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Blomia tropicalis allergen 5 (Blo t 5) T-cell epitopes and their ability to suppress the allergic immune response.

Authors :
Wong KH
Zhou Q
Prabhu N
Furuhashi K
Chua YL
Grotenbreg GM
Kemeny DM
Source :
Immunology [Immunology] 2017 Oct; Vol. 152 (2), pp. 344-355. Date of Electronic Publication: 2017 Jul 17.
Publication Year :
2017

Abstract

Blomia tropicalis is the major asthma allergen in the tropics comparable to Dermatophagoides pteronyssinus. However, little is known about the B. tropicalis epitopes recognized by T cells. Our aim was to identify the T-cell epitopes in the major B. tropicalis allergen, Blo t 5, and investigate the potential of the corresponding peptides to inhibit the allergic inflammatory lung response. C57BL/6 mice were immunized with plasmid DNA encoding Blo t 5 and T-cell epitopes identified using the interferon-γ ELISPOT assay with 15-mer overlapping peptides. C57BL/6 mice were sensitized with bone-marrow-derived dendritic cells (BMDC) pulsed with Blo t 5 allergen followed by intranasal Blo t 5 challenge. Two H-2 <superscript>b</superscript> restricted epitopes (Bt5 <subscript>76-90</subscript> and Bt5 <subscript>106-115</subscript> ) were recognized by CD4 T cells specific for Blo t 5, but no CD8 epitopes were identified. In mice sensitized with Blo t 5-pulsed BMDC and challenged with intranasal Blo t 5 Bt5 <subscript>76-90</subscript> and Bt5 <subscript>106-115</subscript> , peptide-specific CD4 T cells were found to secrete the T helper type 2 cytokines interleukin-5 and interleukin-13. Intradermal administration of synthetic peptides encoding the identified T-cell epitopes suppressed allergic airway inflammation to further allergen challenges. Hence, we have identified novel CD4 T-cell epitopes specific for Blo t 5 and demonstrated that these peptides could be employed therapeutically to suppress the T-cell response in a murine model of allergic airway inflammation.<br /> (© 2017 John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1365-2567
Volume :
152
Issue :
2
Database :
MEDLINE
Journal :
Immunology
Publication Type :
Academic Journal
Accession number :
28581024
Full Text :
https://doi.org/10.1111/imm.12772