Serum IgA and IGg Subclasses During Treatment for Acute Respiratory Exacerbation in Cystic Fibrosis: Analysis of Patients Colonised with Mucoid or Non-Mucoid Strains of Pseudomonas Aeruginosa
- 1 January 1994
- journal article
- research article
- Published by Taylor & Francis in Immunological Investigations
- Vol. 23 (1) , 1-13
- https://doi.org/10.3109/08820139409063428
Abstract
Patients with cystic fibrosis (CF) have a high prevalence of Pseudomonas aeruginosa infection which causes chronic infection of the mucosal surfaces of the lung. This results in recurrent immune stimulation and hypergamma-globulinemia. The present study examines the levels of circulating Ig classes, IgG and IgA subclasses in 13 adult patients with CF during acute pulmonary infection and post-exacerbation. Total serum IgG levels were raised in the patients during infection and post-treatment when compared to the normal range (mean ± SEM: 17.21 ± 1.4 g/l vs 16.45 ± 1.5 g/l respectively; normal range 8 - 16 g/l). In contrast, total IgM (2.6 ± 0.26 vs 2.69 ± 2.74 g/l; normal range 0.6 - 2.8 g/l) and IgA levels (2.5 ± 0.52 vs 2.41 ± 0.48 g/l; normal range 0.5 - 4 g/l) remained unchanged when examined during all stages of the disease. Of the 13 patients studied, 69%, 39% and 31% had IgG, IgM and IgA levels respectively raised above the normal range values. The mean levels of individual IgG subclasses examined in this group of patients revealed values within the normal ranges, however IgG2 and IgG3 were increased in 31% and 46% of patients. Individual IgG3 levels fell in 77% (10/13) and IgG4 in 62% (8/13) of the patients post-exacerbation. With regard to IgA subclasses, significant reduction in the IgAl levels were observed post treatment (3687 ± 539 mg/l vs 2713 ± 498 mg/l, p<0.01). In contrast, IgA2 levels were increased from 279 ± 49 mg/l to 421 ± 69 mg/l, although statistical significance was not reached. Upon antibiotic treatment for infection, the findings in this study show that IgA1 which is susceptible to bacterial proteases is reduced with a concommitant increase in the protease resistant IgA2 subclass. Moreover, patients colonised with non-mucoid strains of P. aeroginosa had higher total IgA levels due to the raised IgAl subclass whereas they had lower IgG levels due to low IgG2 and IgG4 subclasses.Keywords
This publication has 19 references indexed in Scilit:
- Molecular heterogeneity of human IgA antibodies during an immune responseClinical and Experimental Immunology, 1992
- The immunoglobulin G subclass composition of immune complexes in cystic fibrosis. Implications for the pathogenesis of the Pseudomonas lung lesion.Journal of Clinical Investigation, 1990
- Mechanisms of Neutralization of Influenza Virus on Mouse Tracheal Epithelial Cells by Mouse Monoclonal Polymeric IgA and Polyclonal IgM Directed Against the Viral HaemagglutininJournal of General Virology, 1990
- Increased levels of IgG subclasses specific for Pseudomonas aeruginosa exoenzyme and polysaccharide antigens in chronically infected patients with cystic fibrosisAPMIS, 1989
- Natural and Vaccine-Related Immunity to Streptococcus pneumoniaeThe Journal of Infectious Diseases, 1986
- Granulocyte Neutral Proteases and Pseudomonas Elastase as Possible Causes of Airway Damage in Patients with Cystic FibrosisThe Journal of Infectious Diseases, 1984
- IMMUNE COMPLEX MEDIATED TISSUE DAMAGE IN THE LUNGS OF CYSTIC FIBROSIS PATIENTS WITH CHRONIC PSEUDOMONAS AERUGINOSA INFECTIONActa Paediatrica, 1982
- Production of predominantly polymeric IgA by human peripheral blood lymphocytes stimulated in vitro with mitogens.The Journal of Experimental Medicine, 1980
- Pulmonary Host Defenses in Rabbits after Immunization with Pseudomonas Antigens: The Interaction of Bacteria, Antibodies, Macrophages, and LymphocytesThe Journal of Infectious Diseases, 1974
- Immunochemical quantitation of antigens by single radial immunodiffusionImmunochemistry, 1965