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Editorial
. 2021 Jul 8:12:699126.
doi: 10.3389/fimmu.2021.699126. eCollection 2021.

Editorial: Interstitial Lung Disease in Primary Immunodeficiencies

Børre Fevang  1   2   3 , Klaus Warnatz  4   5 , John R Hurst  6
Affiliations
Editorial

Editorial: Interstitial Lung Disease in Primary Immunodeficiencies

Børre Fevang et al. Front Immunol. .
No abstract available

Keywords: APECED; Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy; common variable immune deficiency (CVID); granulomatous lymphocytic interstitial lung disease (GLILD); interstitial lung disease (ILD); primary immunodeficencies (PID).

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
(GL) ILD in CVID is characterized by clinical, radiological and histopathological features with patients presenting all or some of these manifestations. Which criteria to include for the diagnosis demands an imminent debate (4).
See this image and copyright information in PMC

Comment on

  • Editorial on the Research Topic Interstitial Lung Disease in Primary Immunodeficiencies

References

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    1. Bates CA, Ellison MC, Lynch DA, Cool CD, Brown KK, Routes JM. Granulomatous-Lymphocytic Lung Disease Shortens Survival in Common Variable Immunodeficiency. J Allergy Clin Immunol (2004) 114:415–21. 10.1016/j.jaci.2004.05.057 - DOI - PubMed
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    1. Hurst JR, Verma N, Lowe D, Baxendale HE, Jolles S, Kelleher P, et al. British Lung Foundation/United Kingdom Primary Immunodeficiency Network Consensus Statement on the Definition, Diagnosis, and Management of Granulomatous-Lymphocytic Interstitial Lung Disease in Common Variable Immunodeficiency Disorders. J Allergy Clin Immunol Pract (2017) 5:938–45. 10.1016/j.jaip.2017.01.021 - DOI - PubMed

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