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Efficacy of baked milk oral immunotherapy in baked milk–reactive allergic patients - 04/12/15

Doi : 10.1016/j.jaci.2015.05.040 
Michael R. Goldberg, MD, PhD a, , Liat Nachshon, MD a, Michael Y. Appel, PhD a, Arnon Elizur, MD a, b, Michael B. Levy, MD a, Eli Eisenberg, PhD c, Hugh A. Sampson, MD d, Yitzhak Katz, MD a, b
a Allergy and Immunology Institute, Assaf Harofeh Medical Center, Zerifin, Israel 
b Department of Pediatrics, Sackler Faculty of Medicine, New York, NY 
c Raymond and Beverly Sackler School of Physics and Astronomy, Tel Aviv University, Tel Aviv, Israel 
d Elliot and Roslyn Jaffe Food Allergy Institute, Division of Allergy and Immunology, Department of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY 

Corresponding author: Michael R. Goldberg, MD, PhD, Institute of Allergy, Immunology and Pulmonology, Assaf Harofeh Medical Center, Zerifin, 70300, Israel.

Abstract

Background

Patients with IgE-mediated cow's milk allergy who are nonreactive to baked milk (BM) can be desensitized with BM to promote tolerance to unheated milk (UM).

Objective

We sought to test whether patients who are BM reactive can progress in BM oral immunotherapy (OIT) and become desensitized to UM as well.

Methods

Fifteen patients (>4 years) who previously failed to complete our milk OIT program were enrolled into the BM OIT protocol. A dose of BM (180°C for 30 minutes) which was less than the eliciting dose was increased 50% monthly while under medical supervision until the primary outcome dose of 1.3 g/d BM protein was achieved. Basophil reactivity and milk protein–specific IgE binding were analyzed at the first round of BM OIT therapy (T0) and at 12 months of BM treatment.

Results

In terms of the primary outcome, only 3 (21%) of 14 patients tolerated the 1.3 g/d BM dose. Although some patients initially progressed in BM OIT, 8 of 11 failed because of IgE-mediated reactions. Three did not complete the program because of non–IgE-mediated factors. An increase in challenge threshold to UM was noted in patients continuing until 12 months (P = .003), including those among whom reactions precluded continuation in the program. Patients (n = 3) who successfully reached maintenance had decreased milk-specific IgE reactivity. Furthermore, the mean difference at T0 between induced HM and UM percentages of CD203c expression was significantly lower in patients who successfully completed BM OIT than in those who did not (−11% vs 4.4%, P = .0002), which is consistent with their decreased clinical reactivity to BM.

Conclusions

Although use of hypoallergenic BM in OIT is a promising therapy, care must be taken before its administration in BM-reactive patients because of the risk for anaphylaxis and only limited increase in challenge threshold attained.

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Key words : Oral immunotherapy, cow's milk allergy, baked milk

Abbreviations used : BAT, BM, CMP, HM, IgE-CMA, OFC, OIT, UM


Plan


 M.R.G. is supported by a Kamea grant from the Ministry of Health, Israel. Y.K. is supported by the Leon Alcalay Chair in Pediatric Immunology, Tel Aviv University. Research was supported by the Ministry of Health (Chief Scientist Office no. 3-00000-9115) and the Allergists for Israel (AFI).
 Disclosure of potential conflict of interest: M. R. Goldberg has received research support from the Israel Ministry of Health (Chief Scientist Office no. 3-00000-9115) and from Allergists for Israel. L. Nachshon and Y. Katz have received research support from the Israel Ministry of Health. H. A. Sampson has received consultancy fees from Allertein Therapeutics (4% share). The rest of the authors declare that they have no relevant conflicts of interest.
 ClinicalTrials.gov Identifier: NCT01968278.


© 2015  American Academy of Allergy, Asthma & Immunology. Publié par Elsevier Masson SAS. Tous droits réservés.
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Vol 136 - N° 6

P. 1601-1606 - décembre 2015 Retour au numéro
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