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Blomia tropicalis allergen 5 (Blo t 5) T-cell epitopes and their ability to suppress the allergic immune response.
Wong, Kenneth H; Zhou, Qian; Prabhu, Nayana; Furuhashi, Kazuki; Chua, Yen Leong; Grotenbreg, Gijsbert M; Kemeny, David M.
Afiliación
  • Wong KH; Immunology Programme, Life Sciences Institute, Centre for Life Sciences, National University of Singapore, Singapore City, Singapore.
  • Zhou Q; Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore City, Singapore.
  • Prabhu N; Immunology Programme, Life Sciences Institute, Centre for Life Sciences, National University of Singapore, Singapore City, Singapore.
  • Furuhashi K; Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore City, Singapore.
  • Chua YL; Immunology Programme, Life Sciences Institute, Centre for Life Sciences, National University of Singapore, Singapore City, Singapore.
  • Grotenbreg GM; Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore City, Singapore.
  • Kemeny DM; Immunology Programme, Life Sciences Institute, Centre for Life Sciences, National University of Singapore, Singapore City, Singapore.
Immunology ; 152(2): 344-355, 2017 10.
Article en En | MEDLINE | ID: mdl-28581024
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-2b restricted epitopes (Bt576-90 and Bt5106-115 ) 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 Bt576-90 and Bt5106-115 , 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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Péptidos / Neumonía / Asma / Alérgenos / Linfocitos T CD4-Positivos / Antiasmáticos / Vacunas de ADN / Ácaros / Epítopos Límite: Animals Idioma: En Revista: Immunology Año: 2017 Tipo del documento: Article País de afiliación: Singapur

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Péptidos / Neumonía / Asma / Alérgenos / Linfocitos T CD4-Positivos / Antiasmáticos / Vacunas de ADN / Ácaros / Epítopos Límite: Animals Idioma: En Revista: Immunology Año: 2017 Tipo del documento: Article País de afiliación: Singapur