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[Lung disease in adult common variable immunodeficiency].

AbstractINTRODUCTION:
Common variable immunodeficiency (CVID) is characterized by a defect in antibody production and may be complicated by infectious or non-infectious respiratory disease.
BACKGROUND:
In addition to recurrent infectious complications, mainly due to encapsulated bacteria, CVID may be complicated by diffuse infiltrative, non-infectious lung disease. The latter may be related to granulomatosis, lymphoid interstitial pneumonia, follicular bronchiolitis, follicular nodular hyperplasia, organizing pneumonia or lymphoma. Different lymphoid histological lesions can co-exist and form a new entity called GLILD (granulomatous lymphocytic interstitial lung disease), which is associated with a poor prognosis. Replacement of immunoglobulins significantly decreases the frequency and severity of infections but has no impact on the non-infectious complications.
OUTLOOK:
Studies are needed to determine the modalities of follow-up and better understand the long-term progress of GLILD. These studies should improve the management of GLILD in the context of immunosuppressive treatments, which increase the risk of infection in CVID.
CONCLUSION:
The identification of GLILD, which reflects a variable histological spectrum, rather than a well-defined entity, necessitates revising the approach to diffuse infiltrative lung diseases in CVID.
AuthorsJ Hadjadj, M Malphettes, C Fieschi, E Oksenhendler, A Tazi, A Bergeron
JournalRevue des maladies respiratoires (Rev Mal Respir) Vol. 32 Issue 10 Pg. 991-1001 (Dec 2015) ISSN: 1776-2588 [Electronic] France
Vernacular TitleAtteintes respiratoires au cours du déficit immunitaire commun variable de l'adulte.
PMID26071128 (Publication Type: Journal Article, Review)
CopyrightCopyright © 2015 SPLF. Published by Elsevier Masson SAS. All rights reserved.
Topics
  • Adult
  • Common Variable Immunodeficiency (complications)
  • Humans
  • Lung Diseases (diagnosis, etiology)
  • Lung Diseases, Interstitial (etiology)

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