An official European Respiratory Society/American Thoracic Society research statement: interstitial pneumonia with autoimmune features.
Identifieur interne : 002784 ( PubMed/Curation ); précédent : 002783; suivant : 002785An official European Respiratory Society/American Thoracic Society research statement: interstitial pneumonia with autoimmune features.
Auteurs : Aryeh Fischer [États-Unis] ; Katerina M. Antoniou [Grèce] ; Kevin K. Brown [États-Unis] ; Jacques Cadranel [France] ; Tamera J. Corte ; Roland M. Du Bois [Royaume-Uni] ; Joyce S. Lee ; Kevin O. Leslie [États-Unis] ; David A. Lynch [États-Unis] ; Eric L. Matteson [États-Unis] ; Marta Mosca [Italie] ; Imre Noth [États-Unis] ; Luca Richeldi [Royaume-Uni] ; Mary E. Strek ; Jeffrey J. Swigris ; Athol U. Wells [Royaume-Uni] ; Sterling G. West [États-Unis] ; Harold R. Collard ; Vincent CottinSource :
- The European respiratory journal [ 1399-3003 ] ; 2015.
Descripteurs français
- KwdFr :
- Auto-immunité, Autoanticorps (), Europe, Humains, Maladies auto-immunes (), Maladies auto-immunes (diagnostic), Maladies du tissu conjonctif (immunologie), Pneumologie (normes), Pneumopathies interstitielles (), Pneumopathies interstitielles (diagnostic), Pneumopathies interstitielles (immunologie), Pneumopathies interstitielles idiopathiques (), Pneumopathies interstitielles idiopathiques (diagnostic), Pneumopathies interstitielles idiopathiques (immunologie), Sociétés médicales, États-Unis d'Amérique, Études prospectives.
- MESH :
- diagnostic : Maladies auto-immunes, Pneumopathies interstitielles, Pneumopathies interstitielles idiopathiques.
- immunologie : Maladies du tissu conjonctif, Pneumopathies interstitielles, Pneumopathies interstitielles idiopathiques.
- normes : Pneumologie.
- Auto-immunité, Autoanticorps, Europe, Humains, Maladies auto-immunes, Pneumopathies interstitielles, Pneumopathies interstitielles idiopathiques, Sociétés médicales, États-Unis d'Amérique, Études prospectives.
- Wicri :
- geographic : États-Unis.
English descriptors
- KwdEn :
- Autoantibodies (chemistry), Autoimmune Diseases (diagnosis), Autoimmune Diseases (therapy), Autoimmunity, Connective Tissue Diseases (immunology), Europe, Humans, Idiopathic Interstitial Pneumonias (diagnosis), Idiopathic Interstitial Pneumonias (immunology), Idiopathic Interstitial Pneumonias (therapy), Lung Diseases, Interstitial (diagnosis), Lung Diseases, Interstitial (immunology), Lung Diseases, Interstitial (therapy), Prospective Studies, Pulmonary Medicine (standards), Societies, Medical, United States.
- MESH :
- chemical , chemistry : Autoantibodies.
- geographic : Europe, United States.
- diagnosis : Autoimmune Diseases, Idiopathic Interstitial Pneumonias, Lung Diseases, Interstitial.
- immunology : Connective Tissue Diseases, Idiopathic Interstitial Pneumonias, Lung Diseases, Interstitial.
- standards : Pulmonary Medicine.
- therapy : Autoimmune Diseases, Idiopathic Interstitial Pneumonias, Lung Diseases, Interstitial.
- Autoimmunity, Humans, Prospective Studies, Societies, Medical.
Abstract
Many patients with an idiopathic interstitial pneumonia (IIP) have clinical features that suggest an underlying autoimmune process but do not meet established criteria for a connective tissue disease (CTD). Researchers have proposed differing criteria and terms to describe these patients, and lack of consensus over nomenclature and classification limits the ability to conduct prospective studies of a uniform cohort.The "European Respiratory Society/American Thoracic Society Task Force on Undifferentiated Forms of Connective Tissue Disease-associated Interstitial Lung Disease" was formed to create consensus regarding the nomenclature and classification criteria for patients with IIP and features of autoimmunity.The task force proposes the term "interstitial pneumonia with autoimmune features" (IPAF) and offers classification criteria organised around the presence of a combination of features from three domains: a clinical domain consisting of specific extra-thoracic features, a serologic domain consisting of specific autoantibodies, and a morphologic domain consisting of specific chest imaging, histopathologic or pulmonary physiologic features.A designation of IPAF should be used to identify individuals with IIP and features suggestive of, but not definitive for, a CTD. With IPAF, a sound platform has been provided from which to launch the requisite future research investigations of a more uniform cohort.
