Approaches to assess IgE mediated allergy risks (sensitization and cross reactivity) from new or modified dietary proteins

被引:31
|
作者
Remington, B. [1 ]
Broekman, H. C. H. [2 ]
Blom, W. M. [1 ]
Capt, A. [3 ]
Crevel, R. W. R. [4 ]
Dimitrov, I. [5 ]
Faeste, C. K. [6 ]
Fernandez-Canton, R. [7 ]
Giavi, S. [8 ]
Houben, G. F. [1 ]
Glenn, K. C. [9 ]
Madsen, C. B. [10 ]
Kruizinga, A. K. [1 ]
Constable, A. [11 ]
机构
[1] TNO, Zeist, Netherlands
[2] UMCU, Dept Dermatol Allergol, POB 85500, Utrecht, Netherlands
[3] Bayer SAS, Sophia Antipolis, France
[4] Unilever, Safety & Environm Assurance Ctr, Bedford, England
[5] Med Univ Sofia, Fac Pharm, Sofia 1000, Bulgaria
[6] Norwegian Vet Inst, Oslo, Norway
[7] Monsanto Europe SA, Ave Tervuren 270-272, B-1150 Brussels, Belgium
[8] Univ Athens, Allergy Dept, Paediat Clin 2, Athens, Greece
[9] Monsanto Co, 800 N Lindbergh Blvd, St Louis, MO 63017 USA
[10] Tech Univ Denmark, Natl Food Inst, Soborg, Denmark
[11] Nestec Ltd, POB 44, CH-1000 Lausanne 26, Switzerland
关键词
Allergen; IgE; Sensitization; Risk assessment; Novel proteins; Hazard analysis; CONTROLLED FOOD CHALLENGE; VITRO DIGESTION METHOD; ARA H 2; IN-VITRO; HYPERSENSITIVITY REACTION; ALLERGENICITY ASSESSMENT; LUPIN SENSITIZATION; OBJECTIVE SYMPTOMS; GASTRIC RESIDENCE; ORAL TOLERANCE;
D O I
10.1016/j.fct.2017.12.025
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The development and introduction of new dietary protein sources has the potential to improve food supply sustainability. Understanding the potential allergenicity of these new or modified proteins is crucial to ensure protection of public health. Exposure to new proteins may result in de novo sensitization, with or without clinical allergy, or clinical reactions through cross-reactivity. In this paper we review the potential of current methodologies (in silico, in vitro degradation, in vitro IgE binding, animal models and clinical studies) to address these outcomes for risk assessment purposes for new proteins, and especially to identify and characterise the risk of sensitization for IgE mediated allergy from oral exposure. Existing tools and tests are capable of assessing potential crossreactivity. However, there are few possibilities to assess the hazard due to de novo sensitization. The only methods available are in vivo models, but many limitations exist to use them for assessing risk. We conclude that there is a need to understand which criteria adequately define allergenicity for risk assessment purposes, and from these criteria develop a more suitable battery of tests to distinguish between proteins of high and low allergenicity, which can then be applied to assess new proteins with unknown risks.
引用
收藏
页码:97 / 107
页数:11
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