Title of article :
Heat stability, its measurement, and its lack of utility in the assessment of the potential allergenicity of novel proteins
Author/Authors :
Privalle، نويسنده , , