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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Validation of the cantharidin-induced skin blister as an <italic>in vivo</italic>
model of inflammation</title>
<author><name sortKey="Dinh, Phong Huy Duc" sort="Dinh, Phong Huy Duc" uniqKey="Dinh P" first="Phong Huy Duc" last="Dinh">Phong Huy Duc Dinh</name>
<affiliation><nlm:aff id="au1"><institution>Clinics of Immuno-allergology</institution>
<addr-line>Brussels, Belgium</addr-line>
</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="au3"><institution>Department of Immunology, Pham Ngoc Thach University of Medicine (PNTU)</institution>
<addr-line>Ho Chi Minh City, Vietnam</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Corraza, Francis" sort="Corraza, Francis" uniqKey="Corraza F" first="Francis" last="Corraza">Francis Corraza</name>
<affiliation><nlm:aff id="au2"><institution>Hematology, CHU Brugmann (Université Libre de Bruxelles – ULB)</institution>
<addr-line>Brussels, Belgium</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Mestdagh, Kristel" sort="Mestdagh, Kristel" uniqKey="Mestdagh K" first="Kristel" last="Mestdagh">Kristel Mestdagh</name>
<affiliation><nlm:aff id="au1"><institution>Clinics of Immuno-allergology</institution>
<addr-line>Brussels, Belgium</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Kassengera, Zaina" sort="Kassengera, Zaina" uniqKey="Kassengera Z" first="Zaina" last="Kassengera">Zaina Kassengera</name>
<affiliation><nlm:aff id="au2"><institution>Hematology, CHU Brugmann (Université Libre de Bruxelles – ULB)</institution>
<addr-line>Brussels, Belgium</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Doyen, Virginie" sort="Doyen, Virginie" uniqKey="Doyen V" first="Virginie" last="Doyen">Virginie Doyen</name>
<affiliation><nlm:aff id="au1"><institution>Clinics of Immuno-allergology</institution>
<addr-line>Brussels, Belgium</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Michel, Olivier" sort="Michel, Olivier" uniqKey="Michel O" first="Olivier" last="Michel">Olivier Michel</name>
<affiliation><nlm:aff id="au1"><institution>Clinics of Immuno-allergology</institution>
<addr-line>Brussels, Belgium</addr-line>
</nlm:aff>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PMC</idno>
<idno type="pmid">21595743</idno>
<idno type="pmc">3244638</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3244638</idno>
<idno type="RBID">PMC:3244638</idno>
<idno type="doi">10.1111/j.1365-2125.2011.04020.x</idno>
<date when="2011">2011</date>
<idno type="wicri:Area/Pmc/Corpus">002C89</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">002C89</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Validation of the cantharidin-induced skin blister as an <italic>in vivo</italic>
model of inflammation</title>
<author><name sortKey="Dinh, Phong Huy Duc" sort="Dinh, Phong Huy Duc" uniqKey="Dinh P" first="Phong Huy Duc" last="Dinh">Phong Huy Duc Dinh</name>
<affiliation><nlm:aff id="au1"><institution>Clinics of Immuno-allergology</institution>
<addr-line>Brussels, Belgium</addr-line>
</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="au3"><institution>Department of Immunology, Pham Ngoc Thach University of Medicine (PNTU)</institution>
<addr-line>Ho Chi Minh City, Vietnam</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Corraza, Francis" sort="Corraza, Francis" uniqKey="Corraza F" first="Francis" last="Corraza">Francis Corraza</name>
<affiliation><nlm:aff id="au2"><institution>Hematology, CHU Brugmann (Université Libre de Bruxelles – ULB)</institution>
<addr-line>Brussels, Belgium</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Mestdagh, Kristel" sort="Mestdagh, Kristel" uniqKey="Mestdagh K" first="Kristel" last="Mestdagh">Kristel Mestdagh</name>
<affiliation><nlm:aff id="au1"><institution>Clinics of Immuno-allergology</institution>
<addr-line>Brussels, Belgium</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Kassengera, Zaina" sort="Kassengera, Zaina" uniqKey="Kassengera Z" first="Zaina" last="Kassengera">Zaina Kassengera</name>
<affiliation><nlm:aff id="au2"><institution>Hematology, CHU Brugmann (Université Libre de Bruxelles – ULB)</institution>
