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Immunological profiling of molecularly classified high-risk endometrial cancers identifies POLE-mutant and microsatellite unstable carcinomas as candidates for checkpoint inhibition

Identifieur interne : 000854 ( Pmc/Checkpoint ); précédent : 000853; suivant : 000855

Immunological profiling of molecularly classified high-risk endometrial cancers identifies POLE-mutant and microsatellite unstable carcinomas as candidates for checkpoint inhibition

Auteurs : Florine A. Eggink ; Inge C. Van Gool ; Alexandra Leary [France] ; Pamela M. Pollock [Australie] ; Emma J. Crosbie [Royaume-Uni] ; Linda Mileshkin [Australie] ; Ekaterina S. Jordanova ; Julien Adam [France] ; Luke Freeman-Mills [Royaume-Uni] ; David N. Church [Royaume-Uni] ; Carien L. Creutzberg ; Marco De Bruyn ; Hans W. Nijman ; Tjalling Bosse

Source :

RBID : PMC:5353925

Abstract

ABSTRACT

High-risk endometrial cancer (EC) is an aggressive disease for which new therapeutic options are needed. Aims of this study were to validate the enhanced immune response in highly mutated ECs and to explore immune profiles in other EC subgroups. We evaluated immune infiltration in 116 high-risk ECs from the TransPORTEC consortium, previously classified into four molecular subtypes: (i) ultramutated POLE exonuclease domain-mutant ECs (POLE-mutant); (ii) hypermutated microsatellite unstable (MSI); (iii) p53-mutant; and (iv) no specific molecular profile (NSMP). Within The Cancer Genome Atlas (TCGA) EC cohort, significantly higher numbers of predicted neoantigens were demonstrated in POLE-mutant and MSI tumors compared with NSMP and p53-mutants. This was reflected by enhanced immune expression and infiltration in POLE-mutant and MSI tumors in both the TCGA cohort (mRNA expression) and the TransPORTEC cohort (immunohistochemistry) with high infiltration of CD8+ (90% and 69%), PD-1+ (73% and 69%) and PD-L1+ immune cells (100% and 71%). Notably, a subset of p53-mutant and NSMP cancers was characterized by signs of an antitumor immune response (43% and 31% of tumors with high infiltration of CD8+ cells, respectively), despite a low number of predicted neoantigens. In conclusion, the presence of enhanced immune infiltration, particularly high numbers of PD-1 and PD-L1 positive cells, in highly mutated, neoantigen-rich POLE-mutant and MSI endometrial tumors suggests sensitivity to immune checkpoint inhibitors.


Url:
DOI: 10.1080/2162402X.2016.1264565
PubMed: 28344870
PubMed Central: 5353925


Affiliations:


