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Correction to: Nature Immunology https://doi.org/10.1038/s41590-024-01975-x, published online 4 October 2024. In the version of this article initially published, there was a typographical error in the first paragraph of the Methods, where in the sentence now reading “Subsequent CT scans were obtained in 29 patients a median of 118 d (range 31–249 d) after the first CT scan,” the median was first reported as “11 d.” The error has been corrected in the HTML and PDF versions of the article.
Keywords interstitial lung disease 129Xe MRI chronic hypersensitivity pneumonitis high-resolution computed tomography INTRODUCTION The spectrum of fibrotic interstitial lung diseases (ILDs) is characterized by inflammation and scarring of the lung parenchyma, which can lead to end-stage fibrosis. The significant heterogeneity in ILDs presents challenges in differentiating chronic hypersensitivity pneumonitis (CHP) from other fibrotic ILDs, specifically idiopathic pulmonary fibrosis (IPF) [1,2].
Abstract Monocyte-derived alveolar macrophages drive lung injury and fibrosis in murine models and are associated with pulmonary fibrosis in humans. Monocyte-derived alveolar macrophages have been suggested to develop a phenotype that promotes lung repair as injury resolves.
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