An official European Respiratory Society/American Thoracic Society research statement: interstitial pneumonia with autoimmune features
An official European Respiratory Society/American Thoracic Society research statement: interstitial pneumonia with autoimmune features
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.
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Fischer, Aryeh
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Antoniou, Katerina M.
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Brown, Kevin K.
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Cadranel, Jacques
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Corte, Tamera J.
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Du Bois, Roland M.
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Lee, Joyce S.
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Leslie, Kevin O.
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Lynch, David A.
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Matteson, Eric L.
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Mosca, Marta
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Noth, Imre
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Richeldi, Luca
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Strek, Mary E.
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Swigris, Jeffrey J.
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Wells, Athol U.
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West, Sterling G.
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Collard, Harold R.
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Cottin, Vincent
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Fischer, Aryeh
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Antoniou, Katerina M.
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Brown, Kevin K.
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Cadranel, Jacques
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Corte, Tamera J.
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Du Bois, Roland M.
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Lee, Joyce S.
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Leslie, Kevin O.
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Lynch, David A.
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Matteson, Eric L.
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Mosca, Marta
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Noth, Imre
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Richeldi, Luca
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Strek, Mary E.
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Swigris, Jeffrey J.
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Wells, Athol U.
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West, Sterling G.
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Collard, Harold R.
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Cottin, Vincent
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Fischer, Aryeh, Antoniou, Katerina M., Brown, Kevin K., Cadranel, Jacques, Corte, Tamera J., Du Bois, Roland M., Lee, Joyce S., Leslie, Kevin O., Lynch, David A., Matteson, Eric L., Mosca, Marta, Noth, Imre, Richeldi, Luca, Strek, Mary E., Swigris, Jeffrey J., Wells, Athol U., West, Sterling G., Collard, Harold R. and Cottin, Vincent
(2015)
An official European Respiratory Society/American Thoracic Society research statement: interstitial pneumonia with autoimmune features.
European Respiratory Journal, 46 (4), .
(doi:10.1183/13993003.00150-2015).
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.
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Accepted/In Press date: 11 May 2015
e-pub ahead of print date: 30 September 2015
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Local EPrints ID: 443448
URI: http://eprints.soton.ac.uk/id/eprint/443448
ISSN: 0903-1936
PURE UUID: 89a63c42-fc40-43d0-9626-3d74ce7d8a60
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Date deposited: 26 Aug 2020 16:34
Last modified: 16 Mar 2024 09:05
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Contributors
Author:
Aryeh Fischer
Author:
Katerina M. Antoniou
Author:
Kevin K. Brown
Author:
Jacques Cadranel
Author:
Tamera J. Corte
Author:
Roland M. Du Bois
Author:
Joyce S. Lee
Author:
Kevin O. Leslie
Author:
David A. Lynch
Author:
Eric L. Matteson
Author:
Marta Mosca
Author:
Imre Noth
Author:
Luca Richeldi
Author:
Mary E. Strek
Author:
Jeffrey J. Swigris
Author:
Athol U. Wells
Author:
Sterling G. West
Author:
Harold R. Collard
Author:
Vincent Cottin
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