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PMC:5353925

Le document en format XML

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<title xml:lang="en" level="a" type="main">Immunological profiling of molecularly classified high-risk endometrial cancers identifies
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<name sortKey="Leary, Alexandra" sort="Leary, Alexandra" uniqKey="Leary A" first="Alexandra" last="Leary">Alexandra Leary</name>
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, Brisbane, QLD,
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</nlm:aff>
<country xml:lang="fr">Australie</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
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<name sortKey="Crosbie, Emma J" sort="Crosbie, Emma J" uniqKey="Crosbie E" first="Emma J." last="Crosbie">Emma J. Crosbie</name>
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, Manchester,
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</nlm:aff>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
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<name sortKey="Mileshkin, Linda" sort="Mileshkin, Linda" uniqKey="Mileshkin L" first="Linda" last="Mileshkin">Linda Mileshkin</name>
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, East Melbourne, VIC,
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</nlm:aff>
<country xml:lang="fr">Australie</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
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<name sortKey="Jordanova, Ekaterina S" sort="Jordanova, Ekaterina S" uniqKey="Jordanova E" first="Ekaterina S." last="Jordanova">Ekaterina S. Jordanova</name>
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, Leiden,
<country>the Netherlands</country>
</nlm:aff>
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<affiliation>
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, Amsterdam,
<country>the Netherlands</country>
</nlm:aff>
<wicri:noCountry code="nlm country">the Netherlands</wicri:noCountry>
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<name sortKey="Adam, Julien" sort="Adam, Julien" uniqKey="Adam J" first="Julien" last="Adam">Julien Adam</name>
<affiliation wicri:level="1">
<nlm:aff id="af0003">
<institution>Department of Medical Oncology, INSERM U981, Gustave Roussy Cancer Center</institution>
, Villejuif,
<country>France</country>
</nlm:aff>
<country xml:lang="fr">France</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
</affiliation>
</author>
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<name sortKey="Freeman Mills, Luke" sort="Freeman Mills, Luke" uniqKey="Freeman Mills L" first="Luke" last="Freeman-Mills">Luke Freeman-Mills</name>
<affiliation wicri:level="1">
<nlm:aff id="af0008">
<institution>Tumour Genomics and Immunology Group, Oxford Centre for Cancer Gene Research, The Wellcome Trust Centre for Human Genetics, University of Oxford</institution>
, Oxford,
<country>UK</country>
</nlm:aff>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
</affiliation>
</author>
<author>
<name sortKey="Church, David N" sort="Church, David N" uniqKey="Church D" first="David N." last="Church">David N. Church</name>
<affiliation wicri:level="1">
<nlm:aff id="af0008">
<institution>Tumour Genomics and Immunology Group, Oxford Centre for Cancer Gene Research, The Wellcome Trust Centre for Human Genetics, University of Oxford</institution>
, Oxford,
<country>UK</country>
</nlm:aff>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
</affiliation>
<affiliation wicri:level="1">
<nlm:aff id="af0009">
<institution>Oxford Cancer Centre, Churchill Hospital</institution>
, Oxford,
<country>UK</country>
</nlm:aff>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
</affiliation>
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<name sortKey="Creutzberg, Carien L" sort="Creutzberg, Carien L" uniqKey="Creutzberg C" first="Carien L." last="Creutzberg">Carien L. Creutzberg</name>
<affiliation>
<nlm:aff id="af0010">
<institution>Department of Clinical Oncology, Leiden University Medical Center</institution>
, Leiden,
<country>the Netherlands</country>
</nlm:aff>
<wicri:noCountry code="nlm country">the Netherlands</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="De Bruyn, Marco" sort="De Bruyn, Marco" uniqKey="De Bruyn M" first="Marco" last="De Bruyn">Marco De Bruyn</name>
<affiliation>
<nlm:aff id="af0001">
<institution>Department of Obstetrics and Gynecology, University of Groningen, University Medical Center Groningen</institution>
, Groningen,
<country>the Netherlands</country>
</nlm:aff>
<wicri:noCountry code="nlm country">the Netherlands</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="Nijman, Hans W" sort="Nijman, Hans W" uniqKey="Nijman H" first="Hans W." last="Nijman">Hans W. Nijman</name>
<affiliation>
<nlm:aff id="af0001">
<institution>Department of Obstetrics and Gynecology, University of Groningen, University Medical Center Groningen</institution>
