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Der p 11 Is a Major Allergen for House Dust Mite-Allergic Patients Suffering from Atopic Dermatitis

Identifieur interne : 001D58 ( Pmc/Corpus ); précédent : 001D57; suivant : 001D59

Der p 11 Is a Major Allergen for House Dust Mite-Allergic Patients Suffering from Atopic Dermatitis

Auteurs : Srinita Banerjee ; Yvonne Resch ; Kuan-Wei Chen ; Ines Swoboda ; Margit Focke-Tejkl ; Katharina Blatt ; Natalija Novak ; Magnus Wickman ; Marianne Van Hage ; Rosetta Ferrara ; Adriano Mari ; Ashok Purohit ; Gabrielle Pauli ; Elopy N. Sibanda ; Portia Ndlovu ; Wayne R. Thomas ; Vladislav Krzyzanek ; Sebastian Tacke ; Ursula Malkus ; Peter Valent ; Rudolf Valenta ; Susanne Vrtala

Source :

RBID : PMC:4636057

Abstract

House dust mites (HDMs) belong to the most potent indoor allergen sources worldwide and are associated with allergic manifestations in the respiratory tract and the skin. Here we studied the importance of the high-molecular-weight group 11 allergen from Dermatophagoides pteronyssinus (Der p 11) in HDM allergy. Sequence analysis showed that Der p 11 has high homology to paramyosins from mites, ticks, and other invertebrates. A synthetic gene coding for Der p 11 was expressed in Escherichia coli and rDer p 11 purified to homogeneity as folded, alpha-helical protein as determined by circular dichroism spectroscopy. Using antibodies raised against rDer p 11 and immunogold electron microscopy, the allergen was localized in the muscle beneath the skin of mite bodies but not in feces. IgE reactivity of rDer p 11 was tested with sera from HDM-allergic patients from Europe and Africa in radioallergosorbent test–based dot-blot assays. Interestingly, we found that Der p 11 is a major allergen for patients suffering from atopic dermatitis (AD), whereas it is only a minor allergen for patients suffering from respiratory forms of HDM allergy. Thus, rDer p 11 might be a useful serological marker allergen for the identification of a subgroup of HDM-allergic patients suffering from HDM-associated AD.


