Serveur d'exploration sur le lymphœdème

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Detection of Serum IgG Antibodies Specific for Wolbachia Surface Protein in Rhesus Monkeys Infected with Brugia malayi

Identifieur interne : 009B84 ( Main/Exploration ); précédent : 009B83; suivant : 009B85

Detection of Serum IgG Antibodies Specific for Wolbachia Surface Protein in Rhesus Monkeys Infected with Brugia malayi

Auteurs : George A. Punkosdy [Géorgie (pays)] ; Vida A. Dennis [États-Unis] ; Barbara L. Lasater [États-Unis] ; George Tzertzinis [États-Unis] ; Jeremy M. Foster [États-Unis] ; Patrick J. Lammie [Géorgie (pays)]

Source :

RBID : ISTEX:6C00FDF13A2963AABFD4B1931452EDEB724EF92B

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English descriptors

Abstract

The mechanism of lymphedema development in individuals with lymphatic filariasis is presently poorly understood. To investigate whether Wolbachia, symbiotic bacteria living within filarial nematodes, may be involved in disease progression, Wolbachia‐specific immune responses were assayed in a group of Brugia malayi–infected rhesus monkeys. Serum IgG antibodies specific for a major Wolbachia surface protein (WSP) were detected in 2 of 12 infected monkeys. It is interesting that both of these monkeys developed lymphedema after becoming amicrofilaremic. WSP‐specific antibody responses were temporally associated with increases in antifilarial IgG1 antibodies as well as lymphedema development. These findings suggest that Wolbachia may be important in understanding disease caused by filarial worms.

Url:
DOI: 10.1086/322023


Affiliations:


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Le document en format XML

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<term>Animals</term>
<term>Antibodies, Bacterial (blood)</term>
<term>Antibody</term>
<term>Antibody Specificity</term>
<term>Bacterial Proteins (genetics)</term>
<term>Bacterial Proteins (immunology)</term>
<term>Base Sequence</term>
<term>Brugia malayi</term>
<term>Cloning, Molecular</term>
<term>Detection</term>
<term>Development</term>
<term>Disease Models, Animal</term>
<term>Disease Progression</term>
<term>Filariosis</term>
<term>Humans</term>
<term>IgG</term>
<term>Immune response</term>
<term>Immunoglobulin G (blood)</term>
<term>Lymphedema</term>
<term>Lymphedema (etiology)</term>
<term>Lymphedema (immunology)</term>
<term>Macaca mulatta</term>
<term>Male</term>
<term>Membrane Proteins (genetics)</term>
<term>Membrane Proteins (immunology)</term>
<term>Molecular Sequence Data</term>
<term>Monkey</term>
<term>Nematode disease</term>
<term>Protein</term>
<term>Recombinant Fusion Proteins (immunology)</term>
<term>Rickettsia Infections (blood)</term>
<term>Rickettsia Infections (complications)</term>
<term>Rickettsia Infections (immunology)</term>
<term>Serum</term>
<term>Specificity</term>
<term>Time Factors</term>
<term>Wolbachia</term>
<term>Wolbachia (immunology)</term>
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<term>Animaux</term>
<term>Anticorps antibactériens (sang)</term>
<term>Clonage moléculaire</term>
<term>Données de séquences moléculaires</term>
<term>Facteurs temps</term>
<term>Humains</term>
<term>Immunoglobuline G (sang)</term>
<term>Lymphoedème (immunologie)</term>
<term>Lymphoedème (étiologie)</term>
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<term>Modèles animaux de maladie humaine</term>
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<term>Protéines bactériennes (génétique)</term>
<term>Protéines bactériennes (immunologie)</term>
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<term>Protéines membranaires (génétique)</term>
<term>Protéines membranaires (immunologie)</term>
<term>Rickettsioses ()</term>
<term>Rickettsioses (immunologie)</term>
<term>Rickettsioses (sang)</term>
<term>Spécificité des anticorps</term>
<term>Séquence nucléotidique</term>
<term>Wolbachia (immunologie)</term>
<term>Évolution de la maladie</term>
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<term>Antibodies, Bacterial</term>
<term>Immunoglobulin G</term>
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<term>Membrane Proteins</term>
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<term>Bacterial Proteins</term>
<term>Membrane Proteins</term>
<term>Recombinant Fusion Proteins</term>
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<term>Rickettsia Infections</term>
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<keywords scheme="MESH" qualifier="complications" xml:lang="en">
<term>Rickettsia Infections</term>
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<term>Lymphedema</term>
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<term>Protéines bactériennes</term>
<term>Protéines membranaires</term>
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<term>Lymphoedème</term>
<term>Protéines bactériennes</term>
<term>Protéines de fusion recombinantes</term>
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<term>Wolbachia</term>
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<term>Anticorps antibactériens</term>
<term>Immunoglobuline G</term>
<term>Rickettsioses</term>
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<keywords scheme="MESH" qualifier="étiologie" xml:lang="fr">
<term>Lymphoedème</term>
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<term>Animals</term>
<term>Antibody Specificity</term>
<term>Base Sequence</term>
<term>Cloning, Molecular</term>
<term>Disease Models, Animal</term>
<term>Disease Progression</term>
<term>Humans</term>
<term>Macaca mulatta</term>
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<term>Time Factors</term>
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<term>Données de séquences moléculaires</term>
<term>Facteurs temps</term>
<term>Humains</term>
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<term>Modèles animaux de maladie humaine</term>
<term>Mâle</term>
<term>Rickettsioses</term>
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<term>Anticorps</term>
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<front>
<div type="abstract">The mechanism of lymphedema development in individuals with lymphatic filariasis is presently poorly understood. To investigate whether Wolbachia, symbiotic bacteria living within filarial nematodes, may be involved in disease progression, Wolbachia‐specific immune responses were assayed in a group of Brugia malayi–infected rhesus monkeys. Serum IgG antibodies specific for a major Wolbachia surface protein (WSP) were detected in 2 of 12 infected monkeys. It is interesting that both of these monkeys developed lymphedema after becoming amicrofilaremic. WSP‐specific antibody responses were temporally associated with increases in antifilarial IgG1 antibodies as well as lymphedema development. These findings suggest that Wolbachia may be important in understanding disease caused by filarial worms.</div>
</front>
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