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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Treprostinil increases the number and angiogenic potential of endothelial progenitor cells in children with pulmonary hypertension</title><author><name sortKey="Smadja, David M" sort="Smadja, David M" uniqKey="Smadja D" first="David M." last="Smadja">David M. Smadja</name><affiliation><nlm:aff id="Aff1">Université Paris Descartes, Paris, France</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2">Inserm Unité 765, Faculté de Pharmacie, and AP-HP, Hôpital Européen Georges Pompidou, Haematology Department, 20 rue leblanc, 75015 Paris, France</nlm:aff></affiliation><affiliation><nlm:aff id="Aff4">Vascular Biology Program, Children’s Hospital, Harvard Medical School, Boston, MA USA</nlm:aff></affiliation></author><author><name sortKey="Mauge, Laetitia" sort="Mauge, Laetitia" uniqKey="Mauge L" first="Laetitia" last="Mauge">Laetitia Mauge</name><affiliation><nlm:aff id="Aff1">Université Paris Descartes, Paris, France</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2">Inserm Unité 765, Faculté de Pharmacie, and AP-HP, Hôpital Européen Georges Pompidou, Haematology Department, 20 rue leblanc, 75015 Paris, France</nlm:aff></affiliation></author><author><name sortKey="Gaussem, Pascale" sort="Gaussem, Pascale" uniqKey="Gaussem P" first="Pascale" last="Gaussem">Pascale Gaussem</name><affiliation><nlm:aff id="Aff1">Université Paris Descartes, Paris, France</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2">Inserm Unité 765, Faculté de Pharmacie, and AP-HP, Hôpital Européen Georges Pompidou, Haematology Department, 20 rue leblanc, 75015 Paris, France</nlm:aff></affiliation></author><author><name sortKey="D Udigier, Clement" sort="D Udigier, Clement" uniqKey="D Udigier C" first="Clément" last="D Udigier">Clément D Udigier</name><affiliation><nlm:aff id="Aff1">Université Paris Descartes, Paris, France</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2">Inserm Unité 765, Faculté de Pharmacie, and AP-HP, Hôpital Européen Georges Pompidou, Haematology Department, 20 rue leblanc, 75015 Paris, France</nlm:aff></affiliation></author><author><name sortKey="Israel Biet, Dominique" sort="Israel Biet, Dominique" uniqKey="Israel Biet D" first="Dominique" last="Israel-Biet">Dominique Israel-Biet</name><affiliation><nlm:aff id="Aff1">Université Paris Descartes, Paris, France</nlm:aff></affiliation><affiliation><nlm:aff id="Aff3">AP-HP, Hôpital Européen Georges Pompidou, Pneumology Department, Paris, France</nlm:aff></affiliation><affiliation><nlm:aff id="Aff5">UPRES EA4068, UFR Biomédicale des Saints Pères, Paris, France</nlm:aff></affiliation></author><author><name sortKey="Celermajer, David S" sort="Celermajer, David S" uniqKey="Celermajer D" first="David S." last="Celermajer">David S. Celermajer</name><affiliation><nlm:aff id="Aff6">Sydney Medical School, University of Sydney, Sydney, NSW 2006 Australia</nlm:aff></affiliation></author><author><name sortKey="Bonnet, Damien" sort="Bonnet, Damien" uniqKey="Bonnet D" first="Damien" last="Bonnet">Damien Bonnet</name><affiliation><nlm:aff id="Aff1">Université Paris Descartes, Paris, France</nlm:aff></affiliation><affiliation><nlm:aff id="Aff7">AP-HP, Hôpital Necker-Enfants Malades, Paris, France</nlm:aff></affiliation></author><author><name sortKey="Levy, Marilyne" sort="Levy, Marilyne" uniqKey="Levy M" first="Marilyne" last="Lévy">Marilyne Lévy</name><affiliation><nlm:aff id="Aff1">Université Paris Descartes, Paris, France</nlm:aff></affiliation><affiliation><nlm:aff id="Aff5">UPRES EA4068, UFR Biomédicale des Saints Pères, Paris, France</nlm:aff></affiliation><affiliation><nlm:aff id="Aff7">AP-HP, Hôpital Necker-Enfants Malades, Paris, France</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">21049284</idno><idno type="pmc">3040815</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3040815</idno><idno type="RBID">PMC:3040815</idno><idno type="doi">10.1007/s10456-010-9192-y</idno><date when="2010">2010</date><idno type="wicri:Area/Pmc/Corpus">000A39</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000A39</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Treprostinil increases the number and angiogenic potential of endothelial progenitor cells in children with pulmonary hypertension</title><author><name sortKey="Smadja, David M" sort="Smadja, David M" uniqKey="Smadja D" first="David M." last="Smadja">David M. Smadja</name><affiliation><nlm:aff id="Aff1">Université Paris Descartes, Paris, France</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2">Inserm Unité 765, Faculté de Pharmacie, and AP-HP, Hôpital Européen Georges Pompidou, Haematology Department, 20 rue leblanc, 75015 Paris, France</nlm:aff></affiliation><affiliation><nlm:aff id="Aff4">Vascular Biology Program, Children’s Hospital, Harvard Medical School, Boston, MA USA</nlm:aff></affiliation></author><author><name sortKey="Mauge, Laetitia" sort="Mauge, Laetitia" uniqKey="Mauge L" first="Laetitia" last="Mauge">Laetitia Mauge</name><affiliation><nlm:aff id="Aff1">Université Paris Descartes, Paris, France</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2">Inserm Unité 765, Faculté de Pharmacie, and AP-HP, Hôpital Européen Georges Pompidou, Haematology Department, 20 rue leblanc, 75015 Paris, France</nlm:aff></affiliation></author><author><name sortKey="Gaussem, Pascale" sort="Gaussem, Pascale" uniqKey="Gaussem P" first="Pascale" last="Gaussem">Pascale Gaussem</name><affiliation><nlm:aff id="Aff1">Université Paris Descartes, Paris, France</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2">Inserm Unité 765, Faculté de Pharmacie, and AP-HP, Hôpital Européen Georges Pompidou, Haematology Department, 20 rue leblanc, 75015 Paris, France</nlm:aff></affiliation></author><author><name sortKey="D Udigier, Clement" sort="D Udigier, Clement" uniqKey="D Udigier C" first="Clément" last="D Udigier">Clément D Udigier</name><affiliation><nlm:aff id="Aff1">Université Paris Descartes, Paris, France</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2">Inserm Unité 765, Faculté de Pharmacie, and AP-HP, Hôpital Européen Georges Pompidou, Haematology