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Eosinophil Granule Proteins ECP and EPX as Markers for a Potential Early-Stage Inflammatory Lesion in Female Genital Schistosomiasis (FGS)

BACKGROUND: Genital granulomas induced by Schistosoma haematobium eggs can manifest as different lesion types visible by colposcopy; rubbery papules (RP), homogenous sandy patches (HSP) and grainy sandy patches (GSP). Pronounced tissue eosinophilia is a candidate marker for active S. haematobium pat...

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Autores principales: Ramarokoto, Charles Emile, Kildemoes, Anna Overgaard, Randrianasolo, Bodo Sahondra, Ravoniarimbinina, Pascaline, Ravaoalimalala, Vololomboahangy Elisabeth, Leutscher, Peter, Kjetland, Eyrun Floerecke, Vennervald, Birgitte Jyding
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4102437/
https://www.ncbi.nlm.nih.gov/pubmed/25033206
http://dx.doi.org/10.1371/journal.pntd.0002974
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author Ramarokoto, Charles Emile
Kildemoes, Anna Overgaard
Randrianasolo, Bodo Sahondra
Ravoniarimbinina, Pascaline
Ravaoalimalala, Vololomboahangy Elisabeth
Leutscher, Peter
Kjetland, Eyrun Floerecke
Vennervald, Birgitte Jyding
author_facet Ramarokoto, Charles Emile
Kildemoes, Anna Overgaard
Randrianasolo, Bodo Sahondra
Ravoniarimbinina, Pascaline
Ravaoalimalala, Vololomboahangy Elisabeth
Leutscher, Peter
Kjetland, Eyrun Floerecke
Vennervald, Birgitte Jyding
author_sort Ramarokoto, Charles Emile
collection PubMed
description BACKGROUND: Genital granulomas induced by Schistosoma haematobium eggs can manifest as different lesion types visible by colposcopy; rubbery papules (RP), homogenous sandy patches (HSP) and grainy sandy patches (GSP). Pronounced tissue eosinophilia is a candidate marker for active S. haematobium pathology, as viable schistosome egg granulomas often are eosinophil rich. Here it was investigated whether eosinophil granule proteins ECP (eosinophil cationic protein) and EPX (eosinophil protein-X) in urine and genital lavage can be used as markers for active FGS lesions. METHODS: Uro-genital samples from 118 Malagasy women were analysed for ECP and EPX by standard sandwich avidin/biotin amplified ELISA. PRINCIPAL FINDINGS: The women with RP lesions had significantly higher levels of ECP and EPX in both lavage and urine. Furthermore, women with RP lesions were significantly younger than those with GSP. This could indicate that RP lesions might be more recently established and thus represent an earlier inflammatory lesion stage. CONCLUSION: ECP in genital lavage might be a future tool aiding the identification of FGS pathology at a stage where reversibility remains a possibility following praziquantel treatment.
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spelling pubmed-41024372014-07-21 Eosinophil Granule Proteins ECP and EPX as Markers for a Potential Early-Stage Inflammatory Lesion in Female Genital Schistosomiasis (FGS) Ramarokoto, Charles Emile Kildemoes, Anna Overgaard Randrianasolo, Bodo Sahondra Ravoniarimbinina, Pascaline Ravaoalimalala, Vololomboahangy Elisabeth Leutscher, Peter Kjetland, Eyrun Floerecke Vennervald, Birgitte Jyding PLoS Negl Trop Dis Research Article BACKGROUND: Genital granulomas induced by Schistosoma haematobium eggs can manifest as different lesion types visible by colposcopy; rubbery papules (RP), homogenous sandy patches (HSP) and grainy sandy patches (GSP). Pronounced tissue eosinophilia is a candidate marker for active S. haematobium pathology, as viable schistosome egg granulomas often are eosinophil rich. Here it was investigated whether eosinophil granule proteins ECP (eosinophil cationic protein) and EPX (eosinophil protein-X) in urine and genital lavage can be used as markers for active FGS lesions. METHODS: Uro-genital samples from 118 Malagasy women were analysed for ECP and EPX by standard sandwich avidin/biotin amplified ELISA. PRINCIPAL FINDINGS: The women with RP lesions had significantly higher levels of ECP and EPX in both lavage and urine. Furthermore, women with RP lesions were significantly younger than those with GSP. This could indicate that RP lesions might be more recently established and thus represent an earlier inflammatory lesion stage. CONCLUSION: ECP in genital lavage might be a future tool aiding the identification of FGS pathology at a stage where reversibility remains a possibility following praziquantel treatment. Public Library of Science 2014-07-17 /pmc/articles/PMC4102437/ /pubmed/25033206 http://dx.doi.org/10.1371/journal.pntd.0002974 Text en © 2014 Ramarokoto et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ramarokoto, Charles Emile
Kildemoes, Anna Overgaard
Randrianasolo, Bodo Sahondra
Ravoniarimbinina, Pascaline
Ravaoalimalala, Vololomboahangy Elisabeth
Leutscher, Peter
Kjetland, Eyrun Floerecke
Vennervald, Birgitte Jyding
Eosinophil Granule Proteins ECP and EPX as Markers for a Potential Early-Stage Inflammatory Lesion in Female Genital Schistosomiasis (FGS)
title Eosinophil Granule Proteins ECP and EPX as Markers for a Potential Early-Stage Inflammatory Lesion in Female Genital Schistosomiasis (FGS)
title_full Eosinophil Granule Proteins ECP and EPX as Markers for a Potential Early-Stage Inflammatory Lesion in Female Genital Schistosomiasis (FGS)
title_fullStr Eosinophil Granule Proteins ECP and EPX as Markers for a Potential Early-Stage Inflammatory Lesion in Female Genital Schistosomiasis (FGS)
title_full_unstemmed Eosinophil Granule Proteins ECP and EPX as Markers for a Potential Early-Stage Inflammatory Lesion in Female Genital Schistosomiasis (FGS)
title_short Eosinophil Granule Proteins ECP and EPX as Markers for a Potential Early-Stage Inflammatory Lesion in Female Genital Schistosomiasis (FGS)
title_sort eosinophil granule proteins ecp and epx as markers for a potential early-stage inflammatory lesion in female genital schistosomiasis (fgs)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4102437/
https://www.ncbi.nlm.nih.gov/pubmed/25033206
http://dx.doi.org/10.1371/journal.pntd.0002974
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