B‐FAHF‐2 plus oral immunotherapy (OIT) is safer and more effective than OIT alone in a murine model of concurrent peanut/tree nut allergy. Issue 8 (15th May 2017)

• Record Type: Journal Article
• Authors: Srivastava, K. D.; Song, Y.; Yang, N.; Liu, C.; Goldberg, I. E.; Nowak‐Węgrzyn, A.; Sampson, H. A.; Li, X.‐M.
• Is Part Of: Clinical & experimental allergy. Volume 47:Issue 8(2017)
• Page Start: 1038
• Page End: 1049
• Publication Date: 2017-05-15
• Subjects: B‐FAHF‐2 -- Chinese herbal medicine -- cytokines and epigenetic regulation -- Food allergies -- murine model of peanut allergies and tree nut allergies -- oral immunotherapy; Allergy -- Periodicals; Immunology -- Periodicals; 616.97
• DOI: 10.1111/cea.12936
• Languages: English
• ISSNs: 0954-7894

Abstract

Summary: Background: Concurrent sensitization to peanut (PN) and tree nuts (TN), the most dangerous food allergies, is common. Current oral immunotherapy (OIT) is not fully satisfactory. Objective: To determine whether the herbal formula B‐FAHF‐2 (BF2) ameliorates PN/TN OIT adverse reactions and enhances persistence of a tolerant state. Methods: Concurrently sensitized PN‐, walnut‐ (WN) and cashew (CSH)‐allergic mice received 1‐day PN/WN/CSH rush OIT plus 3 weeks of maintenance dosing, with or without 3 weeks prior and 3 weeks BF2 co‐treatment. Anaphylactic symptom scores, core body temperatures, plasma histamine levels, basophil numbers, antigen‐specific IgE, cytokine levels, and IL‐4, INF‐γ and Foxp3 gene promoter DNA methylation status, and their correlation with final challenge symptom scores were determined. Results: BF2+OIT‐treated mice experienced significantly fewer and less severe adverse reactions than OIT‐only‐treated mice ( P <.01) during the 1‐day rush OIT build‐up dose phase. Both OIT‐only and BF2+OIT mice showed significant desensitization ( P <.01 and .001, respectively) at 1 week post‐therapy challenge, being greater in BF2+OIT mice. All sham‐treated and 91% of OIT‐treated mice experienced anaphylaxis whereas only 21% of BF2+OIT‐treated mice exhibited reactions during 5‐6 weeks of dose escalation single PN and TN challenges. Greater and more persistent protection in BF2+OIT mice was associated with significantly lower plasma histamine and IgE levels, increased IFN‐γ/IL‐4 and IL‐10/IL‐4 ratios, DNA remethylation at the IL‐4 promoter and demethylation at IFN‐γ and Foxp3 promoters. Final challenge symptom scores were inversely correlated with IL‐4 DNA methylation levels ( P <.0002) and positively correlated with IFN‐γ and Foxp3 gene promoter methylation levels ( P <.0011) ( P <.0165). Conclusions and Clinical Relevance: Combined BF2/OIT therapy was safer and produced longer post‐treatment protection and more tolerance‐prone immunological and epigenetic modifications than OIT alone. BF2/OIT may provide an additional OIT option for patients with concurrent PN/TN and other food allergies.