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Changes in Cytokine, Filarial Antigen, and DNA Levels Associated With Adverse Events Following Treatment of Lymphatic Filariasis

BACKGROUND: Mild to moderate adverse events (AEs) are common after treatment of lymphatic filariasis (LF) and pose a major challenge for the global LF elimination program. We studied changes in cytokine levels and filarial worm components in plasma of subjects with and without AEs following treatmen...

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Autores principales: Andersen, Britt J, Kumar, Jessica, Curtis, Kurt, Sanuku, Nelly, Satofan, Samson, King, Christopher L, Fischer, Peter U, Weil, Gary J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5853815/
https://www.ncbi.nlm.nih.gov/pubmed/29149303
http://dx.doi.org/10.1093/infdis/jix578
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author Andersen, Britt J
Kumar, Jessica
Curtis, Kurt
Sanuku, Nelly
Satofan, Samson
King, Christopher L
Fischer, Peter U
Weil, Gary J
author_facet Andersen, Britt J
Kumar, Jessica
Curtis, Kurt
Sanuku, Nelly
Satofan, Samson
King, Christopher L
Fischer, Peter U
Weil, Gary J
author_sort Andersen, Britt J
collection PubMed
description BACKGROUND: Mild to moderate adverse events (AEs) are common after treatment of lymphatic filariasis (LF) and pose a major challenge for the global LF elimination program. We studied changes in cytokine levels and filarial worm components in plasma of subjects with and without AEs following treatment of LF. METHODS: Participants (n = 24) were hospitalized and monitored for AEs following treatment. Cytokines (27), filarial DNA, circulating filarial antigen (CFA), and immune complexes were measured in plasma samples collected before and after treatment. RESULTS: Levels for 16 cytokines increased after treatment in individuals with moderate AEs compared to individuals with no and/or mild AEs. These included 3 major proinflammatory cytokines (interleukin 6, tumor necrosis factor α, and interleukin 1β). Eotaxin-1 levels were elevated at baseline in individuals who developed moderate AEs after treatment; thus, eotaxin-1 is a potential biomarker for AE risk. CFA and filarial DNA levels increased more in individuals with moderate AEs after treatment than in people with no/mild AEs. CONCLUSIONS: Increases in cytokine, filarial DNA, and CFA levels were associated with development of AEs following treatment of LF. Improved understanding of the pathogenesis of AEs may lead to improved methods for their prevention or management that could increase compliance in elimination programs.
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spelling pubmed-58538152018-03-23 Changes in Cytokine, Filarial Antigen, and DNA Levels Associated With Adverse Events Following Treatment of Lymphatic Filariasis Andersen, Britt J Kumar, Jessica Curtis, Kurt Sanuku, Nelly Satofan, Samson King, Christopher L Fischer, Peter U Weil, Gary J J Infect Dis Major Articles and Brief Reports BACKGROUND: Mild to moderate adverse events (AEs) are common after treatment of lymphatic filariasis (LF) and pose a major challenge for the global LF elimination program. We studied changes in cytokine levels and filarial worm components in plasma of subjects with and without AEs following treatment of LF. METHODS: Participants (n = 24) were hospitalized and monitored for AEs following treatment. Cytokines (27), filarial DNA, circulating filarial antigen (CFA), and immune complexes were measured in plasma samples collected before and after treatment. RESULTS: Levels for 16 cytokines increased after treatment in individuals with moderate AEs compared to individuals with no and/or mild AEs. These included 3 major proinflammatory cytokines (interleukin 6, tumor necrosis factor α, and interleukin 1β). Eotaxin-1 levels were elevated at baseline in individuals who developed moderate AEs after treatment; thus, eotaxin-1 is a potential biomarker for AE risk. CFA and filarial DNA levels increased more in individuals with moderate AEs after treatment than in people with no/mild AEs. CONCLUSIONS: Increases in cytokine, filarial DNA, and CFA levels were associated with development of AEs following treatment of LF. Improved understanding of the pathogenesis of AEs may lead to improved methods for their prevention or management that could increase compliance in elimination programs. Oxford University Press 2018-01-15 2017-11-15 /pmc/articles/PMC5853815/ /pubmed/29149303 http://dx.doi.org/10.1093/infdis/jix578 Text en © The Author(s) 2018. Published by Oxford University Press for the Infectious Diseases Society of America. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Major Articles and Brief Reports
Andersen, Britt J
Kumar, Jessica
Curtis, Kurt
Sanuku, Nelly
Satofan, Samson
King, Christopher L
Fischer, Peter U
Weil, Gary J
Changes in Cytokine, Filarial Antigen, and DNA Levels Associated With Adverse Events Following Treatment of Lymphatic Filariasis
title Changes in Cytokine, Filarial Antigen, and DNA Levels Associated With Adverse Events Following Treatment of Lymphatic Filariasis
title_full Changes in Cytokine, Filarial Antigen, and DNA Levels Associated With Adverse Events Following Treatment of Lymphatic Filariasis
title_fullStr Changes in Cytokine, Filarial Antigen, and DNA Levels Associated With Adverse Events Following Treatment of Lymphatic Filariasis
title_full_unstemmed Changes in Cytokine, Filarial Antigen, and DNA Levels Associated With Adverse Events Following Treatment of Lymphatic Filariasis
title_short Changes in Cytokine, Filarial Antigen, and DNA Levels Associated With Adverse Events Following Treatment of Lymphatic Filariasis
title_sort changes in cytokine, filarial antigen, and dna levels associated with adverse events following treatment of lymphatic filariasis
topic Major Articles and Brief Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5853815/
https://www.ncbi.nlm.nih.gov/pubmed/29149303
http://dx.doi.org/10.1093/infdis/jix578
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