DOI: 10.1183/13993003.00150-2015
PubMed: 26160873
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Tamera J. Corte<affiliation><nlm:affiliation>The Aldred Hospital, Melbourne, Australia Members of the writing group of the task force.</nlm:affiliation>
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<affiliation><nlm:affiliation>Medicine, University of California San Francisco, San Francisco, CA, USA Members of the writing group of the task force.</nlm:affiliation>
<wicri:noCountry code="subField">USA Members of the writing group of the task force</wicri:noCountry>
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<affiliation><nlm:affiliation>Medicine, University of Chicago, Chicago, IL, USA Members of the writing group of the task force.</nlm:affiliation>
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<affiliation><nlm:affiliation>Dept of Medicine, National Jewish Health, Denver, CO, USA Members of the writing group of the task force.</nlm:affiliation>
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<affiliation><nlm:affiliation>Medicine, University of California San Francisco, San Francisco, CA, USA Members of the writing group of the task force Task force vice-chairs, and contributed equally to this manuscript.</nlm:affiliation>
<wicri:noCountry code="subField">and contributed equally to this manuscript</wicri:noCountry>
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<affiliation><nlm:affiliation>Service de Pneumologie, Hopital L. Pradel, Lyon, France Members of the writing group of the task force Task force vice-chairs, and contributed equally to this manuscript.</nlm:affiliation>
<wicri:noCountry code="subField">and contributed equally to this manuscript</wicri:noCountry>
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Le document en format XML
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<author><name sortKey="Cottin, Vincent" sort="Cottin, Vincent" uniqKey="Cottin V" first="Vincent" last="Cottin">Vincent Cottin</name>
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<author><name sortKey="Leslie, Kevin O" sort="Leslie, Kevin O" uniqKey="Leslie K" first="Kevin O" last="Leslie">Kevin O. Leslie</name>
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<author><name sortKey="Lynch, David A" sort="Lynch, David A" uniqKey="Lynch D" first="David A" last="Lynch">David A. Lynch</name>
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<author><name sortKey="Matteson, Eric L" sort="Matteson, Eric L" uniqKey="Matteson E" first="Eric L" last="Matteson">Eric L. Matteson</name>
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<country xml:lang="fr">États-Unis</country>
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<author><name sortKey="Mosca, Marta" sort="Mosca, Marta" uniqKey="Mosca M" first="Marta" last="Mosca">Marta Mosca</name>
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<author><name sortKey="Noth, Imre" sort="Noth, Imre" uniqKey="Noth I" first="Imre" last="Noth">Imre Noth</name>
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<author><name sortKey="Richeldi, Luca" sort="Richeldi, Luca" uniqKey="Richeldi L" first="Luca" last="Richeldi">Luca Richeldi</name>
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<author><name sortKey="Strek, Mary E" sort="Strek, Mary E" uniqKey="Strek M" first="Mary E" last="Strek">Mary E. Strek</name>
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<wicri:noCountry code="subField">USA Members of the writing group of the task force</wicri:noCountry>
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<author><name sortKey="Swigris, Jeffrey J" sort="Swigris, Jeffrey J" uniqKey="Swigris J" first="Jeffrey J" last="Swigris">Jeffrey J. Swigris</name>
<affiliation><nlm:affiliation>Dept of Medicine, National Jewish Health, Denver, CO, USA Members of the writing group of the task force.</nlm:affiliation>
<wicri:noCountry code="subField">USA Members of the writing group of the task force</wicri:noCountry>
</affiliation>
</author>
<author><name sortKey="Wells, Athol U" sort="Wells, Athol U" uniqKey="Wells A" first="Athol U" last="Wells">Athol U. Wells</name>
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<author><name sortKey="West, Sterling G" sort="West, Sterling G" uniqKey="West S" first="Sterling G" last="West">Sterling G. West</name>
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<author><name sortKey="Collard, Harold R" sort="Collard, Harold R" uniqKey="Collard H" first="Harold R" last="Collard">Harold R. Collard</name>
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<wicri:noCountry code="subField">and contributed equally to this manuscript</wicri:noCountry>
</affiliation>
</author>
<author><name sortKey="Cottin, Vincent" sort="Cottin, Vincent" uniqKey="Cottin V" first="Vincent" last="Cottin">Vincent Cottin</name>