Url:
DOI: 10.1038/jid.2014.271
PubMed: 24999597
PubMed Central: 4636057

Links to Exploration step

PMC:4636057

Le document en format XML

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<name sortKey="Novak, Natalija" sort="Novak, Natalija" uniqKey="Novak N" first="Natalija" last="Novak">Natalija Novak</name>
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<nlm:aff id="A4">Department of Dermatology and Allergy, University of Bonn, Bonn, Germany</nlm:aff>
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<name sortKey="Wickman, Magnus" sort="Wickman, Magnus" uniqKey="Wickman M" first="Magnus" last="Wickman">Magnus Wickman</name>
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<name sortKey="Mari, Adriano" sort="Mari, Adriano" uniqKey="Mari A" first="Adriano" last="Mari">Adriano Mari</name>
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<nlm:aff id="A8">Service de Pneumologie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France</nlm:aff>
</affiliation>
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<name sortKey="Sibanda, Elopy N" sort="Sibanda, Elopy N" uniqKey="Sibanda E" first="Elopy N." last="Sibanda">Elopy N. Sibanda</name>
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<nlm:aff id="A9">Gamma City Laboratory, Harare, Zimbabwe</nlm:aff>
</affiliation>
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<name sortKey="Ndlovu, Portia" sort="Ndlovu, Portia" uniqKey="Ndlovu P" first="Portia" last="Ndlovu">Portia Ndlovu</name>
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<nlm:aff id="A9">Gamma City Laboratory, Harare, Zimbabwe</nlm:aff>
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</affiliation>
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<name sortKey="Krzyzanek, Vladislav" sort="Krzyzanek, Vladislav" uniqKey="Krzyzanek V" first="Vladislav" last="Krzyzanek">Vladislav Krzyzanek</name>
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<nlm:aff id="A3">Division of Hematology and Hemostaseology, Department of Internal Medicine I, Medical University of Vienna, Vienna, Austria</nlm:aff>
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<name sortKey="Valenta, Rudolf" sort="Valenta, Rudolf" uniqKey="Valenta R" first="Rudolf" last="Valenta">Rudolf Valenta</name>
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<nlm:aff id="A1">Division of Immunopathology, Department of Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria</nlm:aff>
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<nlm:aff id="A2">Christian Doppler Laboratory for Allergy Research, Medical University of Vienna, Vienna, Austria</nlm:aff>
</affiliation>
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<nlm:aff id="A13">Christian Doppler Laboratory for the Development of Allergen Chips, Department of Pathophysiology and Allergy Research, Medical University of Vienna, Vienna, Austria</nlm:aff>
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<p id="P3">House dust mites (HDMs) belong to the most potent indoor allergen sources worldwide and are associated with allergic manifestations in the respiratory tract and the skin. Here we studied the importance of the high-molecular-weight group 11 allergen from
<italic>Dermatophagoides pteronyssinus</italic>
(Der p 11) in HDM allergy. Sequence analysis showed that Der p 11 has high homology to paramyosins from mites, ticks, and other invertebrates. A synthetic gene coding for Der p 11 was expressed in
<italic>Escherichia coli</italic>
and rDer p 11 purified to homogeneity as folded, alpha-helical protein as determined by circular dichroism spectroscopy. Using antibodies raised against rDer p 11 and immunogold electron microscopy, the allergen was localized in the muscle beneath the skin of mite bodies but not in feces. IgE reactivity of rDer p 11 was tested with sera from HDM-allergic patients from Europe and Africa in radioallergosorbent test–based dot-blot assays. Interestingly, we found that Der p 11 is a major allergen for patients suffering from atopic dermatitis (AD), whereas it is only a minor allergen for patients suffering from respiratory forms of HDM allergy. Thus, rDer p 11 might be a useful serological marker allergen for the identification of a subgroup of HDM-allergic patients suffering from HDM-associated AD.</p>
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<name>
<surname>Swoboda</surname>
<given-names>Ines</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
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<surname>Wickman</surname>
<given-names>Magnus</given-names>
</name>
<xref ref-type="aff" rid="A5">5</xref>
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<contrib contrib-type="author">
<name>
<surname>van Hage</surname>
<given-names>Marianne</given-names>
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<contrib contrib-type="author">
<name>
<surname>Mari</surname>
<given-names>Adriano</given-names>
</name>
<xref ref-type="aff" rid="A7">7</xref>
<xref ref-type="author-notes" rid="FN2">15</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Purohit</surname>
<given-names>Ashok</given-names>
</name>
<xref ref-type="aff" rid="A8">8</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Pauli</surname>
<given-names>Gabrielle</given-names>
</name>
<xref ref-type="aff" rid="A8">8</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Sibanda</surname>
<given-names>Elopy N.</given-names>
</name>
<xref ref-type="aff" rid="A9">9</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ndlovu</surname>
<given-names>Portia</given-names>
</name>
