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An in vivo culture system for human embryos using an encapsulation technology: a pilot study

Identifieur interne : 000A41 ( Istex/Corpus ); précédent : 000A40; suivant : 000A42

An in vivo culture system for human embryos using an encapsulation technology: a pilot study

Auteurs : C. Blockeel ; P. Mock ; G. Verheyen ; N. Bouche ; Ph. Le Goff ; Y. Heyman ; C. Wrenzycki ; K. Hffmann ; H. Niemann ; P. Haentjens ; M. J. De Los Santos ; M. Fernandez-Sanchez ; M. Velasco ; P. Aebischer ; P. Devroey ; C. Simn

Source :

RBID : ISTEX:033DA12265BEEFC4242E6536902363F8C6BE7EA5

Abstract

BACKGROUND Animal studies have demonstrated better embryo development in vivo than in vitro. This pilot study tested the feasibility of using a novel in utero culture system (IUCS) to obtain normal human fertilization and embryo development. METHODS The IUCS device comprised a perforated silicone hollow tube. The study included 13 patients (<36 years) undergoing a first intracytoplasmic sperm injection (ICSI) treatment and 167 metaphase II oocytes in three groups. In Group 1, 12 h after ICSI, sibling oocytes were assigned to IUCS or conventional in vitro culture. The device was retrieved on Day 1, and all zygotes were cultured in vitro till Day 5. In Group 2, fertilized oocytes were assigned on Day 1, embryos retrieved on Day 3 and all embryos cultured till Day 5. In Group 3, after Day 0 assignment, embryos were retrieved on Day 3 for blastomere biopsy and fluorescence in situ hybridization (FISH) and cultured until Day 5. The highest quality blastocysts were transferred on Day 5. RESULTS Fertilization and embryo development were comparable in the in vitro and IUCS arms, with a tendency towards better embryo quality in the IUCS. FISH analysis in Group 3 revealed more normal embryos using the IUCS (P 0.049). Three clinical pregnancies and live births were obtained: two from the IUCS arm and one from the in vitro arm. CONCLUSIONS Our pilot study shows that this new IUCS appears to be feasible and safe, supporting normal fertilization, embryo development and normal chromosomal segregation. Furthermore, live births are possible after the transient presence of a silicone device in the uterus.Clinicaltrials.gov: NCT00480103.

