Cargando…

Ex-Vivo Uterine Environment (EVE) Therapy Induced Limited Fetal Inflammation in a Premature Lamb Model

INTRODUCTION: Ex-vivo uterine environment (EVE) therapy uses an artificial placenta to provide gas exchange and nutrient delivery to a fetus submerged in an amniotic fluid bath. Development of EVE may allow us to treat very premature neonates without mechanical ventilation. Meanwhile, elevations in...

Descripción completa

Detalles Bibliográficos
Autores principales: Miura, Yuichiro, Saito, Masatoshi, Usuda, Haruo, Woodward, Eleanor, Rittenschober-Böhm, Judith, Kannan, Paranthaman S., Musk, Gabrielle C., Matsuda, Tadashi, Newnham, John P., Kemp, Matthew W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608829/
https://www.ncbi.nlm.nih.gov/pubmed/26473607
http://dx.doi.org/10.1371/journal.pone.0140701
_version_ 1782395727426617344
author Miura, Yuichiro
Saito, Masatoshi
Usuda, Haruo
Woodward, Eleanor
Rittenschober-Böhm, Judith
Kannan, Paranthaman S.
Musk, Gabrielle C.
Matsuda, Tadashi
Newnham, John P.
Kemp, Matthew W.
author_facet Miura, Yuichiro
Saito, Masatoshi
Usuda, Haruo
Woodward, Eleanor
Rittenschober-Böhm, Judith
Kannan, Paranthaman S.
Musk, Gabrielle C.
Matsuda, Tadashi
Newnham, John P.
Kemp, Matthew W.
author_sort Miura, Yuichiro
collection PubMed
description INTRODUCTION: Ex-vivo uterine environment (EVE) therapy uses an artificial placenta to provide gas exchange and nutrient delivery to a fetus submerged in an amniotic fluid bath. Development of EVE may allow us to treat very premature neonates without mechanical ventilation. Meanwhile, elevations in fetal inflammation are associated with adverse neonatal outcomes. In the present study, we analysed fetal survival, inflammation and pulmonary maturation in preterm lambs maintained on EVE therapy using a parallelised umbilical circuit system with a low priming volume. METHODS: Ewes underwent surgical delivery at 115 days of gestation (term is 150 days), and fetuses were transferred to EVE therapy (EVE group; n = 5). Physiological parameters were continuously monitored; fetal blood samples were intermittently obtained to assess wellbeing and targeted to reference range values for 2 days. Age-matched animals (Control group; n = 6) were surgically delivered at 117 days of gestation. Fetal blood and tissue samples were analysed and compared between the two groups. RESULTS: Fetal survival time in the EVE group was 27.0 ± 15.5 (group mean ± SD) hours. Only one fetus completed the pre-determined study period with optimal physiological parameters, while the other 4 animals demonstrated physiological deterioration or death prior to the pre-determined study end point. Significant elevations (p<0.05) in: i) inflammatory proteins in fetal plasma; ii) selected cytokine/chemokine mRNA expression levels in fetal tissues; and iii) histological inflammatory score in fetal lung, were observed in the EVE group compared to the Control group. There was no significant difference (p>0.05) in surfactant protein mRNA expression level between the two groups. CONCLUSION: In this study, we achieved limited fetal survival using EVE therapy. Despite this, EVE therapy only induced a modest fetal inflammatory response and did not promote lung maturation. These data provide additional insight into markers of treatment efficacy for the assessment of future studies.
format Online
Article
Text
id pubmed-4608829
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-46088292015-10-29 Ex-Vivo Uterine Environment (EVE) Therapy Induced Limited Fetal Inflammation in a Premature Lamb Model Miura, Yuichiro Saito, Masatoshi Usuda, Haruo Woodward, Eleanor Rittenschober-Böhm, Judith Kannan, Paranthaman S. Musk, Gabrielle C. Matsuda, Tadashi Newnham, John P. Kemp, Matthew W. PLoS One Research Article INTRODUCTION: Ex-vivo uterine environment (EVE) therapy uses an artificial placenta to provide gas exchange and nutrient delivery to a fetus submerged in an amniotic fluid bath. Development of EVE may allow us to treat very premature neonates without mechanical ventilation. Meanwhile, elevations in fetal inflammation are associated