Prevention of allergic asthma by vaccination with transgenic rice seed expressing mite allergen: induction of allergen-specific oral tolerance without bystander suppression

被引:62
作者
Suzuki, Kazuya [1 ,2 ]
Kaminuma, Osamu [1 ]
Yang, Lijun [2 ]
Takai, Toshiro [3 ]
Mori, Akio [4 ]
Umezu-Goto, Makiko [4 ]
Ohtomo, Takayuki [4 ]
Ohmachi, Yasushi [5 ]
Noda, Yuko [5 ]
Hirose, Sakiko [2 ]
Okumura, Ko [3 ]
Ogawa, Hideoki [3 ]
Takada, Kazuko [6 ]
Hirasawa, Masatomo [6 ]
Hiroi, Takachika [1 ]
Takaiwa, Fumio [2 ]
机构
[1] Tokyo Metropolitan Inst Med Sci, Dept Allergy & Immunol, Setagaya Ku, Tokyo, Japan
[2] Natl Inst Agrobiol Sci, Transgen Crop Res & Dev Ctr, Tsukuba, Ibaraki, Japan
[3] Juntendo Univ, Sch Med, Atopy Allergy Res Ctr, Bunkyo Ku, Tokyo 113, Japan
[4] Sagamihara Natl Hosp, Natl Hosp Org, Clin Res Ctr Allergy & Rheumatol, Sagamihara, Kanagawa, Japan
[5] Natl Inst Radiol Sci, Dept Adv Technol Radiat Protect Res, Chiba 260, Japan
[6] Nihon Univ, Dept Oral Microbiol, Sch Dent Matsudo, Matsudo, Chiba, Japan
关键词
bronchial asthma; bystander suppression; edible vaccine; house dust mite; immunotherapy; transgenic plant; REGULATORY T-CELL; EDIBLE VACCINE; PROTEIN BODIES; IGE; EPITOPES; DER-P-1; IMMUNOTHERAPY; RESPONSES; PEPTIDE; ANTIGENS;
D O I
10.1111/j.1467-7652.2011.00613.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
This study tested the feasibility of oral immunotherapy for bronchial asthma using a newly developed subunit vaccine in which a fragment (p45-145) of mite allergen (Der p 1) containing immunodominant human and mouse T cell epitopes was encapsulated in endoplasmic reticulum-derived protein bodies of transgenic (Tg) rice seed. Allergen-specific serum immunoglobulin responses, T cell proliferation, Th1/Th2 cytokine production, airway inflammatory cell infiltration, bronchial hyper-responsiveness (BHR) and lung histology were investigated in allergen-immunized and -challenged mice. Prophylactic oral vaccination with the Tg rice seeds clearly reduced the serum levels of allergen-specific IgE and IgG. Allergen-induced CD4(+) T cell proliferation and production of Th2 cytokines in vitro, infiltration of eosinophils, neutrophils and mononuclear cells into the airways and BHR were also inhibited by oral vaccination. The effects of the vaccine were antigen-specific immune response because the levels of specific IgE and IgG in mice immunized with Der f 2 or ovalbumin were not significantly suppressed by oral vaccination with the Der p 1 expressing Tg rice. Thus, the vaccine does not induce nonspecific bystander suppression, which has been a problem with many oral tolerance regimens. These results suggest that our novel vaccine strategy is a promising approach for allergen-specific oral immunotherapy against allergic diseases including bronchial asthma.
引用
收藏
页码:982 / 990
页数:9
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