, Groningen,
<country>the Netherlands</country>
</nlm:aff>
<wicri:noCountry code="nlm country">the Netherlands</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="Bosse, Tjalling" sort="Bosse, Tjalling" uniqKey="Bosse T" first="Tjalling" last="Bosse">Tjalling Bosse</name>
<affiliation>
<nlm:aff id="af0002">
<institution>Department of Pathology, Leiden University Medical Center</institution>
, Leiden,
<country>the Netherlands</country>
</nlm:aff>
<wicri:noCountry code="nlm country">the Netherlands</wicri:noCountry>
</affiliation>
</author>
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<title level="j">Oncoimmunology</title>
<idno type="ISSN">2162-4011</idno>
<idno type="eISSN">2162-402X</idno>
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<date when="2016">2016</date>
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<div type="abstract" xml:lang="en">
<title>ABSTRACT</title>
<p>High-risk endometrial cancer (EC) is an aggressive disease for which new therapeutic options are needed. Aims of this study were to validate the enhanced immune response in highly mutated ECs and to explore immune profiles in other EC subgroups. We evaluated immune infiltration in 116 high-risk ECs from the TransPORTEC consortium, previously classified into four molecular subtypes: (i) ultramutated
<italic>POLE</italic>
exonuclease domain-mutant ECs (
<italic>POLE</italic>
-mutant); (ii) hypermutated microsatellite unstable (MSI); (iii) p53-mutant; and (iv) no specific molecular profile (NSMP). Within The Cancer Genome Atlas (TCGA) EC cohort, significantly higher numbers of predicted neoantigens were demonstrated in
<italic>POLE</italic>
-mutant and MSI tumors compared with NSMP and p53-mutants. This was reflected by enhanced immune expression and infiltration in
<italic>POLE</italic>
-mutant and MSI tumors in both the TCGA cohort (mRNA expression) and the TransPORTEC cohort (immunohistochemistry) with high infiltration of CD8
<sup>+</sup>
(90% and 69%), PD-1
<sup>+</sup>
(73% and 69%) and PD-L1
<sup>+</sup>
immune cells (100% and 71%). Notably, a subset of p53-mutant and NSMP cancers was characterized by signs of an antitumor immune response (43% and 31% of tumors with high infiltration of CD8
<sup>+</sup>
cells, respectively), despite a low number of predicted neoantigens. In conclusion, the presence of enhanced immune infiltration, particularly high numbers of PD-1 and PD-L1 positive cells, in highly mutated, neoantigen-rich
<italic>POLE</italic>
-mutant and MSI endometrial tumors suggests sensitivity to immune checkpoint inhibitors.</p>
</div>
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</TEI>
<pmc article-type="research-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Oncoimmunology</journal-id>
<journal-id journal-id-type="iso-abbrev">Oncoimmunology</journal-id>
<journal-id journal-id-type="publisher-id">KONI</journal-id>
<journal-id journal-id-type="publisher-id">koni20</journal-id>
<journal-title-group>
<journal-title>Oncoimmunology</journal-title>
</journal-title-group>
<issn pub-type="ppub">2162-4011</issn>
<issn pub-type="epub">2162-402X</issn>
<publisher>
<publisher-name>Taylor & Francis</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">28344870</article-id>
<article-id pub-id-type="pmc">5353925</article-id>
<article-id pub-id-type="publisher-id">1264565</article-id>
<article-id pub-id-type="doi">10.1080/2162402X.2016.1264565</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Original Research</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Immunological profiling of molecularly classified high-risk endometrial cancers identifies
<italic>POLE</italic>
-mutant and microsatellite unstable carcinomas as candidates for checkpoint inhibition</article-title>
<alt-title alt-title-type="running-authors">F. A. EGGINK ET AL.</alt-title>
<alt-title alt-title-type="running-title">ONCOIMMUNOLOGY</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Eggink</surname>
<given-names>Florine A.</given-names>
</name>
<xref ref-type="aff" rid="af0001">
<sup>a</sup>
</xref>
<xref ref-type="author-notes" rid="afn0001">
<sup>*</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Van Gool</surname>
<given-names>Inge C.</given-names>
</name>
<xref ref-type="aff" rid="af0002">
<sup>b</sup>
</xref>
<xref ref-type="author-notes" rid="afn0001">
<sup>*</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Leary</surname>
<given-names>Alexandra</given-names>
</name>
<xref ref-type="aff" rid="af0003">
<sup>c</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Pollock</surname>
<given-names>Pamela M.</given-names>
</name>
<xref ref-type="aff" rid="af0004">
<sup>d</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Crosbie</surname>
<given-names>Emma J.</given-names>
</name>
<xref ref-type="aff" rid="af0005">
<sup>e</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mileshkin</surname>
<given-names>Linda</given-names>
</name>