Department, 20 rue leblanc, 75015 Paris, France</nlm:aff></affiliation></author><author><name sortKey="Israel Biet, Dominique" sort="Israel Biet, Dominique" uniqKey="Israel Biet D" first="Dominique" last="Israel-Biet">Dominique Israel-Biet</name><affiliation><nlm:aff id="Aff1">Université Paris Descartes, Paris, France</nlm:aff></affiliation><affiliation><nlm:aff id="Aff3">AP-HP, Hôpital Européen Georges Pompidou, Pneumology Department, Paris, France</nlm:aff></affiliation><affiliation><nlm:aff id="Aff5">UPRES EA4068, UFR Biomédicale des Saints Pères, Paris, France</nlm:aff></affiliation></author><author><name sortKey="Celermajer, David S" sort="Celermajer, David S" uniqKey="Celermajer D" first="David S." last="Celermajer">David S. Celermajer</name><affiliation><nlm:aff id="Aff6">Sydney Medical School, University of Sydney, Sydney, NSW 2006 Australia</nlm:aff></affiliation></author><author><name sortKey="Bonnet, Damien" sort="Bonnet, Damien" uniqKey="Bonnet D" first="Damien" last="Bonnet">Damien Bonnet</name><affiliation><nlm:aff id="Aff1">Université Paris Descartes, Paris, France</nlm:aff></affiliation><affiliation><nlm:aff id="Aff7">AP-HP, Hôpital Necker-Enfants Malades, Paris, France</nlm:aff></affiliation></author><author><name sortKey="Levy, Marilyne" sort="Levy, Marilyne" uniqKey="Levy M" first="Marilyne" last="Lévy">Marilyne Lévy</name><affiliation><nlm:aff id="Aff1">Université Paris Descartes, Paris, France</nlm:aff></affiliation><affiliation><nlm:aff id="Aff5">UPRES EA4068, UFR Biomédicale des Saints Pères, Paris, France</nlm:aff></affiliation><affiliation><nlm:aff id="Aff7">AP-HP, Hôpital Necker-Enfants Malades, Paris, France</nlm:aff></affiliation></author></analytic><series><title level="j">Angiogenesis</title><idno type="ISSN">0969-6970</idno><idno type="eISSN">1573-7209</idno><imprint><date when="2010">2010</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><sec><title>Background</title><p>Pulmonary vasodilators in general and prostacyclin therapy in particular, have markedly improved the outcome of patients with pulmonary arterial hypertension (PAH). As endothelial dysfunction is a key feature of PAH, and as endothelial progenitor cells (EPC) may contribute to vascular repair in PAH, we suspected that prostacyclin therapy might enhance EPC numbers and functions. In the present study, objectives were to determine whether EPC may contribute to vasodilator treatment efficacy in PAH.</p></sec><sec><title>Methods</title><p>We quantified CD34+ cells, CFU-Hill and ECFC (endothelial colony forming cells) in peripheral blood from children with idiopathic PAH (<italic>n</italic> = 27) or PAH secondary to congenital heart disease (<italic>n</italic> = 52). CD34+ were enumerated by flow cytometry, CFU-Hill and ECFC by a culture assay. ECFC grown ex vivo were tested for their angiogenic capacities before and after prostacyclin analog therapy (subcutaneous treprostinil).</p></sec><sec><title>Results</title><p>ECFC counts were significantly enhanced in the 8 children treated with treprostinil, while no change was observed in children receiving oral therapy with endothelin antagonists and/or PDE5 inhibitors. CD34+ cell and CFU-Hill counts were unaffected. ECFC from patients treated with treprostinil had a hyperproliferative phenotype and showed enhanced angiogenic potential in a nude mouse preclinical model of limb ischemia.</p></sec><sec><title>Conclusions</title><p>ECFC may partly mediate the clinical benefits of prostanoids in pulmonary arterial hypertension.</p></sec></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Simonneau, G" uniqKey="Simonneau G">G Simonneau</name></author><author><name sortKey="Robbins, Im" uniqKey="Robbins I">IM Robbins</name></author><author><name sortKey="Beghetti, M" uniqKey="Beghetti M">M Beghetti</name></author><author><name sortKey="Channick, Rn" uniqKey="Channick R">RN Channick</name></author><author><name sortKey="Delcroix, M" uniqKey="Delcroix M">M Delcroix</name></author><author><name sortKey="Denton, Cp" uniqKey="Denton C">CP Denton</name></author><author><name sortKey="Elliott, Cg" uniqKey="Elliott C">CG Elliott</name></author><author><name 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<front><journal-meta><journal-id journal-id-type="nlm-ta">Angiogenesis</journal-id><journal-title-group><journal-title>Angiogenesis</journal-title></journal-title-group><issn pub-type="ppub">0969-6970</issn><issn pub-type="epub">1573-7209</issn><publisher><publisher-name>Springer Netherlands</publisher-name><publisher-loc>Dordrecht</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">21049284</article-id><article-id pub-id-type="pmc">3040815</article-id><article-id pub-id-type="publisher-id">9192</article-id><article-id pub-id-type="doi">10.1007/s10456-010-9192-y</article-id><article-categories><subj-group subj-group-type="heading"><subject>Original Paper</subject></subj-group></article-categories><title-group><article-title>Treprostinil increases the number and angiogenic potential of endothelial progenitor cells in children with pulmonary hypertension</article-title></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name><surname>Smadja</surname><given-names>David M.</given-names></name><address><phone>+33-1-56093933</phone><fax>+33-1-56093393</fax><email>david.smadja@egp.aphp.fr</email></address><xref ref-type="aff" rid="Aff1">1</xref><xref ref-type="aff" rid="Aff2">2</xref><xref ref-type="aff" rid="Aff4">4</xref></contrib><contrib contrib-type="author"><name><surname>Mauge</surname><given-names>Laetitia</given-names></name><xref ref-type="aff" rid="Aff1">1</xref><xref ref-type="aff" rid="Aff2">2</xref></contrib><contrib contrib-type="author"><name><surname>Gaussem</surname><given-names>Pascale</given-names></name><xref ref-type="aff" rid="Aff1">1</xref><xref ref-type="aff" rid="Aff2">2</xref></contrib><contrib contrib-type="author"><name><surname>d’Audigier</surname><given-names>Clément</given-names></name><xref ref-type="aff" rid="Aff1">1</xref><xref ref-type="aff" rid="Aff2">2</xref></contrib><contrib contrib-type="author"><name><surname>Israel-Biet</surname><given-names>Dominique</given-names></name><xref ref-type="aff" rid="Aff1">1</xref><xref ref-type="aff" rid="Aff3">3</xref><xref ref-type="aff" rid="Aff5">5</xref></contrib><contrib contrib-type="author"><name><surname>Celermajer</surname><given-names>David S.