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<wicri:noCountry code="subField">and contributed equally to this manuscript</wicri:noCountry>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Autoantibodies (chemistry)</term>
<term>Autoimmune Diseases (diagnosis)</term>
<term>Autoimmune Diseases (therapy)</term>
<term>Autoimmunity</term>
<term>Connective Tissue Diseases (immunology)</term>
<term>Europe</term>
<term>Humans</term>
<term>Idiopathic Interstitial Pneumonias (diagnosis)</term>
<term>Idiopathic Interstitial Pneumonias (immunology)</term>
<term>Idiopathic Interstitial Pneumonias (therapy)</term>
<term>Lung Diseases, Interstitial (diagnosis)</term>
<term>Lung Diseases, Interstitial (immunology)</term>
<term>Lung Diseases, Interstitial (therapy)</term>
<term>Prospective Studies</term>
<term>Pulmonary Medicine (standards)</term>
<term>Societies, Medical</term>
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<term>Humains</term>
<term>Maladies auto-immunes ()</term>
<term>Maladies auto-immunes (diagnostic)</term>
<term>Maladies du tissu conjonctif (immunologie)</term>
<term>Pneumologie (normes)</term>
<term>Pneumopathies interstitielles ()</term>
<term>Pneumopathies interstitielles (diagnostic)</term>
<term>Pneumopathies interstitielles (immunologie)</term>
<term>Pneumopathies interstitielles idiopathiques ()</term>
<term>Pneumopathies interstitielles idiopathiques (diagnostic)</term>
<term>Pneumopathies interstitielles idiopathiques (immunologie)</term>
<term>Sociétés médicales</term>
<term>États-Unis d'Amérique</term>
<term>Études prospectives</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Autoantibodies</term>
</keywords>
<keywords scheme="MESH" type="geographic" xml:lang="en"><term>Europe</term>
<term>United States</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Autoimmune Diseases</term>
<term>Idiopathic Interstitial Pneumonias</term>
<term>Lung Diseases, Interstitial</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Maladies auto-immunes</term>
<term>Pneumopathies interstitielles</term>
<term>Pneumopathies interstitielles idiopathiques</term>
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<keywords scheme="MESH" qualifier="immunologie" xml:lang="fr"><term>Maladies du tissu conjonctif</term>
<term>Pneumopathies interstitielles</term>
<term>Pneumopathies interstitielles idiopathiques</term>
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<keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>Connective Tissue Diseases</term>
<term>Idiopathic Interstitial Pneumonias</term>
<term>Lung Diseases, Interstitial</term>
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<keywords scheme="MESH" qualifier="normes" xml:lang="fr"><term>Pneumologie</term>
</keywords>
<keywords scheme="MESH" qualifier="standards" xml:lang="en"><term>Pulmonary Medicine</term>
</keywords>
<keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Autoimmune Diseases</term>
<term>Idiopathic Interstitial Pneumonias</term>
<term>Lung Diseases, Interstitial</term>
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<keywords scheme="MESH" xml:lang="en"><term>Autoimmunity</term>
<term>Humans</term>
<term>Prospective Studies</term>
<term>Societies, Medical</term>
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<term>Europe</term>
<term>Humains</term>
<term>Maladies auto-immunes</term>
<term>Pneumopathies interstitielles</term>
<term>Pneumopathies interstitielles idiopathiques</term>
<term>Sociétés médicales</term>
<term>États-Unis d'Amérique</term>
<term>Études prospectives</term>
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<front><div type="abstract" xml:lang="en">Many patients with an idiopathic interstitial pneumonia (IIP) have clinical features that suggest an underlying autoimmune process but do not meet established criteria for a connective tissue disease (CTD). Researchers have proposed differing criteria and terms to describe these patients, and lack of consensus over nomenclature and classification limits the ability to conduct prospective studies of a uniform cohort.The "European Respiratory Society/American Thoracic Society Task Force on Undifferentiated Forms of Connective Tissue Disease-associated Interstitial Lung Disease" was formed to create consensus regarding the nomenclature and classification criteria for patients with IIP and features of autoimmunity.The task force proposes the term "interstitial pneumonia with autoimmune features" (IPAF) and offers classification criteria organised around the presence of a combination of features from three domains: a clinical domain consisting of specific extra-thoracic features, a serologic domain consisting of specific autoantibodies, and a morphologic domain consisting of specific chest imaging, histopathologic or pulmonary physiologic features.A designation of IPAF should be used to identify individuals with IIP and features suggestive of, but not definitive for, a CTD. With IPAF, a sound platform has been provided from which to launch the requisite future research investigations of a more uniform cohort.</div>