Url:
DOI: 10.1093/humrep/dep005

Links to Exploration step

ISTEX:033DA12265BEEFC4242E6536902363F8C6BE7EA5

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<div type="abstract">BACKGROUND Animal studies have demonstrated better embryo development in vivo than in vitro. This pilot study tested the feasibility of using a novel in utero culture system (IUCS) to obtain normal human fertilization and embryo development. METHODS The IUCS device comprised a perforated silicone hollow tube. The study included 13 patients (<36 years) undergoing a first intracytoplasmic sperm injection (ICSI) treatment and 167 metaphase II oocytes in three groups. In Group 1, 12 h after ICSI, sibling oocytes were assigned to IUCS or conventional in vitro culture. The device was retrieved on Day 1, and all zygotes were cultured in vitro till Day 5. In Group 2, fertilized oocytes were assigned on Day 1, embryos retrieved on Day 3 and all embryos cultured till Day 5. In Group 3, after Day 0 assignment, embryos were retrieved on Day 3 for blastomere biopsy and fluorescence in situ hybridization (FISH) and cultured until Day 5. The highest quality blastocysts were transferred on Day 5. RESULTS Fertilization and embryo development were comparable in the in vitro and IUCS arms, with a tendency towards better embryo quality in the IUCS. FISH analysis in Group 3 revealed more normal embryos using the IUCS (P 0.049). Three clinical pregnancies and live births were obtained: two from the IUCS arm and one from the in vitro arm. CONCLUSIONS Our pilot study shows that this new IUCS appears to be feasible and safe, supporting normal fertilization, embryo development and normal chromosomal segregation. Furthermore, live births are possible after the transient presence of a silicone device in the uterus.Clinicaltrials.gov: NCT00480103.</div>
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<affiliation>Anecova Inc., Lausanne, Switzerland</affiliation>
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<forename type="first">P.</forename>
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<forename type="first">M.J.</forename>
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<affiliation>Instituto Valenciano de Infertilidad (IVI), Valencia, Spain</affiliation>
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<forename type="first">M.</forename>
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<forename type="first">P.</forename>
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<p>BACKGROUND Animal studies have demonstrated better embryo development in vivo than in vitro. This pilot study tested the feasibility of using a novel in utero culture system (IUCS) to obtain normal human fertilization and embryo development. METHODS The IUCS device comprised a perforated silicone hollow tube. The study included 13 patients (<36 years) undergoing a first intracytoplasmic sperm injection (ICSI) treatment and 167 metaphase II oocytes in three groups. In Group 1, 12 h after ICSI, sibling oocytes were assigned to IUCS or conventional in vitro culture. The device was retrieved on Day 1, and all zygotes were cultured in vitro till Day 5. In Group 2, fertilized oocytes were assigned on Day 1, embryos retrieved on Day 3 and all embryos cultured till Day 5. In Group 3, after Day 0 assignment, embryos were retrieved on Day 3 for blastomere biopsy and fluorescence in situ hybridization (FISH) and cultured until Day 5. The highest quality blastocysts were transferred on Day 5. RESULTS Fertilization and embryo development were comparable in the in vitro and IUCS arms, with a tendency towards better embryo quality in the IUCS. FISH analysis in Group 3 revealed more normal embryos using the IUCS (P 0.049). Three clinical pregnancies and live births were obtained: two from the IUCS arm and one from the in vitro arm. CONCLUSIONS Our pilot study shows that this new IUCS appears to be feasible and safe, supporting normal fertilization, embryo development and normal chromosomal segregation. Furthermore, live births are possible after the transient presence of a silicone device in the uterus.Clinicaltrials.gov: NCT00480103.</p>
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</article-categories>
<title-group>
<article-title>An
<italic>in vivo</italic>
culture system for human embryos using an encapsulation technology: a pilot study</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Blockeel</surname>
<given-names>C.</given-names>
</name>
<xref ref-type="aff" rid="af1">1</xref>
<xref ref-type="author-notes" rid="FN1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mock</surname>
<given-names>P.</given-names>
</name>
<xref ref-type="aff" rid="af2">2</xref>
<xref ref-type="aff" rid="af9">9</xref>
<xref ref-type="author-notes" rid="FN1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Verheyen</surname>
<given-names>G.</given-names>
</name>
<xref ref-type="aff" rid="af1">1</xref>
<xref ref-type="author-notes" rid="FN1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Bouche</surname>
<given-names>N.</given-names>
</name>
<xref ref-type="aff" rid="af2">2</xref>
<xref ref-type="aff" rid="af3">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Le Goff</surname>
<given-names>Ph.</given-names>
</name>
<xref ref-type="aff" rid="af2">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Heyman</surname>
<given-names>Y.</given-names>
</name>
<xref ref-type="aff" rid="af4">4</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Wrenzycki</surname>
