Does a primary host defense abnormality involving monocytes-macrophages underlie the pathogenesis of lung disease in cystic fibrosis?
- 1 May 1982
- journal article
- Published by Elsevier in Medical Hypotheses
- Vol. 8 (5) , 527-542
- https://doi.org/10.1016/0306-9877(82)90014-7
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Phagocytosis of Candida albicans by alveolar macrophages from patients with cystic fibrosisClinical Immunology and Immunopathology, 1982
- Impaired beta adrenergic receptor binding and function in cystic fibrosis neutrophils.Journal of Clinical Investigation, 1981
- Synthesis and Secretion of Cystic Fibrosis Ciliary Dyskinesia Substances by Purified Subpopulations of LeukocytesJournal of Clinical Investigation, 1980
- Increased binding of concanavalin a to α2-macroglobulin, IgM and IgG from cystic fibrosis plasmaBiochemical and Biophysical Research Communications, 1980
- Hypogammaglobulinemia in Patients with Cystic FibrosisNew England Journal of Medicine, 1980
- Cystic fibrosis α2-macroglobulin protease interaction in vitroClinica Chimica Acta; International Journal of Clinical Chemistry, 1980
- Biological activities of cystic fibrosis serum III. CF serum induced uptake of 45Ca++ by rabbit tracheal explantsBiochemical and Biophysical Research Communications, 1979
- Alpha-2 macroglobulin-enzyme complexes as suppressors of cellular activityCellular Immunology, 1978
- Enhancement of udpgalactose: Glycoprotein galactosyltransferase in cultured human skin fibroblasts by cationic polypeptidesBiochimica et Biophysica Acta (BBA) - General Subjects, 1978
- CYSTIC FIBROSIS HETEROZYGOSITY IN PATHOGENESIS OF ALLERGYThe Lancet, 1976