<xref ref-type="aff" rid="af0006">
<sup>f</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Jordanova</surname>
<given-names>Ekaterina S.</given-names>
</name>
<xref ref-type="aff" rid="af0002">
<sup>b</sup>
</xref>
<xref ref-type="aff" rid="af0007">
<sup>g</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Adam</surname>
<given-names>Julien</given-names>
</name>
<xref ref-type="aff" rid="af0003">
<sup>c</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Freeman-Mills</surname>
<given-names>Luke</given-names>
</name>
<xref ref-type="aff" rid="af0008">
<sup>h</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Church</surname>
<given-names>David N.</given-names>
</name>
<xref ref-type="aff" rid="af0008">
<sup>h</sup>
</xref>
<xref ref-type="aff" rid="af0009">
<sup>i</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Creutzberg</surname>
<given-names>Carien L.</given-names>
</name>
<xref ref-type="aff" rid="af0010">
<sup>j</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>De Bruyn</surname>
<given-names>Marco</given-names>
</name>
<xref ref-type="aff" rid="af0001">
<sup>a</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="ORCID">0000-0002-1821-3042</contrib-id>
<name>
<surname>Nijman</surname>
<given-names>Hans W.</given-names>
</name>
<xref ref-type="aff" rid="af0001">
<sup>a</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Bosse</surname>
<given-names>Tjalling</given-names>
</name>
<xref ref-type="aff" rid="af0002">
<sup>b</sup>
</xref>
<xref ref-type="corresp" rid="an0001"></xref>
</contrib>
<aff id="af0001">
<label>a</label>
<institution>Department of Obstetrics and Gynecology, University of Groningen, University Medical Center Groningen</institution>
, Groningen,
<country>the Netherlands</country>
</aff>
<aff id="af0002">
<label>b</label>
<institution>Department of Pathology, Leiden University Medical Center</institution>
, Leiden,
<country>the Netherlands</country>
</aff>
<aff id="af0003">
<label>c</label>
<institution>Department of Medical Oncology, INSERM U981, Gustave Roussy Cancer Center</institution>
, Villejuif,
<country>France</country>
</aff>
<aff id="af0004">
<label>d</label>
<institution>Queensland University of Technology (QUT), Translational Research Institute</institution>
, Brisbane, QLD,
<country>Australia</country>
</aff>
<aff id="af0005">
<label>e</label>
<institution>Institute of Cancer Sciences, University of Manchester, St Marys Hospital</institution>
, Manchester,
<country>UK</country>
</aff>
<aff id="af0006">
<label>f</label>
<institution>Division of Cancer Medicine, Peter MacCallum Cancer Centre</institution>
, East Melbourne, VIC,
<country>Australia</country>
</aff>
<aff id="af0007">
<label>g</label>
<institution>Center for Gynecological Oncology Amsterdam, VU Medical Center</institution>
, Amsterdam,
<country>the Netherlands</country>
</aff>
<aff id="af0008">
<label>h</label>
<institution>Tumour Genomics and Immunology Group, Oxford Centre for Cancer Gene Research, The Wellcome Trust Centre for Human Genetics, University of Oxford</institution>
, Oxford,
<country>UK</country>
</aff>
<aff id="af0009">
<label>i</label>
<institution>Oxford Cancer Centre, Churchill Hospital</institution>
, Oxford,
<country>UK</country>
</aff>
<aff id="af0010">
<label>j</label>
<institution>Department of Clinical Oncology, Leiden University Medical Center</institution>
, Leiden,
<country>the Netherlands</country>
</aff>
</contrib-group>
<author-notes>
<corresp id="an0001">
<bold>CONTACT</bold>
Tjalling Bosse
<email xlink:href="T.Bosse@lumc.nl">T.Bosse@lumc.nl</email>
<institution>Department of Pathology, Leiden University Medical Center</institution>
,
<addr-line>PO Box 9600</addr-line>
, 2300 RC Leiden,
<country>the Netherlands</country>
</corresp>
<fn>
<p>Supplemental data for this article can be accessed on the
<ext-link ext-link-type="uri" xlink:href="http://dx.doi.org/10.1080/2162402X.2016.1264565">publisher's website</ext-link>
.</p>
</fn>
<fn id="afn0001">
<label>*</label>
<p>These authors contributed equally to this work.</p>
</fn>
</author-notes>
<pub-date pub-type="collection">
<year>2017</year>
</pub-date>
<pub-date pub-type="epub">
<day>9</day>
<month>12</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="pmc-release">
<day>9</day>
<month>12</month>
<year>2016</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on the . </pmc-comment>
<volume>6</volume>
<issue>2</issue>
<elocation-id seq="10">e1264565</elocation-id>
<history>
<date date-type="received">
<day>12</day>
<month>10</month>
<year>2016</year>
</date>
<date date-type="rev-recd">
<day>16</day>
<month>11</month>
<year>2016</year>
</date>
<date date-type="accepted">
<day>17</day>
<month>11</month>
<year>2016</year>
</date>
</history>
<permissions>
<pmc-comment> © Florine A. Eggink, Inge C. Van Gool, Alexandra Leary, Pamela M. Pollock, Emma J. Crosbie, Linda Mileshkin, Ekaterina S. Jordanova, Julien Adam, Luke Freeman-Mills, David N. Church, Carien L. Creutzberg, Marco De Bruyn, Hans W. Nijman, and Tjalling Bosse </pmc-comment>