with adverse neonatal outcomes. In the present study, we analysed fetal survival, inflammation and pulmonary maturation in preterm lambs maintained on EVE therapy using a parallelised umbilical circuit system with a low priming volume. METHODS: Ewes underwent surgical delivery at 115 days of gestation (term is 150 days), and fetuses were transferred to EVE therapy (EVE group; n = 5). Physiological parameters were continuously monitored; fetal blood samples were intermittently obtained to assess wellbeing and targeted to reference range values for 2 days. Age-matched animals (Control group; n = 6) were surgically delivered at 117 days of gestation. Fetal blood and tissue samples were analysed and compared between the two groups. RESULTS: Fetal survival time in the EVE group was 27.0 ± 15.5 (group mean ± SD) hours. Only one fetus completed the pre-determined study period with optimal physiological parameters, while the other 4 animals demonstrated physiological deterioration or death prior to the pre-determined study end point. Significant elevations (p<0.05) in: i) inflammatory proteins in fetal plasma; ii) selected cytokine/chemokine mRNA expression levels in fetal tissues; and iii) histological inflammatory score in fetal lung, were observed in the EVE group compared to the Control group. There was no significant difference (p>0.05) in surfactant protein mRNA expression level between the two groups. CONCLUSION: In this study, we achieved limited fetal survival using EVE therapy. Despite this, EVE therapy only induced a modest fetal inflammatory response and did not promote lung maturation. These data provide additional insight into markers of treatment efficacy for the assessment of future studies. Public Library of Science 2015-10-16 /pmc/articles/PMC4608829/ /pubmed/26473607 http://dx.doi.org/10.1371/journal.pone.0140701 Text en © 2015 Miura 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
Miura, Yuichiro
Saito, Masatoshi
Usuda, Haruo
Woodward, Eleanor
Rittenschober-Böhm, Judith
Kannan, Paranthaman S.
Musk, Gabrielle C.
Matsuda, Tadashi
Newnham, John P.
Kemp, Matthew W.
Ex-Vivo Uterine Environment (EVE) Therapy Induced Limited Fetal Inflammation in a Premature Lamb Model
title Ex-Vivo Uterine Environment (EVE) Therapy Induced Limited Fetal Inflammation in a Premature Lamb Model
title_full Ex-Vivo Uterine Environment (EVE) Therapy Induced Limited Fetal Inflammation in a Premature Lamb Model
title_fullStr Ex-Vivo Uterine Environment (EVE) Therapy Induced Limited Fetal Inflammation in a Premature Lamb Model
title_full_unstemmed Ex-Vivo Uterine Environment (EVE) Therapy Induced Limited Fetal Inflammation in a Premature Lamb Model
title_short Ex-Vivo Uterine Environment (EVE) Therapy Induced Limited Fetal Inflammation in a Premature Lamb Model
title_sort ex-vivo uterine environment (eve) therapy induced limited fetal inflammation in a premature lamb model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608829/
https://www.ncbi.nlm.nih.gov/pubmed/26473607
http://dx.doi.org/10.1371/journal.pone.0140701
work_keys_str_mv AT miurayuichiro exvivouterineenvironmentevetherapyinducedlimitedfetalinflammationinaprematurelambmodel
AT saitomasatoshi exvivouterineenvironmentevetherapyinducedlimitedfetalinflammationinaprematurelambmodel
AT usudaharuo exvivouterineenvironmentevetherapyinducedlimitedfetalinflammationinaprematurelambmodel
AT woodwardeleanor exvivouterineenvironmentevetherapyinducedlimitedfetalinflammationinaprematurelambmodel
AT rittenschoberbohmjudith exvivouterineenvironmentevetherapyinducedlimitedfetalinflammationinaprematurelambmodel
AT kannanparanthamans exvivouterineenvironmentevetherapyinducedlimitedfetalinflammationinaprematurelambmodel
AT muskgabriellec exvivouterineenvironmentevetherapyinducedlimitedfetalinflammationinaprematurelambmodel
AT matsudatadashi exvivouterineenvironmentevetherapyinducedlimitedfetalinflammationinaprematurelambmodel
AT newnhamjohnp exvivouterineenvironmentevetherapyinducedlimitedfetalinflammationinaprematurelambmodel
AT kempmattheww exvivouterineenvironmentevetherapyinducedlimitedfetalinflammationinaprematurelambmodel