptococcus A as a potential contributing factor to ADL episodes. Our results add to the current evidence and illustrate the importance of determining the causal role of bacterial and fungal pathogens and immunological antifilarial response in ADL episodes.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Mues</LastName><ForeName>Katherine E</ForeName><Initials>KE</Initials><AffiliationInfo><Affiliation>Department of Epidemiology, Rollins School of Public Health and Laney Graduate School, Emory University, Atlanta, Georgia, United States of America.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Lammie</LastName><ForeName>Patrick J</ForeName><Initials>PJ</Initials><AffiliationInfo><Affiliation>Parasitic Diseases Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Klein</LastName><ForeName>Mitchel</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Department of Epidemiology, Rollins School of Public Health and Laney Graduate School, Emory University, Atlanta, Georgia, United States of America.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Kleinbaum</LastName><ForeName>David G</ForeName><Initials>DG</Initials><AffiliationInfo><Affiliation>Department of Epidemiology, Rollins School of Public Health and Laney Graduate School, Emory University, Atlanta, Georgia, United States of America.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Addiss</LastName><ForeName>David</ForeName><Initials>D</Initials><AffiliationInfo><Affiliation>Task Force for Global Health, Decatur, Georgia, United States of America.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Fox</LastName><ForeName>LeAnne M</ForeName><Initials>LM</Initials><AffiliationInfo><Affiliation>Parasitic Diseases Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2015</Year><Month>10</Month><Day>22</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>PLoS One</MedlineTA><NlmUniqueID>101285081</NlmUniqueID><ISSNLinking>1932-6203</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000907">Antibodies, Bacterial</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000908">Antibodies, Fungal</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000913">Antibodies, Protozoan</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Am J Epidemiol. 1978 Dec;108(6):447-53</RefSource><PMID Version="1">736024</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Infect Immun. 1996 Sep;64(9):3461-6</RefSource><PMID Version="1">8751885</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Trop Med Int Health. 2003 Dec;8(12):1102-9</RefSource><PMID Version="1">14641845</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Trop Med Int Health. 2003 Jan;8(1):56-9</RefSource><PMID Version="1">12535251</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>N Engl J Med. 2002 Dec 5;347(23):1841-8</RefSource><PMID 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Source="NLM">PMC4619626</OtherID></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2015</Year><Month>07</Month><Day>27</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2015</Year><Month>10</Month><Day>02</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2015</Year><Month>10</Month><Day>23</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2015</Year><Month>10</Month><Day>23</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2016</Year><Month>7</Month><Day>1</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>epublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">26492462</ArticleId><ArticleId IdType="doi">10.1371/journal.pone.0141047</ArticleId><ArticleId IdType="pii">PONE-D-15-32812</ArticleId><ArticleId IdType="pmc">PMC4619626</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce 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