</front>
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<DateCreated><Year>2015</Year>
<Month>10</Month>
<Day>01</Day>
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<DateCompleted><Year>2016</Year>
<Month>08</Month>
<Day>19</Day>
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<DateRevised><Year>2015</Year>
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<Day>01</Day>
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<JournalIssue CitedMedium="Internet"><Volume>46</Volume>
<Issue>4</Issue>
<PubDate><Year>2015</Year>
<Month>Oct</Month>
</PubDate>
</JournalIssue>
<Title>The European respiratory journal</Title>
<ISOAbbreviation>Eur. Respir. J.</ISOAbbreviation>
</Journal>
<ArticleTitle>An official European Respiratory Society/American Thoracic Society research statement: interstitial pneumonia with autoimmune features.</ArticleTitle>
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<Abstract><AbstractText>Many patients with an idiopathic interstitial pneumonia (IIP) have clinical features that suggest an underlying autoimmune process but do not meet established criteria for a connective tissue disease (CTD). Researchers have proposed differing criteria and terms to describe these patients, and lack of consensus over nomenclature and classification limits the ability to conduct prospective studies of a uniform cohort.The "European Respiratory Society/American Thoracic Society Task Force on Undifferentiated Forms of Connective Tissue Disease-associated Interstitial Lung Disease" was formed to create consensus regarding the nomenclature and classification criteria for patients with IIP and features of autoimmunity.The task force proposes the term "interstitial pneumonia with autoimmune features" (IPAF) and offers classification criteria organised around the presence of a combination of features from three domains: a clinical domain consisting of specific extra-thoracic features, a serologic domain consisting of specific autoantibodies, and a morphologic domain consisting of specific chest imaging, histopathologic or pulmonary physiologic features.A designation of IPAF should be used to identify individuals with IIP and features suggestive of, but not definitive for, a CTD. With IPAF, a sound platform has been provided from which to launch the requisite future research investigations of a more uniform cohort.</AbstractText>
<CopyrightInformation>Copyright ©ERS 2015.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Fischer</LastName>
<ForeName>Aryeh</ForeName>
<Initials>A</Initials>
<AffiliationInfo><Affiliation>Dept of Medicine, University of Colorado School of Medicine, Denver, CO, USA Task force chair Members of the writing group of the task force aryeh.fischer@ucdenver.edu.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Antoniou</LastName>
<ForeName>Katerina M</ForeName>
<Initials>KM</Initials>
<AffiliationInfo><Affiliation>Thoracic Medicine, University of Crete, Heraklion, Greece.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Brown</LastName>
<ForeName>Kevin K</ForeName>
<Initials>KK</Initials>
<AffiliationInfo><Affiliation>Dept of Medicine, National Jewish Health, Denver, CO, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Cadranel</LastName>
<ForeName>Jacques</ForeName>
<Initials>J</Initials>
<AffiliationInfo><Affiliation>Pneumologie, Hopital Tenon, Paris, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Corte</LastName>
<ForeName>Tamera J</ForeName>
<Initials>TJ</Initials>
<AffiliationInfo><Affiliation>The Aldred Hospital, Melbourne, Australia Members of the writing group of the task force.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>du Bois</LastName>
<ForeName>Roland M</ForeName>
<Initials>RM</Initials>
<AffiliationInfo><Affiliation>Interstitial Lung Disease Unit, Dept of Occupational Medicine, Royal Brompton Hospital, London, UK.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Lee</LastName>
<ForeName>Joyce S</ForeName>
<Initials>JS</Initials>
<AffiliationInfo><Affiliation>Medicine, University of California San Francisco, San Francisco, CA, USA Members of the writing group of the task force.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Leslie</LastName>
<ForeName>Kevin O</ForeName>
<Initials>KO</Initials>
<AffiliationInfo><Affiliation>Pathology, Mayo Clinic, Scottsdale, AZ, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Lynch</LastName>