<given-names>C.</given-names>
</name>
<xref ref-type="aff" rid="af5">5</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Höffmann</surname>
<given-names>K.</given-names>
</name>
<xref ref-type="aff" rid="af5">5</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Niemann</surname>
<given-names>H.</given-names>
</name>
<xref ref-type="aff" rid="af6">6</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Haentjens</surname>
<given-names>P.</given-names>
</name>
<xref ref-type="aff" rid="af7">7</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>de Los Santos</surname>
<given-names>M.J.</given-names>
</name>
<xref ref-type="aff" rid="af8">8</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Fernandez-Sanchez</surname>
<given-names>M.</given-names>
</name>
<xref ref-type="aff" rid="af8">8</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Velasco</surname>
<given-names>M.</given-names>
</name>
<xref ref-type="aff" rid="af2">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Aebischer</surname>
<given-names>P.</given-names>
</name>
<xref ref-type="aff" rid="af3">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Devroey</surname>
<given-names>P.</given-names>
</name>
<xref ref-type="aff" rid="af1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Simón</surname>
<given-names>C.</given-names>
</name>
<xref ref-type="aff" rid="af8">8</xref>
<xref ref-type="corresp" rid="cor1">10</xref>
</contrib>
</contrib-group>
<aff id="af1">
<label>1</label>
<institution>Centre for Reproductive Medicine</institution>
,
<addr-line>UZ Brussel, Brussels</addr-line>
,
<country>Belgium</country>
</aff>
<aff id="af2">
<label>2</label>
<institution>Anecova Inc.</institution>
,
<addr-line>Lausanne</addr-line>
,
<country>Switzerland</country>
</aff>
<aff id="af3">
<label>3</label>
<institution>Brain and Mind Institute, Ecole Polytechnique Fédérale de Lausanne, EPFL</institution>
,
<addr-line>Lausanne</addr-line>
,
<country>Switzerland</country>
</aff>
<aff id="af4">
<label>4</label>
<institution>Institut National de Recherche Agronomique, INRA</institution>
,
<addr-line>Jouy en Josas</addr-line>
,
<country>France</country>
</aff>
<aff id="af5">
<label>5</label>
<addr-line>Stiftung Tierärztliche Hochschule, Klinik für Rinder</addr-line>
,
<institution>Reproduktionsmedizinische Einheit der Kliniken</institution>
,
<addr-line>Hannover</addr-line>
,
<country>Germany</country>
</aff>
<aff id="af6">
<label>6</label>
<institution>Institut für Nutztiergenetik, FLI, Mariensee</institution>
,
<addr-line>Neustadt</addr-line>
,
<country>Germany</country>
</aff>
<aff id="af7">
<label>7</label>
<institution>Centre for Outcomes Research and Laboratory for Experimental Surgery</institution>
,
<addr-line>UZ Brussel, Brussels</addr-line>
,
<country>Belgium</country>
</aff>
<aff id="af8">
<label>8</label>
<institution>Instituto Valenciano de Infertilidad (IVI)</institution>
,
<addr-line>Valencia</addr-line>
,
<country>Spain</country>
</aff>
<aff id="af9">
<label>9</label>
<institution>University of Geneva</institution>
,
<addr-line>Geneva</addr-line>
,
<country>Switzerland</country>
</aff>
<author-notes>
<fn id="FN1">
<label></label>
<p>The first three authors have contributed equally.</p>
</fn>
<corresp id="cor1">
<label>10</label>
Corresponding address.
<institution>Fundación del Instituto Valenciano de Infertilidad (FIVI), University of Valencia</institution>
,
<addr-line>C/Guadassuar, 1, 46015 Valencia</addr-line>
,
<country>Spain</country>
. Tel:
<phone>+34-96-345-55-60</phone>
; Fax:
<fax>+34-96-345-55-12;</fax>
E-mail:
<email>csimon@ivi.es</email>
</corresp>
</author-notes>
<pub-date pub-type="ppub">
<month>4</month>
<year>2009</year>
</pub-date>
<pub-date pub-type="epub">
<day>10</day>
<month>3</month>
<year>2009</year>
</pub-date>
<volume>24</volume>
<issue>4</issue>
<fpage>790</fpage>
<lpage>796</lpage>
<history>
<date date-type="received">
<day>2</day>
<month>6</month>
<year>2008</year>
</date>
<date date-type="rev-recd">
<day>16</day>
<month>12</month>
<year>2008</year>
</date>
<date date-type="accepted">
<day>28</day>
<month>12</month>
<year>2008</year>
</date>
</history>
<copyright-statement>© The Author 2009. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org</copyright-statement>
<copyright-year>2009</copyright-year>
<license license-type="creative-commons" xlink:href="http://creativecommons.org/licenses/by-nc/2.0/uk/">
<p>The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed: the Journal and Oxford University Press are attributed as the original place of publication with the correct citation details given: if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative word this must be clearly indicated. For commercial re-use, please contact journals.permissions@oxfordjournals.org</p>
</license>
<abstract>
<sec>
<title>BACKGROUND</title>
<p>Animal studies have demonstrated better embryo development
<italic>in vivo</italic>
than
<italic>in vitro</italic>
. This pilot study tested the feasibility of using a novel
<italic>in utero</italic>
culture system (IUCS) to obtain normal human fertilization and embryo development.</p>
</sec>
<sec>
<title>METHODS</title>
<p>The IUCS device comprised a perforated silicone hollow tube. The study included 13 patients (<36 years) undergoing a first intracytoplasmic sperm injection (ICSI) treatment and 167 metaphase II oocytes in three groups. In Group 1, 1–2 h after ICSI, sibling oocytes were assigned to IUCS or conventional
<italic>in vitro</italic>
culture. The device was retrieved on Day 1, and all zygotes were cultured