<copyright-statement>© 2017 The Author(s). Published with license by Taylor & Francis Group, LLC</copyright-statement>
<copyright-year>2017</copyright-year>
<copyright-holder>The Author(s)</copyright-holder>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/">
<license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution License (
<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0/">http://creativecommons.org/licenses/by/4.0/</ext-link>
), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<self-uri content-type="pdf" xlink:href="koni-06-02-1264565.pdf"></self-uri>
<abstract>
<title>ABSTRACT</title>
<p>High-risk endometrial cancer (EC) is an aggressive disease for which new therapeutic options are needed. Aims of this study were to validate the enhanced immune response in highly mutated ECs and to explore immune profiles in other EC subgroups. We evaluated immune infiltration in 116 high-risk ECs from the TransPORTEC consortium, previously classified into four molecular subtypes: (i) ultramutated
<italic>POLE</italic>
exonuclease domain-mutant ECs (
<italic>POLE</italic>
-mutant); (ii) hypermutated microsatellite unstable (MSI); (iii) p53-mutant; and (iv) no specific molecular profile (NSMP). Within The Cancer Genome Atlas (TCGA) EC cohort, significantly higher numbers of predicted neoantigens were demonstrated in
<italic>POLE</italic>
-mutant and MSI tumors compared with NSMP and p53-mutants. This was reflected by enhanced immune expression and infiltration in
<italic>POLE</italic>
-mutant and MSI tumors in both the TCGA cohort (mRNA expression) and the TransPORTEC cohort (immunohistochemistry) with high infiltration of CD8
<sup>+</sup>
(90% and 69%), PD-1
<sup>+</sup>
(73% and 69%) and PD-L1
<sup>+</sup>
immune cells (100% and 71%). Notably, a subset of p53-mutant and NSMP cancers was characterized by signs of an antitumor immune response (43% and 31% of tumors with high infiltration of CD8
<sup>+</sup>
cells, respectively), despite a low number of predicted neoantigens. In conclusion, the presence of enhanced immune infiltration, particularly high numbers of PD-1 and PD-L1 positive cells, in highly mutated, neoantigen-rich
<italic>POLE</italic>
-mutant and MSI endometrial tumors suggests sensitivity to immune checkpoint inhibitors.</p>
</abstract>
<kwd-group kwd-group-type="author">
<title>KEYWORDS</title>
<kwd>Checkpoint inhibition</kwd>
<kwd>endometrial cancer</kwd>
<kwd>high-risk</kwd>
<kwd>molecular classification</kwd>
<kwd>tumor-infiltrating lymphocytes</kwd>
</kwd-group>
<counts>
<fig-count count="6"></fig-count>
<table-count count="1"></table-count>
<equation-count count="0"></equation-count>
<ref-count count="59"></ref-count>
<page-count count="13"></page-count>
</counts>
</article-meta>
</front>
</pmc>
<affiliations>
<list>
<country>
<li>Australie</li>
<li>France</li>
<li>Royaume-Uni</li>
</country>
</list>
<tree>
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<name sortKey="De Bruyn, Marco" sort="De Bruyn, Marco" uniqKey="De Bruyn M" first="Marco" last="De Bruyn">Marco De Bruyn</name>
<name sortKey="Eggink, Florine A" sort="Eggink, Florine A" uniqKey="Eggink F" first="Florine A." last="Eggink">Florine A. Eggink</name>
<name sortKey="Jordanova, Ekaterina S" sort="Jordanova, Ekaterina S" uniqKey="Jordanova E" first="Ekaterina S." last="Jordanova">Ekaterina S. Jordanova</name>
<name sortKey="Nijman, Hans W" sort="Nijman, Hans W" uniqKey="Nijman H" first="Hans W." last="Nijman">Hans W. Nijman</name>
<name sortKey="Van Gool, Inge C" sort="Van Gool, Inge C" uniqKey="Van Gool I" first="Inge C." last="Van Gool">Inge C. Van Gool</name>
</noCountry>
<country name="France">
<noRegion>
<name sortKey="Leary, Alexandra" sort="Leary, Alexandra" uniqKey="Leary A" first="Alexandra" last="Leary">Alexandra Leary</name>
</noRegion>
<name sortKey="Adam, Julien" sort="Adam, Julien" uniqKey="Adam J" first="Julien" last="Adam">Julien Adam</name>
</country>
<country name="Australie">
<noRegion>
<name sortKey="Pollock, Pamela M" sort="Pollock, Pamela M" uniqKey="Pollock P" first="Pamela M." last="Pollock">Pamela M. Pollock</name>
</noRegion>
<name sortKey="Mileshkin, Linda" sort="Mileshkin, Linda" uniqKey="Mileshkin L" first="Linda" last="Mileshkin">Linda Mileshkin</name>
</country>
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<noRegion>
<name sortKey="Crosbie, Emma J" sort="Crosbie, Emma J" uniqKey="Crosbie E" first="Emma J." last="Crosbie">Emma J. Crosbie</name>
</noRegion>
<name sortKey="Church, David N" sort="Church, David N" uniqKey="Church D" first="David N." last="Church">David N. Church</name>
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<name sortKey="Freeman Mills, Luke" sort="Freeman Mills, Luke" uniqKey="Freeman Mills L" first="Luke" last="Freeman-Mills">Luke Freeman-Mills</name>
</country>
</tree>
</affiliations>
</record>

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