</given-names></name><xref ref-type="aff" rid="Aff6">6</xref></contrib><contrib contrib-type="author"><name><surname>Bonnet</surname><given-names>Damien</given-names></name><xref ref-type="aff" rid="Aff1">1</xref><xref ref-type="aff" rid="Aff7">7</xref></contrib><contrib contrib-type="author"><name><surname>Lévy</surname><given-names>Marilyne</given-names></name><xref ref-type="aff" rid="Aff1">1</xref><xref ref-type="aff" rid="Aff5">5</xref><xref ref-type="aff" rid="Aff7">7</xref></contrib><aff id="Aff1"><label>1</label>Université Paris Descartes, Paris, France</aff><aff id="Aff2"><label>2</label>Inserm Unité 765, Faculté de Pharmacie, and AP-HP, Hôpital Européen Georges Pompidou, Haematology Department, 20 rue leblanc, 75015 Paris, France</aff><aff id="Aff3"><label>3</label>AP-HP, Hôpital Européen Georges Pompidou, Pneumology Department, Paris, France</aff><aff id="Aff4"><label>4</label>Vascular Biology Program, Children’s Hospital, Harvard Medical School, Boston, MA USA</aff><aff id="Aff5"><label>5</label>UPRES EA4068, UFR Biomédicale des Saints Pères, Paris, France</aff><aff id="Aff6"><label>6</label>Sydney Medical School, University of Sydney, Sydney, NSW 2006 Australia</aff><aff id="Aff7"><label>7</label>AP-HP, Hôpital Necker-Enfants Malades, Paris, France</aff></contrib-group><pub-date pub-type="epub"><day>4</day><month>11</month><year>2010</year></pub-date><pub-date pub-type="pmc-release"><day>4</day><month>11</month><year>2010</year></pub-date><pub-date pub-type="ppub"><month>3</month><year>2011</year></pub-date><volume>14</volume><issue>1</issue><fpage>17</fpage><lpage>27</lpage><history><date date-type="received"><day>10</day><month>9</month><year>2010</year></date><date date-type="accepted"><day>19</day><month>10</month><year>2010</year></date></history><permissions><copyright-statement>© The Author(s) 2010</copyright-statement></permissions><abstract id="Abs1"><sec><title>Background</title><p>Pulmonary vasodilators in general and prostacyclin therapy in particular, have markedly improved the outcome of patients with pulmonary arterial hypertension (PAH). As endothelial dysfunction is a key feature of PAH, and as endothelial progenitor cells (EPC) may contribute to vascular repair in PAH, we suspected that prostacyclin therapy might enhance EPC numbers and functions. In the present study, objectives were to determine whether EPC may contribute to vasodilator treatment efficacy in PAH.</p></sec><sec><title>Methods</title><p>We quantified CD34+ cells, CFU-Hill and ECFC (endothelial colony forming cells) in peripheral blood from children with idiopathic PAH (<italic>n</italic> = 27) or PAH secondary to congenital heart disease (<italic>n</italic> = 52). CD34+ were enumerated by flow cytometry, CFU-Hill and ECFC by a culture assay. ECFC grown ex vivo were tested for their angiogenic capacities before and after prostacyclin analog therapy (subcutaneous treprostinil).</p></sec><sec><title>Results</title><p>ECFC counts were significantly enhanced in the 8 children treated with treprostinil, while no change was observed in children receiving oral therapy with endothelin antagonists and/or PDE5 inhibitors. CD34+ cell and CFU-Hill counts were unaffected. ECFC from patients treated with treprostinil had a hyperproliferative phenotype and showed enhanced angiogenic potential in a nude mouse preclinical model of limb ischemia.</p></sec><sec><title>Conclusions</title><p>ECFC may partly mediate the clinical benefits of prostanoids in pulmonary arterial hypertension.</p></sec></abstract><kwd-group><title>Keywords</title><kwd>Pulmonary hypertension</kwd><kwd>Congenital heart disease</kwd><kwd>Vasodilator treatment</kwd><kwd>Treprostinil</kwd><kwd>EPC</kwd></kwd-group><custom-meta-group><custom-meta><meta-name>issue-copyright-statement</meta-name><meta-value>© Springer Science+Business Media B.V. 2011</meta-value></custom-meta></custom-meta-group></article-meta></front><body><sec id="Sec1"><title>Introduction</title><p>Pulmonary vascular disease (PVD) can cause pulmonary arterial hypertension (PAH), usually leading to right heart failure and death if left untreated [<xref ref-type="bibr" rid="CR1">1</xref>]. Endothelial cell dysfunction is a hallmark of both idiopathic PAH and PAH secondary to congenital heart disease [<xref ref-type="bibr" rid="CR2">2</xref>–<xref ref-type="bibr" rid="CR4">4</xref>].</p><p>A role of endothelial progenitor cells (EPC) in vascular repair and new vessel formation has been described [<xref ref-type="bibr" rid="CR5">5</xref>–<xref ref-type="bibr" rid="CR7">7</xref>]. EPC mobilized from bone marrow and/or resident locally in the lung, are thought to be important in maintaining vascular homeostasis; and there is a growing interest in the potential therapeutic or diagnostic use of EPC during PAH. Experimental and clinical studies have examined the possible contribution of EPC to the pathogenesis of PAH, but reported EPC counts in patients with pulmonary hypertension have been inconsistent [<xref ref-type="bibr" rid="CR8">8</xref>–<xref ref-type="bibr" rid="CR11">11</xref>]. Several types of EPC are defined, depending on the method used (flow cytometry or culture) and their characteristics. At least two populations of EPC have been described [<xref ref-type="bibr" rid="CR5">5</xref>, <xref ref-type="bibr" rid="CR12">12</xref>]. “Early” EPC are spindle-shaped and express both endothelial and leukocyte markers. Quantification of this cell population, as described by Hill, utilizes a commercial kit that identifies so-called “CFU-Hill” [<xref ref-type="bibr" rid="CR13">13</xref>]. The number of CFU-Hill in peripheral blood has been reported to correlate inversely with cardiovascular risk factors [<xref ref-type="bibr" rid="CR13">13</xref>]. “Late” EPC, also called endothelial colony-forming cells (ECFC) [<xref ref-type="bibr" rid="CR7">7</xref>, <xref ref-type="bibr" rid="CR14">14</xref>], develop after 1–3 weeks of culture and have the characteristics of precursor cells committed to the endothelial lineage. Both EPC subtypes have therapeutic potential but in vivo, cells that merge into neovessels have an ECFC phenotype [<xref ref-type="bibr" rid="CR6">6</xref>, <xref ref-type="bibr" rid="CR7">7</xref>].