Literature DB >> 183578

Defective lung macrophages in pulmonary alveolar proteinosis.

D W Golde, M Territo, T N Finley, M J Cline.   

Abstract

Lung macrophages obtained by segmental lavage from three patients with pulmonary alveolar proteinosis were studied in vitro. The macrophages exhibited morphologic abnormalities including excessive lipid accumulation and giant secondary lysosome formation. These cells survived poorly in tissue culture, showed impaired chemotactic activity, and had decreased adhesiveness to glass. They phagocytized normally but had substantially decreased capacity to kill ingested Candida pseudotropicalis. Evidence was obtained that the macrophage defect was acquired and probably related to ingestion of the proteinaceous alveolar fluid. Peripheral blood monocyte function was normal in one patient and morphologic abnormalities were produced in normal monocyte-derived macrophages cultured with proteinaceous lavage material. These studies suggest that the lung macrophage in alveolar proteinosis is a defective cell as a consequence of an abnormal pulmonary environment.

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Year:  1976        PMID: 183578     DOI: 10.7326/0003-4819-85-3-304

Source DB:  PubMed          Journal:  Ann Intern Med        ISSN: 0003-4819            Impact factor:   25.391


  31 in total

Review 1.  Pulmonary alveolar proteinosis: clinical aspects and current concepts on pathogenesis.

Authors:  P L Shah; D Hansell; P R Lawson; K B Reid; C Morgan
Journal:  Thorax       Date:  2000-01       Impact factor: 9.139

2.  In vivo studies of rat alveolar macrophage [corrected] microviscosity: influence of pulmonary surfactant synthesis stimulation.

Authors:  M Luisetti; M Salmona; E Pozzi; M Genghini; L Spialtini; P Masturzo
Journal:  Lung       Date:  1987       Impact factor: 2.584

3.  Management of pulmonary alveolar proteinosis by repeated bronchoalveolar lavage.

Authors:  R I Simpson; M A Ramsay; M W Millard; J E Capehart
Journal:  Proc (Bayl Univ Med Cent)       Date:  2000-04

4.  Liquid paraffin pneumonia--with chemical analysis and electronmicroscopy.

Authors:  B Fox
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1979-06-29

5.  The involvement of GM-CSF deficiencies in parallel pathways of pulmonary alveolar proteinosis and the alcoholic lung.

Authors:  William S Slovinsky; Freddy Romero; Dominic Sales; Hoora Shaghaghi; Ross Summer
Journal:  Alcohol       Date:  2018-07-18       Impact factor: 2.405

6.  GM-CSF regulates a PU.1-dependent transcriptional program determining the pulmonary response to LPS.

Authors:  Pierre-Yves Berclaz; Brenna Carey; Marie-Dominique Fillipi; Kara Wernke-Dollries; Nick Geraci; Stephanie Cush; Terry Richardson; Joe Kitzmiller; Michael O'connor; Christina Hermoyian; Thomas Korfhagen; Jeffrey A Whitsett; Bruce C Trapnell
Journal:  Am J Respir Cell Mol Biol       Date:  2006-08-17       Impact factor: 6.914

Review 7.  Secondary alveolar proteinosis in cancer patients.

Authors:  S Ladeb; J Fleury-Feith; E Escudier; J Tran Van Nhieu; J F Bernaudin; C Cordonnier
Journal:  Support Care Cancer       Date:  1996-11       Impact factor: 3.603

8.  Pulmonary interstitial fibrosis associated with alveolar proteinosis.

Authors:  H W Clague; A C Wallace; W K Morgan
Journal:  Thorax       Date:  1983-11       Impact factor: 9.139

9.  Pulmonary alveolar proteinosis: prospective clinical experience in 23 patients for 15 years.

Authors:  K Kariman; J A Kylstra; A Spock
Journal:  Lung       Date:  1984       Impact factor: 2.584

10.  Surfactant protein D. Increased accumulation in silica-induced pulmonary lipoproteinosis.

Authors:  E Crouch; A Persson; D Chang; D Parghi
Journal:  Am J Pathol       Date:  1991-10       Impact factor: 4.307

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