Characterization of Anaphylaxis After Ecallantide Treatment of Hereditary Angioedema Attacks

被引:32
作者
Craig, Timothy J. [1 ]
Li, H. Henry [2 ]
Riedl, Marc [3 ]
Bernstein, Jonathan A. [4 ]
Lumry, William R. [5 ]
MacGinnitie, Andrew J. [6 ]
Stolz, Leslie E. [7 ]
Biedenkapp, Joseph [7 ]
Chyung, Yung [7 ]
机构
[1] Penn State Univ, Dept Med & Pediat, Hershey, PA 17033 USA
[2] Inst Asthma & Allergy, Chevy Chase, MD USA
[3] Univ Calif San Diego, US Hereditary Angioedema Assoc, Angioedema Ctr, Allergy & Immunol, San Diego, CA 92103 USA
[4] Univ Cincinnati, Coll Med, Dept Internal Med, Div Immunol Allergy, Cincinnati, OH USA
[5] Allergy & Asthma Specialists, Dallas, TX USA
[6] Boston Childrens Hosp, Div Immunol, Boston, MA USA
[7] Dyax Corp, Burlington, MA USA
关键词
Hypersensitivity; Anaphylaxis; Allergy; Hereditary angioedema; Ecallantide; HAE; MANAGEMENT; BRADYKININ; INHIBITOR; SYMPTOMS; ALLERGY;
D O I
10.1016/j.jaip.2014.09.001
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
BACKGROUND: Ecallantide is a human plasma kallikrein inhibitor indicated for treatment of acute attacks of hereditary angioedema for patients 12 years of age and older. Ecallantide is produced in Pichia pastoris yeast cells by recombinant DNA technology. Use of ecallantide has been associated with a risk of hypersensitivity reactions, including anaphylaxis. OBJECTIVE: The objective of this detailed retrospective data review was to characterize anaphylaxis cases within the ecallantide clinical trials database. METHODS: Potential cases of hypersensitivity reactions in the ecallantide clinical development program were identified by examining reported adverse events. The National Institute of Allergy and Infectious Disease criteria were used to identify those events that were consistent with anaphylaxis; these cases were then reviewed in detail. Results from investigational antibody testing also were examined. RESULTS: Among patients who received subcutaneous ecallantide (n = 230 patients; 1045 doses of 30 mg ecallantide), 8 patients (3.5%) had reactions that met the National Institute of Allergy and Infectious Disease criteria for anaphylaxis; none occurred on first exposure to the drug. All 8 reactions had symptom onset within 1 hour of exposure and cutaneous manifestations commonly observed in type I hypersensitivity reactions. All the reactions responded to standard management of type I hypersensitivity reactions and resolved without fatal outcomes. IgE antibody testing to ecallantide or P pastoris was not consistently positive in patients who experienced apparent type I hypersensitivity reactions. CONCLUSION: Anaphylaxis episodes after subcutaneous ecallantide exposure have clinical features suggestive of type I hypersensitivity reactions. However, anti-ecallantide or antie-P pastoris IgE antibody status was not found to be reliably associated with anaphylaxis. (C) 2014 The Authors. Published by Elsevier Inc. on behalf of the American Academy of Allergy, Asthma & Immunology.
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页码:206 / +
页数:11
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