4.5 Article

Induction of tolerance after establishment of peanut allergy by the food allergy herbal formula-2 is associated with up-regulation of interferon-γ

期刊

CLINICAL AND EXPERIMENTAL ALLERGY
卷 37, 期 6, 页码 846-855

出版社

WILEY
DOI: 10.1111/j.1365-2222.2007.02718.x

关键词

chinese herbal medicine formula; peanut anaphylaxis; Th-2 cytokine modulation

资金

  1. NCCIH NIH HHS [AT001495] Funding Source: Medline

向作者/读者索取更多资源

Background Peanut (PN)-anaphylaxis is potentially life threatening. We previously reported that a Chinese herbal medicine preparation, food allergy herbal formula-2 (FAEF-2), prevented peanut allergy (PNA) in mice when administered during sensitization. Objective To investigate whether FAFIF-2 also can prevent anaphylactic reactions administered to mice with established PNA and, if so, whether protection would persist after cessation of therapy. Methods C3H/HeJ mice sensitized and boosted over 8 weeks with a standard protocol known to establish PN hypersensitivity received seven weeks of FAHF-2 treatment or water as a sham treatment. Mice were subsequently challenged with PN at week 14 (1-day post-therapy) and week 18 (4-week post-therapy) to evaluate the efficacy and persistence of FAEF-2 treatment by assessing anaphylactic scores, core body temperatures and plasma histamine levels. Serum PN-specific antibody levels and cytokine profiles from splenocytes and mesenteric lymph node (MLN) cells were also determined. Results All sham-treated mice challenged at weeks 14 and 18 showed anaphylactic symptoms. In contrast, FAEF-2-treated mice showed no sign of anaphylactic reactions. PN-specific IgE levels in FAHF-2-treated mice also were reduced whereas IgG2a levels were increased. Furthermore, MLN cells from FAHF-2-treated mice produced markedly less IL-4 and IL-5, but more IFN-gamma, and contained increased numbers of IFN-gamma-producing CD8(+) cells as compared with sham-treated mice. Conclusion FAHF-2 treatment established PN tolerance in this model, which persisted for at least 4-week post-treatment. This result was associated with modulation of intestinal T helper type 1 cell (Th 1) and Th2 cytokine production, and with increased numbers of mesenteric IFN-gamma-producing CD8(+) cells.

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