<addr-line>Brussels, Belgium</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Doyen, Virginie" sort="Doyen, Virginie" uniqKey="Doyen V" first="Virginie" last="Doyen">Virginie Doyen</name>
<affiliation><nlm:aff id="au1"><institution>Clinics of Immuno-allergology</institution>
<addr-line>Brussels, Belgium</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Michel, Olivier" sort="Michel, Olivier" uniqKey="Michel O" first="Olivier" last="Michel">Olivier Michel</name>
<affiliation><nlm:aff id="au1"><institution>Clinics of Immuno-allergology</institution>
<addr-line>Brussels, Belgium</addr-line>
</nlm:aff>
</affiliation>
</author>
</analytic>
<series><title level="j">British Journal of Clinical Pharmacology</title>
<idno type="ISSN">0306-5251</idno>
<idno type="eISSN">1365-2125</idno>
<imprint><date when="2011">2011</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass></textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en"><sec><title>AIM</title>
<p>Pharmacological profiling techniques, such as the cantharidin-induced skin blister, may be used to assess the anti-inflammatory properties of novel drugs. However, no data are available on the reproducibility of this technique or on the blocking effect of anti-inflammatory drugs, such as anti-TNF and corticosteroids.</p>
</sec>
<sec><title>METHODS</title>
<p>A group of 30 healthy subjects were randomized into three parallel groups treated with placebo, oral methylprednisolone 20 mg day<sup>−1</sup>
for 7 days or anti-tumour necrosis factor (TNF) (adalimumab, Humira®, Abbott) 40 mg s.c. single dose. A first blister was induced at baseline and collected, immediately before the start of treatment and a second blister was obtained 7 days after the start of treatment. The total number of cells, the cell viability and the differential cell count were evaluated by two independent observers, who were blind to treatment. <sc>anova</sc>
was used to compare change from baseline among the three groups before pairwise comparisons.</p>
</sec>
<sec><title>RESULTS</title>
<p>Among the placebo group, there was no significant difference in the total cell count, neutrophils, eosinophils and monocytes between day 1 and day 7. Methylprednisolone inhibited the eosinophil influx in mean % (95% CI) (−1.0 (−1.7, −0.3); <italic>P</italic>
< 0.02) and absolute (<italic>P</italic>
< 0.02) values, while anti-TNF inhibited the neutrophil influx in mean % (95% CI) (−19.3 (−29.5, −9.1); <italic>P</italic>
< 0.01) and absolute (<italic>P</italic>
< 0.05) values.</p>
</sec>
<sec><title>CONCLUSIONS</title>
<p>The cantharidin-induced skin blister is a safe, well tolerated and reproducible procedure. Pre-treatment with anti-TNF or methylprednisolone inhibited the neutrophilic or eosinophilic trafficking, respectively. It could be useful in profiling anti-inflammatory drugs regarding their effects on the cellular inflammatory response.</p>
</sec>
</div>
</front>
</TEI>
<pmc article-type="research-article"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Br J Clin Pharmacol</journal-id>
<journal-id journal-id-type="publisher-id">bcp</journal-id>
<journal-title-group><journal-title>British Journal of Clinical Pharmacology</journal-title>
</journal-title-group>
<issn pub-type="ppub">0306-5251</issn>
<issn pub-type="epub">1365-2125</issn>
<publisher><publisher-name>Blackwell Science Inc</publisher-name>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">21595743</article-id>
<article-id pub-id-type="pmc">3244638</article-id>
<article-id pub-id-type="doi">10.1111/j.1365-2125.2011.04020.x</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Clinical Trials</subject>
</subj-group>
</article-categories>
<title-group><article-title>Validation of the cantharidin-induced skin blister as an <italic>in vivo</italic>
model of inflammation</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Dinh</surname>
<given-names>Phong Huy Duc</given-names>
</name>
<xref ref-type="aff" rid="au1">1</xref>
<xref ref-type="aff" rid="au3">3</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Corraza</surname>
<given-names>Francis</given-names>
</name>
