Hypersensitivity Pneumonitis: Diagnostic and Therapeutic Challenges

Hypersensitivity pneumonitis (HP) is one of the most common interstitial lung diseases (ILD), that presents unique challenges for a confident diagnosis and limited therapeutic options. The disease is triggered by exposure to a wide variety of inciting antigens in susceptible individuals which result...

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Main Authors: Maria Laura Alberti, Emily Rincon-Alvarez, Ivette Buendia-Roldan, Moises Selman
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-09-01
Series:Frontiers in Medicine
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fmed.2021.718299/full
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spelling doaj-ec49eacbeaca4b03bcdcda968aee33892021-09-23T05:54:54ZengFrontiers Media S.A.Frontiers in Medicine2296-858X2021-09-01810.3389/fmed.2021.718299718299Hypersensitivity Pneumonitis: Diagnostic and Therapeutic ChallengesMaria Laura Alberti0Emily Rincon-Alvarez1Ivette Buendia-Roldan2Moises Selman3Hospital María Ferrer, Buenos Aires, ArgentinaFundación Neumológica Colombiana, Bogotá, ColombiaInstituto Nacional de Enfermedades Respiratorias “Ismael Cosío Villegas”, Mexico City, MexicoInstituto Nacional de Enfermedades Respiratorias “Ismael Cosío Villegas”, Mexico City, MexicoHypersensitivity pneumonitis (HP) is one of the most common interstitial lung diseases (ILD), that presents unique challenges for a confident diagnosis and limited therapeutic options. The disease is triggered by exposure to a wide variety of inciting antigens in susceptible individuals which results in T-cell hyperactivation and bronchioloalveolar inflammation. However, the genetic risk and the pathogenic mechanisms remain incompletely elucidated. Revised diagnostic criteria have recently been proposed, recommending to classify the disease in fibrotic and non-fibrotic HP which has strong therapeutic and outcome consequences. Confident diagnosis depends on the presence of clinical features of ILD, identification of the antigen(s), typical images on high-resolution computed tomography (HRCT), characteristic histopathological features, and lymphocytosis in the bronchoalveolar lavage. However, identifying the source of antigen is usually challenging, and HRCT and histopathology are often heterogeneous and not typical, supporting the notion that diagnosis should include a multidisciplinary assessment. Antigen removal and treating the inflammatory process is crucial in the progression of the disease since chronic persistent inflammation seems to be one of the mechanisms leading to lung fibrotic remodeling. Fibrotic HP has a few therapeutic options but evidence of efficacy is still scanty. Deciphering the molecular pathobiology of HP will contribute to open new therapeutic avenues and will provide vital insights in the search for novel diagnostic and prognostic biomarkers.https://www.frontiersin.org/articles/10.3389/fmed.2021.718299/fulllung fibrosisrisk factorshypersensitivity pneumonitisprognostic factorsdiagnosis
collection DOAJ
language English
format Article
sources DOAJ
author Maria Laura Alberti
Emily Rincon-Alvarez
Ivette Buendia-Roldan
Moises Selman
spellingShingle Maria Laura Alberti
Emily Rincon-Alvarez
Ivette Buendia-Roldan
Moises Selman
Hypersensitivity Pneumonitis: Diagnostic and Therapeutic Challenges
Frontiers in Medicine
lung fibrosis
risk factors
hypersensitivity pneumonitis
prognostic factors
diagnosis
author_facet Maria Laura Alberti
Emily Rincon-Alvarez
Ivette Buendia-Roldan
Moises Selman
author_sort Maria Laura Alberti
title Hypersensitivity Pneumonitis: Diagnostic and Therapeutic Challenges
title_short Hypersensitivity Pneumonitis: Diagnostic and Therapeutic Challenges
title_full Hypersensitivity Pneumonitis: Diagnostic and Therapeutic Challenges
title_fullStr Hypersensitivity Pneumonitis: Diagnostic and Therapeutic Challenges
title_full_unstemmed Hypersensitivity Pneumonitis: Diagnostic and Therapeutic Challenges
title_sort hypersensitivity pneumonitis: diagnostic and therapeutic challenges
publisher Frontiers Media S.A.
series Frontiers in Medicine
issn 2296-858X
publishDate 2021-09-01
description Hypersensitivity pneumonitis (HP) is one of the most common interstitial lung diseases (ILD), that presents unique challenges for a confident diagnosis and limited therapeutic options. The disease is triggered by exposure to a wide variety of inciting antigens in susceptible individuals which results in T-cell hyperactivation and bronchioloalveolar inflammation. However, the genetic risk and the pathogenic mechanisms remain incompletely elucidated. Revised diagnostic criteria have recently been proposed, recommending to classify the disease in fibrotic and non-fibrotic HP which has strong therapeutic and outcome consequences. Confident diagnosis depends on the presence of clinical features of ILD, identification of the antigen(s), typical images on high-resolution computed tomography (HRCT), characteristic histopathological features, and lymphocytosis in the bronchoalveolar lavage. However, identifying the source of antigen is usually challenging, and HRCT and histopathology are often heterogeneous and not typical, supporting the notion that diagnosis should include a multidisciplinary assessment. Antigen removal and treating the inflammatory process is crucial in the progression of the disease since chronic persistent inflammation seems to be one of the mechanisms leading to lung fibrotic remodeling. Fibrotic HP has a few therapeutic options but evidence of efficacy is still scanty. Deciphering the molecular pathobiology of HP will contribute to open new therapeutic avenues and will provide vital insights in the search for novel diagnostic and prognostic biomarkers.
topic lung fibrosis
risk factors
hypersensitivity pneumonitis
prognostic factors
diagnosis
url https://www.frontiersin.org/articles/10.3389/fmed.2021.718299/full
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AT emilyrinconalvarez hypersensitivitypneumonitisdiagnosticandtherapeuticchallenges
AT ivettebuendiaroldan hypersensitivitypneumonitisdiagnosticandtherapeuticchallenges
AT moisesselman hypersensitivitypneumonitisdiagnosticandtherapeuticchallenges
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