<ForeName>David A</ForeName>
<Initials>DA</Initials>
<AffiliationInfo><Affiliation>Dept of Radiology, National Jewish Health, Denver, CO, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Matteson</LastName>
<ForeName>Eric L</ForeName>
<Initials>EL</Initials>
<AffiliationInfo><Affiliation>Division of Rheumatology, Mayo College of Medicine, Rochester, MN, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Mosca</LastName>
<ForeName>Marta</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>University of Pisa, Pisa, Italy.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Noth</LastName>
<ForeName>Imre</ForeName>
<Initials>I</Initials>
<AffiliationInfo><Affiliation>Medicine, University of Chicago, Chicago, IL, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Richeldi</LastName>
<ForeName>Luca</ForeName>
<Initials>L</Initials>
<AffiliationInfo><Affiliation>Southampton General Hospital, Southampton, UK.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Strek</LastName>
<ForeName>Mary E</ForeName>
<Initials>ME</Initials>
<AffiliationInfo><Affiliation>Medicine, University of Chicago, Chicago, IL, USA Members of the writing group of the task force.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Swigris</LastName>
<ForeName>Jeffrey J</ForeName>
<Initials>JJ</Initials>
<AffiliationInfo><Affiliation>Dept of Medicine, National Jewish Health, Denver, CO, USA Members of the writing group of the task force.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Wells</LastName>
<ForeName>Athol U</ForeName>
<Initials>AU</Initials>
<AffiliationInfo><Affiliation>Interstitial Lung Disease Unit, Royal Brompton Hospital, London, UK.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>West</LastName>
<ForeName>Sterling G</ForeName>
<Initials>SG</Initials>
<AffiliationInfo><Affiliation>University of Colorado School of Medicine, Aurora, CO, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Collard</LastName>
<ForeName>Harold R</ForeName>
<Initials>HR</Initials>
<AffiliationInfo><Affiliation>Medicine, University of California San Francisco, San Francisco, CA, USA Members of the writing group of the task force Task force vice-chairs, and contributed equally to this manuscript.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Cottin</LastName>
<ForeName>Vincent</ForeName>
<Initials>V</Initials>
<AffiliationInfo><Affiliation>Service de Pneumologie, Hopital L. Pradel, Lyon, France Members of the writing group of the task force Task force vice-chairs, and contributed equally to this manuscript.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><CollectiveName>“ERS/ATS Task Force on Undifferentiated Forms of CTD-ILD”</CollectiveName>
</Author>
</AuthorList>
<Language>eng</Language>
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<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
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<ArticleDate DateType="Electronic"><Year>2015</Year>
<Month>07</Month>
<Day>09</Day>
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<MedlineJournalInfo><Country>England</Country>
<MedlineTA>Eur Respir J</MedlineTA>
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<CommentsCorrectionsList><CommentsCorrections RefType="CommentIn"><RefSource>Eur Respir J. 2016 Apr;47(4):1295-6</RefSource>
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<QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName>
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<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
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<MeshHeading><DescriptorName UI="D054988" MajorTopicYN="N">Idiopathic Interstitial Pneumonias</DescriptorName>
<QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName>
<QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName>
<QualifierName UI="Q000628" MajorTopicYN="Y">therapy</QualifierName>
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<MeshHeading><DescriptorName UI="D017563" MajorTopicYN="N">Lung Diseases, Interstitial</DescriptorName>
<QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName>
<QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName>
<QualifierName UI="Q000628" MajorTopicYN="Y">therapy</QualifierName>
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<MeshHeading><DescriptorName UI="D011446" MajorTopicYN="N">Prospective Studies</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D015272" MajorTopicYN="N">Pulmonary Medicine</DescriptorName>
<QualifierName UI="Q000592" MajorTopicYN="Y">standards</QualifierName>
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<MeshHeading><DescriptorName UI="D014481" MajorTopicYN="N" Type="Geographic">United States</DescriptorName>
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