<xref ref-type="aff" rid="au2">2</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Mestdagh</surname>
<given-names>Kristel</given-names>
</name>
<xref ref-type="aff" rid="au1">1</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Kassengera</surname>
<given-names>Zaina</given-names>
</name>
<xref ref-type="aff" rid="au2">2</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Doyen</surname>
<given-names>Virginie</given-names>
</name>
<xref ref-type="aff" rid="au1">1</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Michel</surname>
<given-names>Olivier</given-names>
</name>
<xref ref-type="aff" rid="au1">1</xref>
</contrib>
<aff id="au1"><label>1</label>
<institution>Clinics of Immuno-allergology</institution>
<addr-line>Brussels, Belgium</addr-line>
</aff>
<aff id="au2"><label>2</label>
<institution>Hematology, CHU Brugmann (Université Libre de Bruxelles – ULB)</institution>
<addr-line>Brussels, Belgium</addr-line>
</aff>
<aff id="au3"><label>3</label>
<institution>Department of Immunology, Pham Ngoc Thach University of Medicine (PNTU)</institution>
<addr-line>Ho Chi Minh City, Vietnam</addr-line>
</aff>
</contrib-group>
<author-notes><corresp id="cor1">Dr Olivier Michel MD PhD, CHU Brugmann/ULB – Université Libre de Bruxelles, place Van Gehuchten, 4, B −1020 Brussels, Belgium. Tel.: +32 2 477 2272, Fax: +32 2 477 2276, E-mail: <email>omichel@ulb.ac.be</email>
</corresp>
</author-notes>
<pub-date pub-type="ppub"><month>12</month>
<year>2011</year>
</pub-date>
<volume>72</volume>
<issue>6</issue>
<fpage>912</fpage>
<lpage>920</lpage>
<history><date date-type="received"><day>22</day>
<month>11</month>
<year>2010</year>
</date>
<date date-type="accepted"><day>13</day>
<month>5</month>
<year>2011</year>
</date>
<date date-type="accepted"><day>19</day>
<month>5</month>
<year>2011</year>
</date>
</history>
<permissions><copyright-statement>Copyright © 2011 The British Pharmacological Society</copyright-statement>
<copyright-year>2011</copyright-year>
</permissions>
<abstract><sec><title>AIM</title>
<p>Pharmacological profiling techniques, such as the cantharidin-induced skin blister, may be used to assess the anti-inflammatory properties of novel drugs. However, no data are available on the reproducibility of this technique or on the blocking effect of anti-inflammatory drugs, such as anti-TNF and corticosteroids.</p>
</sec>
<sec><title>METHODS</title>
<p>A group of 30 healthy subjects were randomized into three parallel groups treated with placebo, oral methylprednisolone 20 mg day<sup>−1</sup>
for 7 days or anti-tumour necrosis factor (TNF) (adalimumab, Humira®, Abbott) 40 mg s.c. single dose. A first blister was induced at baseline and collected, immediately before the start of treatment and a second blister was obtained 7 days after the start of treatment. The total number of cells, the cell viability and the differential cell count were evaluated by two independent observers, who were blind to treatment. <sc>anova</sc>
was used to compare change from baseline among the three groups before pairwise comparisons.</p>
</sec>
<sec><title>RESULTS</title>
<p>Among the placebo group, there was no significant difference in the total cell count, neutrophils, eosinophils and monocytes between day 1 and day 7. Methylprednisolone inhibited the eosinophil influx in mean % (95% CI) (−1.0 (−1.7, −0.3); <italic>P</italic>
< 0.02) and absolute (<italic>P</italic>
< 0.02) values, while anti-TNF inhibited the neutrophil influx in mean % (95% CI) (−19.3 (−29.5, −9.1); <italic>P</italic>
< 0.01) and absolute (<italic>P</italic>
< 0.05) values.</p>
</sec>
<sec><title>CONCLUSIONS</title>
<p>The cantharidin-induced skin blister is a safe, well tolerated and reproducible procedure. Pre-treatment with anti-TNF or methylprednisolone inhibited the neutrophilic or eosinophilic trafficking, respectively. It could be useful in profiling anti-inflammatory drugs regarding their effects on the cellular inflammatory response.</p>
</sec>
</abstract>
<kwd-group><kwd>anti-TNF</kwd>
<kwd>blister</kwd>
<kwd>cantharidin</kwd>
<kwd>inflammation</kwd>
<kwd>steroids</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
</record>
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