</p><p>EPC transplantation was recently shown to improve pulmonary hypertension in a rat model [<xref ref-type="bibr" rid="CR15">15</xref>, <xref ref-type="bibr" rid="CR16">16</xref>], while Wang et al. [<xref ref-type="bibr" rid="CR17">17</xref>] found that EPC transplantation improved exercise capacity and pulmonary hemodynamics in patients with idiopathic PAH , and a contemporary open-label, non-randomized pilot trial showed that EPC transplantation led to significant improvements in exercise capacity, New York Heart Association functional class, and pulmonary hemodynamics in children with idiopathic PAH [<xref ref-type="bibr" rid="CR18">18</xref>].</p><p>“Pulmonary vasodilator” therapy has greatly improved the prognosis of patients with PAH [<xref ref-type="bibr" rid="CR19">19</xref>, <xref ref-type="bibr" rid="CR20">20</xref>]. In particular, parenteral prostacyclin improves the outcome of patients with PVD, not only by inducing pulmonary vasodilation but also by altering pulmonary vascular structure and function during long-term administration. Intravenous prostacyclin is currently recommended for patients of all ages with WHO functional class IV disease, and as add-on therapy for patients remaining in class III despite correctly dosed treatment with endothelin-receptor antagonists (ERA) and phosphodiesterase-5 inhibitors (PDE5) [<xref ref-type="bibr" rid="CR19">19</xref>, <xref ref-type="bibr" rid="CR20">20</xref>]. Subcutaneous treprostinil, a parenteral prostanoid, is sometimes preferred to an intravenous prostacyclin in children, especially to avoid the long-term risks associated with chronic intravenous therapy.</p><p>Given the possible relationship between EPC and treatment efficacy, we therefore examined the impact of treprostinil therapy on the number and functional capacity of EPC in children with advanced PAH.</p></sec><sec id="Sec2" sec-type="methods"><title>Patients and methods</title><sec id="Sec3"><title>Study population (Table <xref rid="Tab1" ref-type="table">1</xref>)</title><p>This prospectively designed study was aimed at determining the numbers and functional capacities of EPC before and after vasodilator treatment, and especially after treprostinil therapy. Blood samples were collected during outpatient visits from patients already on single- or dual-agent therapy. In the 8 treprostinil-treated patients, EPC were studied before treatment initiation, 2 and 5 days later and monthly thereafter.<table-wrap id="Tab1"><label>Table 1</label><caption><p>Characteristics of the patients</p></caption><table frame="hsides" rules="groups"><thead><tr><th align="left"></th><th align="left">Reversible PAH (<italic>n</italic> = 28)</th><th align="left">Irreversible PAH (<italic>n</italic> = 22)</th><th align="left">Idiopathic PAH (<italic>n</italic> = 27)</th><th align="left"><italic>P</italic> value reversible versus irreversible PAH</th><th align="left"><italic>P</italic> value reversible versus Idiopathic PAH</th><th align="left"><italic>P</italic> value irreversible versus Idiopathic PAH</th></tr></thead><tbody><tr><td align="left">Age (y)</td><td char="(" align="char">2 (2.7–6.5)</td><td char="(" align="char">8 (6.1–16.4)</td><td char="(" align="char">6 (4.5–8.4)</td><td char="." align="char">0.01*</td><td char="." align="char">0.16</td><td char="." align="char">0.06</td></tr><tr><td align="left">Saturation (%)</td><td char="(" align="char">96 (89.2–95.3)</td><td char="(" align="char">86 (79.8–91.3)</td><td char="(" align="char">97.5 (93.5–98.4)</td><td char="." align="char">0.02*</td><td char="." align="char">0.07</td><td char="." align="char">0.0008*</td></tr><tr><td align="left">Mean PAP</td><td char="(" align="char">55 (50–66.2)</td><td char="(" align="char">60 (50.3–66.5)</td><td char="(" align="char">53 (46–56.5)</td><td char="." align="char">0.13</td><td char="." align="char">0.15</td><td char="." align="char">0.95</td></tr></tbody></table><table-wrap-foot><p>Data are expressed as medians and confidence intervals (95%CI). Baseline characteristics were compared with Wilcoxon’s rank sum test for non normally distributed variables (age) and Student’s unpaired test otherwise</p><p>* <italic>P</italic> < 0.05, reversible versus irreversible PAH</p></table-wrap-foot></table-wrap></p><p>The study was approved by the institutional ethics committee of Necker-Enfants Malades hospital, and the parents gave their signed informed consent. Fifty-two consecutive patients with CHD and PAH, and 27 consecutive patients with idiopathic PAH (Table <xref rid="Tab1" ref-type="table">1</xref>) were enrolled between February 2008 and 2010. The 27 patients with idiopathic PAH had a median age of 6 years. Among the patients with CHD, 28 (median age 2 years) had reversible PAH, as defined by normal pulmonary pressure 6 months after surgery, while 24 (median age 8 years) had irreversible PAH, based on persistently elevated pulmonary artery pressure and pulmonary vascular resistance. Children with irreversible PAH were older than children with reversible and idiopathic PAH (<italic>P</italic> = 0.01 and <italic>P</italic> = 0.06, respectively) and had lower oxygen saturation values (<italic>P</italic> = 0.02 and <italic>P</italic> = 0.0008, respectively). Pulmonary artery pressure was similar in the three groups (Table <xref rid="Tab1" ref-type="table">1</xref>). Patients with familial PAH associated with <italic>BMPR2</italic> mutations were not included in this study, because of a possible impact of BMP on EPC angiogenic properties [<xref ref-type="bibr" rid="CR6">6</xref>, <xref ref-type="bibr" rid="CR21">21</xref>, <xref ref-type="bibr" rid="CR22">22</xref>]. Indeed, BMPR2 mutations have been reported to affect both early [<xref ref-type="bibr" rid="CR23">23</xref>] and late EPC, the latter showing a hyperproliferative phenotype and an impaired capacity to form vascular networks [<xref ref-type="bibr" rid="CR22">22</xref>]. Because of adverse effects reported with IV epoprostenol and inhaled prostanoids, subcutaneous treprostinil was used as first-line add-on therapy for 8 young children who deteriorated while receiving combined oral therapy with an endothelin receptor agonist and a PDE5 inhibitor. Three of them had idiopathic PAH and five patients had PAH associated with a congenital heart defect. The decision to add subcutaneous tresprostinil was based on their clinical status (change in functional class), including right ventricular dysfunction (hepatomegaly, increase in tricuspid regurgitation volume, dilation of hepatic veins and the inferior vena cava) in seven patients. Two of them also had syncope. One patient in functional class II had severe complications associated with the central venous line used to deliver epoprostenol. All the patients had right heart catheterization prior to treprostinil treatment. Treprostinil administration was initiated at hospital, through a subcutaneous catheter in the outer leg. All the patients initially received a fixed dose of 1.25 ng/kg/min. The dose was then daily increased by 1.25 ng/kg/min, reaching an average of 20 ng/kg/min at hospital discharge. During treprostinil treatment, site pain was evaluated every 6 h using standard pain scales adapted to age. After hospital discharge the treprostinil dose was adjusted at monthly out-patient visits and reached an average of 40 ng/kg/min. Technical assistance was provided at home by specialized nurses trained in the management of parenteral prostanoid therapy in PAH patients. All patients had experienced a clinical improvement performed, for oldest children by 6MWT, and they all showed an improvement in oxygen saturation and functional status, as they were all in functional class I or II. In five patients who had right heart catheterization after treprostinil, pulmonary arterial pressure did not change but cardiac output increased and pulmonary vascular resistance decreased.</p></sec><sec id="Sec4"><title>Flow cytometric quantification of CD34+ hematopoietic progenitor cells (HPC)</title><p>Circulating CD34+ cells were counted by flow cytometry (FC500 Cytometer; Beckman Coulter, Villepinte, France) after staining of whole blood with a fluorescein isothiocyanate (FITC)-labeled monoclonal mouse antihuman CD45 antibody, a phycoerythrin (PE)-labeled monoclonal mouse antihuman-CD34 antibody, and 7AAD (Stemkit<sup>®</sup>; Beckman Coulter). Absolute numbers of CD34+ cells μl<sup>−1</sup> were determined by using calibration beads, as recommended by the manufacturer.</p></sec><sec id="Sec5"><title>EPC quantification by cell culture</title><p>Blood was diluted 1:1 with PBS, 0.2 M EDTA and overlaid on Histopaque-1077 (Sigma–Aldrich, Saint-Quentin Fallavier, France). Cells were centrifuged at 100<italic>g</italic> for 20 min. Mononuclear cells (MNC) were collected and washed 3 times in PBS, 0.2 M EDTA. CFU-Hill were cultured with the EndoCult<sup>®</sup> Liquid Medium kit (StemCell Technologies, Vancouver, BC, Canada) according to the manufacturer’s instructions. Briefly, MNC were resuspended in complete EndoCult<sup>®</sup> medium and seeded at 5 × 10<sup>6</sup> cells/well in fibronectin-coated tissue culture plates (BD, Becton–Dickinson Biosciences). After 48 h, to obtain CFU-Hill, nonadherent cells were collected and plated in Endocult<sup>®</sup> buffer at 10<sup>6</sup> cells/well in 24-well fibronectin-coated plates. CFU-Hill colonies were counted after another 3 days, as recommended by the manufacturer. As previously described [<xref ref-type="bibr" rid="CR7">7</xref>, <xref ref-type="bibr" rid="CR13">13</xref>, <xref ref-type="bibr" rid="CR24">24</xref>], these cells did not replicate in vitro and gradually disappeared 20 days after plating (Fig. <xref rid="Fig1" ref-type="fig">1</xref>b). To obtain ECFC, adherent cells at 48 h were kept in 6-well fibronectin-coated plates in EGM2 medium (Lonza, Saint-Beauzire, France) composed of endothelial cell basal medium-2 (EBM2), 5% fetal bovine serum (FBS) and growth factors. ECFC appeared between 7 and 30 days of culture and consisted of well-circumscribed cobblestone monolayers (Fig. <xref rid="Fig1" ref-type="fig">1</xref>d). Colonies were counted with an inverted microscope at ×20 magnification. The colonies were then harvested, trypsinized and reseeded in 6-well plates for complementary studies.<fig id="Fig1"><label>Fig. 1</label><caption><p>Basal HPC, CFU-Hill and ECFC counts in the children with PAH. <bold>a</bold> NUMBER of CD34+ hematopoietic progenitor cells (HPC) determined by FACS analysis. HPC is significantly higher in idiopathic PAH group. <bold>b</bold> Representative phase-contrast photomicrograph of CFU-Hill colony obtained with Endocult<sup>®</sup>. Note the central core of rounded cells with spindle-shaped cells sprouting through the periphery. <bold>c</bold> Number of CFU-Hill counted with cell culture Endocult<sup>®</sup> assay. No difference was observed between the different patient groups. <bold>d</bold> Representative phase-contrast photomicrograph of an ECFC colony (mag. ×20). <bold>e</bold> Number of ECFC by cell culture. ECFC is significantly higher in the reversible PAH group</p></caption><graphic xlink:href="10456_2010_9192_Fig1_HTML" id="MO1"></graphic></fig></p></sec><sec id="Sec6"><title>ECFC proliferation assay</title><p>After 16 h of serum and growth-factor privation, ECFC were incubated for 48 h in EBM medium, 5% FBS. Proliferation was examined after 48 h by measuring cell phosphatase activity based on the release of paranitrophenol (pNPP) (Sigma) measured at OD 405 nm (Fluostar optima; BMG labtech, Champigny-sur-Marne, France). Control cells were ECFC from cord blood [<xref ref-type="bibr" rid="CR6">6</xref>, <xref ref-type="bibr" rid="CR25">25</xref>–<xref ref-type="bibr" rid="CR27">27</xref>].</p></sec><sec id="Sec7"><title>In vitro matrigel tube formation assay</title><p>After 16 h of serum and growth-factor privation, ECFC (3 × 10<sup>4</sup> cells/well) were seeded on growth factor-reduced Matrigel (200 μl) (BD Biosciences) in EBM2 medium and cultured for 18 h at 37°C with 5% CO<sub>2</sub>. Capillary-like structures were observed by phase-contrast microscopy and networks formed by ECFC were quantified with Videomet software version 5.4.0.