Oral administration of IL-12 suppresses anaphylactic reactions in a murine model of peanut hypersensitivity

被引:72
作者
Lee, SY [1 ]
Huang, CK
Zhang, TF
Schofield, BH
Burks, AW
Bannon, GA
Sampson, HA
Li, XM
机构
[1] CUNY Mt Sinai Sch Med, Dept Pediat, New York, NY 10029 USA
[2] Johns Hopkins Med Inst, Sch Hyg & Publ Hlth, Dept Environm Hlth Sci, Baltimore, MD 21205 USA
[3] Univ Arkansas, Sch Med, Dept Pediat, Little Rock, AR 72205 USA
[4] Univ Arkansas, Sch Med, Dept Biochem & Mol Biol, Little Rock, AR 72205 USA
关键词
peanut hypersensitivity; IL-12; animal model;
D O I
10.1006/clim.2001.5122
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
There is no satisfactory therapeutic intervention for peanut allergy, which accounts for most life-threatening food allergic reactions. Since IL-12 has been found to inhibit allergic airway responses in a mouse model of asthma and to cure Th2 cytokine-mediated murine schistosomiasis, we hypothesized that IL-12 treatment might also inhibit peanut allergic reactions. Consequently, we investigated the effects of oral IL-12 treatment in a murine model of peanut allergy and found that oral administration of liposome encapsulated rIL-12 could both prevent and reverse peanut hypersensitivity and could reduce histamine release, peanut-specific serum IgE and IgG1, and fecal IgA levels. Oral IL-12 treatment also increased IFN-gamma but did not decrease IL-4 or IL-5 levels. We conclude that oral rIL-12 treatment has therapeutic as well as preventive effects on peanut allergy, which are associated with increased IFN-gamma production. (C) 2001 Academic Press.
引用
收藏
页码:220 / 228
页数:9
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