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Staphylococcus aureus fibronectin-binding protein specifically binds IgE from patients with atopic dermatitis and requires antigen presentation for cellular immune responses.
- Source :
-
The Journal of allergy and clinical immunology [J Allergy Clin Immunol] 2011 Jul; Vol. 128 (1), pp. 82-91.e8. Date of Electronic Publication: 2011 Apr 21. - Publication Year :
- 2011
-
Abstract
- Background: Staphylococcus aureus superinfections occur in more than 90% of patients with atopic dermatitis (AD) and aggravate skin inflammation. S aureus toxins lead to tissue damage and augment T-cell-mediated skin inflammation by a superantigen effect.<br />Objective: To characterize IgE-reactive proteins from S aureus.<br />Methods: A genomic S aureus library was screened with IgE from patients with AD for DNA clones coding for IgE-reactive antigens. One was identified as fibronectin-binding protein (FBP). Recombinant FBP was expressed in Escherichia coli, purified, and tested for specific IgE reactivity in patients with AD. Its allergenic activity was studied in basophil activation experiments and T-cell cultures. The in vivo allergenic activity was investigated by sensitizing mice.<br />Results: Using IgE from patients with AD for screening of a genomic S aureus library, an IgE-reactive DNA clone was isolated that coded for FBP. Recombinant FBP was expressed in E coli and purified. It reacted specifically with IgE from patients with AD and exhibited allergenic activity in basophil degranulation assays. FBP showed specific T-cell reactivity requiring antigen presentation and induced the secretion of proinflammatory cytokines from PBMCs. Mice sensitized with FBP mounted FBP-specific IgE responses, showed FBP-specific basophil degranulation as well as FBP-specific T-cell proliferation, and mixed T(h)2/T(h)1 cytokine secretion.<br />Conclusion: Evidence is provided that specific humoral and cellular immune responses to S aureus antigens dependent on antigen presentation represent a novel mechanism for S aureus-induced skin inflammation in AD. Furthermore, FBP may be used for the development of novel diagnostic and therapeutic strategies for S aureus infections.<br /> (Copyright © 2011 American Academy of Allergy, Asthma & Immunology. Published by Mosby, Inc. All rights reserved.)
- Subjects :
- Adhesins, Bacterial genetics
Adolescent
Adult
Aged
Amino Acid Sequence
Animals
Base Sequence
Child
Child, Preschool
Dermatitis, Atopic microbiology
Female
Humans
Infant
Male
Mice
Middle Aged
Molecular Sequence Data
Recombinant Proteins immunology
Superantigens immunology
Young Adult
Adhesins, Bacterial immunology
Antigen Presentation immunology
Dermatitis, Atopic immunology
Immunoglobulin E immunology
Staphylococcal Infections immunology
Staphylococcus aureus immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1097-6825
- Volume :
- 128
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- The Journal of allergy and clinical immunology
- Publication Type :
- Academic Journal
- Accession number :
- 21513970
- Full Text :
- https://doi.org/10.1016/j.jaci.2011.02.034