</p></sec><sec id="Sec8"><title>Wound healing assay</title><p>A reproducible circular “wound” was made with a tip in confluent monolayers of ECFC cultured in 12-well plates. The surface area of the wound was measured at ×20 magnification under an inverted microscope, then the medium was removed and the cells were further incubated for 4 or 18 h with EBM, 5% FBS and VEGF 50 ng/ml. Wound repair activity was calculated by expressing the area of the wound after 4 or 18 h of incubation as a percentage of the initial area.</p></sec><sec id="Sec9"><title>ECFC angiogenic potential in a mouse model of hind-limb ischemia</title><p>Nude mice underwent surgery to induce unilateral hindlimb ischemia as described elsewhere [<xref ref-type="bibr" rid="CR6">6</xref>, <xref ref-type="bibr" rid="CR28">28</xref>] and were randomized to receive an intravenous injection of 1 × 10<sup>5</sup> ECFC derived from the two treated patient groups or 1 × 10<sup>5</sup> ECFC derived from cord blood. Two independent groups of 20 mice were realized with, in each experiment, 5 mice injected with PBS, 5 mice with cord blood ECFC, 5 mice with ECFC from patients with oral therapy and 5 mice with ECFC from patients with SC-treprostinil. After 2 weeks, the ischemic/normal limb blood flow ratio was determined with a laser Doppler perfusion imaging system.</p></sec><sec id="Sec10"><title>Statistical analysis</title><p>Baseline characteristics were compared between the groups by using Wilcoxon’s rank sum test for non normally distributed variables and Student’s unpaired test otherwise. Student’s paired t test was used to compare progenitor cells from the same subjects before and after vasodilator treatment. Independent-samples t tests were used to compare late EPC functional capacity in vitro and in mice. StatView or SAS statistical software (Cary, NC 27513, USA) was used for all statistical analyses, and 2-tailed <italic>P</italic> values below 0.05 were considered to denote significant differences.</p></sec></sec><sec id="Sec11"><title>Results</title><sec id="Sec12"><title>HPC, CFU-Hill and ECFC counts before treatment</title><p>We found no difference in HPC counts between patients with reversible and irreversible PAH secondary to CHD [<xref ref-type="bibr" rid="CR29">29</xref>], while HPC counts were significantly higher in patients with idiopathic PAH (Fig. <xref rid="Fig1" ref-type="fig">1</xref>a) (<italic>P</italic> = 0.02 vs. patients with reversible PAH and 0.01 vs. patients with irreversible PAH) in agreement with the data published by Diller et al. [<xref ref-type="bibr" rid="CR10">10</xref>]. CFU-Hill counts after 5 days of culture did not differ across the three patient groups (Fig. <xref rid="Fig1" ref-type="fig">1</xref>c). By contrast, ECFC counts were significantly higher in reversible PAH than in irreversible and idiopathic PAH (Fig. <xref rid="Fig1" ref-type="fig">1</xref>e).</p></sec><sec id="Sec13"><title>ECFC numbers are increased by prostanoid treatment</title><p>No significant change in HPC, CFU-Hill and ECFC were observed when all treated patients versus non treated patients were compared (Fig. <xref rid="Fig2" ref-type="fig">2</xref>a, b, c respectively, with <italic>P</italic> = 0.80, 0.89 and 0.15). Oral treatment (monotherapy or bitherapy) did not modify HPC, CFU-Hill and ECFC counts count (respectively, <italic>P</italic> = 0.52, 0.64 and 0.22, Fig. <xref rid="Fig3" ref-type="fig">3</xref>). No change in HPC or CFU-Hill counts (<italic>P</italic> = 0.76 and <italic>P</italic> = 0.19, respectively, Fig. <xref rid="Fig3" ref-type="fig">3</xref>a, b) were observed after prostanoid therapy (SC treprostinil), while in contrast, this led to a significant increase in ECFC counts (<italic>P</italic> = 0.04, Fig. <xref rid="Fig3" ref-type="fig">3</xref>c).<fig id="Fig2"><label>Fig. 2</label><caption><p>HPC, CFU-Hill and ECFC counts in peripheral venous blood of patients with pulmonary hypertension, with and without treatment. <bold>a</bold> Number of CD34+ hematopoietic progenitor cells (HPC) determined by FACS analysis according to patient group. No difference is observed between the treated and non treated patients (<italic>P</italic> = 0.80). <bold>b</bold> Number of CFU-Hill colonies determined by cell culture according to patient group. No difference is observed between the treated and non treated patients (<italic>P</italic> = 0.89). <bold>c</bold> Number of ECFC determined by cell culture according to patient group. No difference is observed between the treated and non treated patients (<italic>P</italic> = 0.15)</p></caption><graphic xlink:href="10456_2010_9192_Fig2_HTML" id="MO2"></graphic></fig><fig id="Fig3"><label>Fig. 3</label><caption><p>HPC, CFU-Hill and ECFC counts in peripheral venous blood of patients with pulmonary hypertension according to treatment subtype. <bold>a</bold> No difference is observed in HPC according to treatment subtype (oral <italic>mono and/or bitherapy</italic> with or without subcutaneous treprostinil with respectively, a <italic>P</italic> = 0.52 and 0.76 vs. not treated PAH). <bold>b</bold> No difference is observed in CFU-Hill colonies determined by cell culture according to treatment subtype (oral <italic>mono and/or bitherapy</italic> with or without subcutaneous treprostinil with respectively, a <italic>P</italic> = 0.64 and 0.19 vs. not treated PAH). <bold>c</bold> No difference is observed in ECFC determined by cell culture after oral <italic>mono and/or bitherapy</italic> (<italic>P</italic> = 0.22) while a significant increase in ECFC was observed with subcutaneous treprostinil treatment (* <italic>P</italic> = 0.04)</p></caption><graphic xlink:href="10456_2010_9192_Fig3_HTML" id="MO3"></graphic></fig></p></sec><sec id="Sec14"><title>Treprostinil enhances the proangiogenic potential of ECFC</title><p>ECFC from patients receiving oral therapy, with or without SC treprostinil, were grown to confluence from single colonies. They retained the characteristic cobblestone aspect through numerous passages and stained positive for typical endothelial markers CD34, CD146, CD144, PAR-1 thrombin receptor and von Willebrand factor (data not shown). During the first 30 days of culture, cells cultured from patients receiving oral therapy plus SC treprostinil showed enhanced proliferation in EBM, 5% FBS compared to cells from patients receiving only oral therapy (Fig. <xref rid="Fig4" ref-type="fig">4</xref>a). In vitro vascular network formation in Matrigel was similar with ECFC from patients treated with or without treprostinil (Fig. <xref rid="Fig4" ref-type="fig">4</xref>b, c), as was VEGF-induced migration in the wound healing assay (Fig. <xref rid="Fig4" ref-type="fig">4</xref>d, e).