<italic>in vitro</italic>
till Day 5. In Group 2, fertilized oocytes were assigned on Day 1, embryos retrieved on Day 3 and all embryos cultured till Day 5. In Group 3, after Day 0 assignment, embryos were retrieved on Day 3 for blastomere biopsy and fluorescence
<italic>in situ</italic>
hybridization (FISH) and cultured until Day 5. The highest quality blastocysts were transferred on Day 5.</p>
</sec>
<sec>
<title>RESULTS</title>
<p>Fertilization and embryo development were comparable in the
<italic>in vitro</italic>
and IUCS arms, with a tendency towards better embryo quality in the IUCS. FISH analysis in Group 3 revealed more normal embryos using the IUCS (
<italic>P</italic>
= 0.049). Three clinical pregnancies and live births were obtained: two from the IUCS arm and one from the
<italic>in vitro</italic>
arm.</p>
</sec>
<sec>
<title>CONCLUSIONS</title>
<p>Our pilot study shows that this new IUCS appears to be feasible and safe, supporting normal fertilization, embryo development and normal chromosomal segregation. Furthermore, live births are possible after the transient presence of a silicone device in the uterus.Clinicaltrials.gov: NCT00480103.</p>
</sec>
</abstract>
<kwd-group>
<title>Keywords</title>
<kwd>
<italic>in vivo</italic>
culture</kwd>
<kwd>
<italic>in utero</italic>
culture system</kwd>
<kwd>ICSI</kwd>
<kwd>embryos</kwd>
<kwd>oocytes</kwd>
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<namePart type="family">Velasco</namePart>
<affiliation>Anecova Inc., Lausanne, Switzerland</affiliation>
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<name type="personal">
<namePart type="given">P.</namePart>
<namePart type="family">Aebischer</namePart>
<affiliation>Brain and Mind Institute, Ecole Polytechnique Fdrale de Lausanne, EPFL, Lausanne, Switzerland</affiliation>
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<name type="personal">
<namePart type="given">P.</namePart>
<namePart type="family">Devroey</namePart>
<affiliation>Centre for Reproductive Medicine, UZ Brussel, Brussels, Belgium</affiliation>
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<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">C.</namePart>
<namePart type="family">Simn</namePart>
<affiliation>Instituto Valenciano de Infertilidad (IVI), Valencia, Spain</affiliation>
<affiliation>E-mail: csimon@ivi.es</affiliation>
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<dateIssued encoding="w3cdtf">2009-04</dateIssued>
<dateCreated encoding="w3cdtf">2009-03-10</dateCreated>
<copyrightDate encoding="w3cdtf">2009</copyrightDate>
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<abstract>BACKGROUND Animal studies have demonstrated better embryo development in vivo than in vitro. This pilot study tested the feasibility of using a novel in utero culture system (IUCS) to obtain normal human fertilization and embryo development. METHODS The IUCS device comprised a perforated silicone hollow tube. The study included 13 patients (<36 years) undergoing a first intracytoplasmic sperm injection (ICSI) treatment and 167 metaphase II oocytes in three groups. In Group 1, 12 h after ICSI, sibling oocytes were assigned to IUCS or conventional in vitro culture. The device was retrieved on Day 1, and all zygotes were cultured in vitro till Day 5. In Group 2, fertilized oocytes were assigned on Day 1, embryos retrieved on Day 3 and all embryos cultured till Day 5. In Group 3, after Day 0 assignment, embryos were retrieved on Day 3 for blastomere biopsy and fluorescence in situ hybridization (FISH) and cultured until Day 5. The highest quality blastocysts were transferred on Day 5. RESULTS Fertilization and embryo development were comparable in the in vitro and IUCS arms, with a tendency towards better embryo quality in the IUCS. FISH analysis in Group 3 revealed more normal embryos using the IUCS (P 0.049). Three clinical pregnancies and live births were obtained: two from the IUCS arm and one from the in vitro arm. CONCLUSIONS Our pilot study shows that this new IUCS appears to be feasible and safe, supporting normal fertilization, embryo development and normal chromosomal segregation. Furthermore, live births are possible after the transient presence of a silicone device in the uterus.Clinicaltrials.gov: NCT00480103.</abstract>
<note type="footnotes">The first three authors have contributed equally.</note>
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<genre>Keywords</genre>
<topic>in vivo culture</topic>
<topic>in utero culture system</topic>
<topic>ICSI</topic>
<topic>embryos</topic>
<topic>oocytes</topic>
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<title>Human Reproduction</title>
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<genre type="journal">journal</genre>
<identifier type="ISSN">0268-1161</identifier>
<identifier type="eISSN">1460-2350</identifier>
<identifier type="PublisherID">humrep</identifier>
<identifier type="PublisherID-hwp">humrep</identifier>
<part>
<date>2009</date>
<detail type="volume">
<caption>vol.</caption>
<number>24</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>4</number>
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<start>790</start>
<end>796</end>
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<accessCondition type="use and reproduction" contentType="copyright">The Author 2009. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissionsoxfordjournals.org</accessCondition>
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