<xref ref-type="aff" rid="A9">9</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Thomas</surname>
<given-names>Wayne R.</given-names>
</name>
<xref ref-type="aff" rid="A10">10</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Krzyzanek</surname>
<given-names>Vladislav</given-names>
</name>
<xref ref-type="aff" rid="A11">11</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Tacke</surname>
<given-names>Sebastian</given-names>
</name>
<xref ref-type="aff" rid="A12">12</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Malkus</surname>
<given-names>Ursula</given-names>
</name>
<xref ref-type="aff" rid="A12">12</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Valent</surname>
<given-names>Peter</given-names>
</name>
<xref ref-type="aff" rid="A3">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Valenta</surname>
<given-names>Rudolf</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
<xref ref-type="aff" rid="A2">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Vrtala</surname>
<given-names>Susanne</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
<xref ref-type="aff" rid="A13">13</xref>
</contrib>
</contrib-group>
<aff id="A1">
<label>1</label>
Division of Immunopathology, Department of Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria</aff>
<aff id="A2">
<label>2</label>
Christian Doppler Laboratory for Allergy Research, Medical University of Vienna, Vienna, Austria</aff>
<aff id="A3">
<label>3</label>
Division of Hematology and Hemostaseology, Department of Internal Medicine I, Medical University of Vienna, Vienna, Austria</aff>
<aff id="A4">
<label>4</label>
Department of Dermatology and Allergy, University of Bonn, Bonn, Germany</aff>
<aff id="A5">
<label>5</label>
Sachs’ Children’s Hospital and Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden</aff>
<aff id="A6">
<label>6</label>
Clinical Immunology and Allergy Unit, Department of Medicine Solna, Karolinska Institutet and University Hospital Stockholm, Stockholm, Sweden</aff>
<aff id="A7">
<label>7</label>
Center for Molecular Allergology, IDI-IRCCS, Rome, Italy</aff>
<aff id="A8">
<label>8</label>
Service de Pneumologie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France</aff>
<aff id="A9">
<label>9</label>
Gamma City Laboratory, Harare, Zimbabwe</aff>
<aff id="A10">
<label>10</label>
Center for Child Health Research, Telethon Institute of Child Health Research, University of Western Australia, Perth, Australia</aff>
<aff id="A11">
<label>11</label>
Institute of Scientific Instruments, Academy of Sciences of the Czech Republic, Brno, Czech Republic</aff>
<aff id="A12">
<label>12</label>
Institute of Medical Physics and Biophysics, University of Münster, Münster, Germany</aff>
<aff id="A13">
<label>13</label>
Christian Doppler Laboratory for the Development of Allergen Chips, Department of Pathophysiology and Allergy Research, Medical University of Vienna, Vienna, Austria</aff>
<author-notes>
<corresp id="CR1">Correspondence: Susanne Vrtala, Christian Doppler Laboratory for the Development of Allergen Chips, Department of Pathophysiology and Allergy Research, Medical University of Vienna, Waehringer Guertel 18-20, 1090 Vienna, Austria.
<email>susanne.vrtala@meduniwien.ac.at</email>
</corresp>
<fn fn-type="present-address" id="FN1">
<label>14</label>
<p id="P1">Present address: Section of Molecular Biotechnology, University of Applied Science, Campus Vienna Biocenter, Vienna, Austria.</p>
</fn>
<fn fn-type="present-address" id="FN2">
<label>15</label>
<p id="P2">Present address: Associated Centers for Molecular Allergology, Rome, Italy.</p>
</fn>
</author-notes>
<pub-date pub-type="nihms-submitted">
<day>2</day>
<month>11</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="epub">
<day>07</day>
<month>8</month>
<year>2014</year>
</pub-date>
<pub-date pub-type="ppub">
<month>1</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="pmc-release">
<day>06</day>
<month>11</month>
<year>2015</year>
</pub-date>
<volume>135</volume>
<issue>1</issue>
<fpage>102</fpage>
<lpage>109</lpage>
<pmc-comment>elocation-id from pubmed: 10.1038/jid.2014.271</pmc-comment>
<abstract>
<p id="P3">House dust mites (HDMs) belong to the most potent indoor allergen sources worldwide and are associated with allergic manifestations in the respiratory tract and the skin. Here we studied the importance of the high-molecular-weight group 11 allergen from
<italic>Dermatophagoides pteronyssinus</italic>
(Der p 11) in HDM allergy. Sequence analysis showed that Der p 11 has high homology to paramyosins from mites, ticks, and other invertebrates. A synthetic gene coding for Der p 11 was expressed in
<italic>Escherichia coli</italic>
and rDer p 11 purified to homogeneity as folded, alpha-helical protein as determined by circular dichroism spectroscopy. Using antibodies raised against rDer p 11 and immunogold electron microscopy, the allergen was localized in the muscle beneath the skin of mite bodies but not in feces. IgE reactivity of rDer p 11 was tested with sera from HDM-allergic patients from Europe and Africa in radioallergosorbent test–based dot-blot assays. Interestingly, we found that Der p 11 is a major allergen for patients suffering from atopic dermatitis (AD), whereas it is only a minor allergen for patients suffering from respiratory forms of HDM allergy. Thus, rDer p 11 might be a useful serological marker allergen for the identification of a subgroup of HDM-allergic patients suffering from HDM-associated AD.</p>
</abstract>
</article-meta>
</front>
</pmc>
</record>

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