Abstract
A major problem with allergen-specific immunotherapy involving repeated injections of allergens is the risk of an anaphylactic reaction. We engineered the major house dust mite allergen, Der f 2, to reduce its capacity to induce skin test reactivity and histamine release from peripheral blood basophils in allergic patients. The engineered allergen, in which the disulfide bond that linked the N- and C-terminal sequences of Der f 2 was disrupted, retained T-cell epitopes essential for immunotherapy and ability to stimulate T-cell proliferation. Such engineered allergens are potentially useful for safer and more effective immunotherapy for allergies.
Original language | English |
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Pages (from-to) | 754-758 |
Number of pages | 5 |
Journal | Nature Biotechnology |
Volume | 15 |
Issue number | 8 |
DOIs | |
Publication status | Published - Aug 1997 |
Keywords
- Allergen engineering
- Immunotherapy
- Protein design
- T-cell proliferation