<fig id="Fig4"><label>Fig. 4</label><caption><p>Angiogenic potential of ECFC isolated from patients with pulmonary hypertension receiving vasodilator treatment. Each patient-derived ECFC were individually analyzed for proliferation and angiogenic properties in vitro and in vivo. At least 4 different patients derived-ECFC were used in each case. <bold>a</bold> Cells from patients receiving oral therapy and SC treprostinil showed an increased proliferative potential (in EBM, 5% FBS) compared with those from patients receiving oral therapy. Results are presented normalized to ECFC from cord blood (100%). The mean and SEM of three experiments are shown <italic>P</italic> < 0.05. <bold>b</bold>, <bold>c</bold> ECFC isolated from patients receiving oral therapy, with or without SC treprostinil, form intact vascular networks with similar efficiency. The mean and SEM of three experiments are shown. <bold>d</bold>, <bold>e</bold> VEGF-stimulated migration of ECFC in vitro in a wound healing assay was similar in patients receiving oral therapy with or without SC treprostinil. The mean and SEM of three experiments are shown. <bold>f</bold>, <bold>g</bold> ECFC from patients receiving oral therapy, with or without SC treprostinil, were injected intravenously into nude mice having undergone femoral artery ligature. Injection of ECFC from patients receiving oral therapy only improved foot perfusion on day 14 to the same extent as control ECFC isolated from cord blood. ECFC from patients receiving oral therapy plus SC treprostinil improved foot perfusion on day 14 by 25% more than ECFC from patients receiving oral therapy alone (<italic>P</italic> = 0.012) and ECFC isolated from cord blood (<italic>P</italic> = 0.019)</p></caption><graphic xlink:href="10456_2010_9192_Fig4_HTML" id="MO4"></graphic></fig></p><p>In the preclinical model of hindlimb ischemia, 1 × 10<sup>5</sup> ECFC from each treatment group were injected intravenously into nude mice with femoral artery ligature. Injection of ECFC from patients on oral therapy or from cord blood improved foot perfusion to a similar extent on day 14, while ECFC from treprostinil-treated patients improved foot perfusion on day 14 compared to ECFC from patients on oral therapy without SC treprostinil (<italic>P</italic> = 0.012) and ECFC from cord blood (<italic>P</italic> = 0.019, Fig. <xref rid="Fig4" ref-type="fig">4</xref>f, g)<italic>.</italic></p></sec></sec><sec id="Sec15"><title>Discussion</title><p>Subcutaneous treprostinil markedly enhanced the number and functional capacity of ECFC isolated from children with severe PAH. As these cells are involved in angiogenesis and endothelial repair, this finding provides important insights into the mechanism of action of prostacyclin therapy in this setting.</p><p>The endothelium plays a central role in pulmonary vascular regulation, and endothelial dysfunction is increasingly viewed as critical for disease initiation and progression [<xref ref-type="bibr" rid="CR3">3</xref>, <xref ref-type="bibr" rid="CR30">30</xref>]. We suspected that pharmacological treatment efficacy could be due, at least in part, to the endothelial repair capacity of ECFC. Irreversible and idiopathic PAH are associated with vascular remodeling and with smooth muscle and endothelial cell proliferation. Plexiform lesions have a similar histological aspect in idiopathic and irreversible PAH. We recently observed neoangiogenesis in lung surgical biopsy samples from patients with irreversible PAH due to CHD. This was associated to a proliferative endothelial phenotype with resistance to apoptosis [<xref ref-type="bibr" rid="CR4">4</xref>]. These findings are consistent with a compensatory adaptive response to increased pulmonary blood flow and arterial pressure [<xref ref-type="bibr" rid="CR31">31</xref>, <xref ref-type="bibr" rid="CR32">32</xref>], in which ECFC are likely to play an important role. Standard methods used to assess endothelial function in the pulmonary circulation are invasive and complex [<xref ref-type="bibr" rid="CR33">33</xref>], but recently developed ex vivo evaluations of endothelial biology have the potential to provide important insights [<xref ref-type="bibr" rid="CR34">34</xref>].</p><p>In the past 20 years, pulmonary “vasodilator” therapy has greatly improved the prognosis of patients with PAH [<xref ref-type="bibr" rid="CR19">19</xref>, <xref ref-type="bibr" rid="CR20">20</xref>], it is now clear that these agents do more than simply dilate pulmonary arterioles. Indeed, such treatments have been found to enhance revascularization and/or EPC recruitment in preclinical studies [<xref ref-type="bibr" rid="CR35">35</xref>–<xref ref-type="bibr" rid="CR37">37</xref>] and more recently in patients with critical limb ischemia [<xref ref-type="bibr" rid="CR38">38</xref>]. Although phosphodiesterase 5 (PDE5) inhibitors [<xref ref-type="bibr" rid="CR39">39</xref>–<xref ref-type="bibr" rid="CR41">41</xref>] and endothelin receptor antagonists (ERA) [<xref ref-type="bibr" rid="CR42">42</xref>–<xref ref-type="bibr" rid="CR44">44</xref>] improve hemodynamic parameters, they have not been shown to significantly reduce mortality of PAH patients, contrary to prostanoids.</p><p>This difference between prostanoid, PDE5 inhibitors and ERA therapy in terms of mortality could result, at least in part, from a prostanoid-induced enhancement of EPC numbers and functional capacity, leading to improved vascular repair and/or new vessel formation. Two clinical studies recently showed that transplantation of angiogenic cells improved exercise capacity and pulmonary hemodynamics in adults and children with idiopathic pulmonary hypertension [<xref ref-type="bibr" rid="CR17">17</xref>, <xref ref-type="bibr" rid="CR18">18</xref>]. In patients with critical leg ischemia, we recently showed that bone marrow mononuclear cell therapy induced the formation of new vessels containing endothelial cells with a ECFC phenotype [<xref ref-type="bibr" rid="CR6">6</xref>]. Moreover, Yoder et al. [<xref ref-type="bibr" rid="CR7">7</xref>] have shown that transplanted ECFC acquire a complete endothelial phenotype, maintain a high proliferative potential, and participate in endothelial healing and angiogenesis. In this study, we showed an increase of foot perfusion in the preclinical model of hindlimb ischemia of ECFC isolated from patients treated with treprostinil. Since human cells are hardly detectable in the muscle vasculature, we cannot exclude a paracrine effect of ECFC isolated from patients receiving treprostinil. Indeed, ECFC have been described to secrete several angiogenic pathways that modulate their ability to increase foot perfusion in this preclinical model [<xref ref-type="bibr" rid="CR27">27</xref>].</p><p>The main result of our study is that prostanoid therapy (contrary to PDE5 inhibitors and ERA therapy) increased the numbers and proliferative capacity of ECFC. ECFC have been shown to possess all the characteristics of true endothelial progenitors, based on the clonal relation between EPC and hematopoietic stem cells in patients with myeloproliferative disorders. Indeed, ECFC lack disease markers expressed by early EPC (CFU-Hill or CFU-EC), supporting the concept that CFU-Hill belong to the hematopoietic lineage. This suggests that, in patients with chronic myeloproliferative disorders, ECFC have an origin distinct from that of the hematopoietic malignant clone [<xref ref-type="bibr" rid="CR7">7</xref>, <xref ref-type="bibr" rid="CR45">45</xref>], and probably have true vasculogenic potential [<xref ref-type="bibr" rid="CR7">7</xref>]. Here we explored ECFC in prostanoid-treated and -untreated patients with PAH, a well-characterized vascular disorder, and found that only ECFC were modified by prostanoid treatment, the only therapy shown to reduce mortality among adults and children with PAH [<xref ref-type="bibr" rid="CR46">46</xref>–<xref ref-type="bibr" rid="CR49">49</xref>]. Our results confirm importance of ECFC in PAH. Indeed, Toshner et al<italic>.</italic> [<xref ref-type="bibr" rid="CR22">22</xref>] describe in patients with PAH and <italic>BMPRII</italic> mutations that ECFC had a hyperproliferative phenotype and an impaired capacity to form vascular networks, despite an absence of difference in ECFC numbers.</p><p>In the present study, CFU-Hill numbers did not differ between the three groups of patients, and did not change during treatment. Results of early-EPC or CFU-Hill counts in PAH are controversial. Asosingh et al<italic>.</italic> [<xref ref-type="bibr" rid="CR8">8</xref>] found significantly increased numbers of early EPC in PAH patients compared with controls. In contrast, Junhui et al. [<xref ref-type="bibr" rid="CR9">9</xref>] found reduced numbers of early EPC, with functional defects, in idiopathic PAH patients compared with controls, a finding confirmed by Diller et al<italic>.</italic> [<xref ref-type="bibr" rid="CR10">10</xref>].</p><p>One limitation of our study is that we did not study the functional status of ECFC from healthy children. In addition, we did not attempt to confirm our findings with another prostanoid, such as IV prostacyclin, that has also been shown to improve survival in this setting.</p><p>The higher counts and enhanced angiogenic properties of ECFC in children treated with treprostinil indicate that these cells could contribute to the compensatory adaptive response to increased pulmonary blood flow and/or pressure. It is thus tempting to speculate that ECFC expanded ex vivo might be beneficial in pediatric PAH, especially given the higher counts and functional capacities of ECFC in children compared with adults. Indeed, despite the lack of data on normal ECFC values in children, we found that the ECFC yield in culture for the two older groups of children (with idiopathic and irreversible PAH) was similar to that found in adults [0.2 and 0.6 colonies per 5 × 10<sup>6</sup> MNC, respectively, in irreversible and idiopathic PAH, vs 2.0 in reversible PAH and 0.3 in healthy adults (<italic>D. Smadja, personal data</italic>)]. These results are in line with those of Yoder’s group, who observed a hierarchy of proliferative potential between cord blood and adult blood. This result can reasonably be extrapolated to children less than 5 years old, as was the case of our patients with reversible PAH (median age 2 years).</p><p>In conclusion, this study suggests that prostanoids enhance the number and proliferative capacities of ECFC in children with pulmonary hypertension, an effect that may contribute to endothelial repair and/or new vessel formation and, thus, to the observed clinical benefits. The potential interest of ECFC count as a surrogate marker of prostanoid treatment efficacy is currently being investigated.</p></sec></body><back><ack><p>We thank Isabelle Zezepanski, Blandine Dizier, Sébastien Bertil, Florence Desvard, Yolande Daigneau, Florence Dao, Yann Burnel and Evelyne Galtier for their excellent technical assistance. This work was supported by research grants from the Leducq TransAtlantic Network of Excellence on Atherothrombosis Research (Grant 04CVD01), Leg Poix (Paris, France) and ARCFA (association pour la recherche en cardiologie du foetus à l’adulte).</p><p><bold>Conflict of interest</bold> None.</p><p><bold>Open Access</bold> This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.</p></ack><ref-list id="Bib1"><title>References</title><ref id="CR1"><label>1.</label><mixed-citation publication-type="journal"><person-group 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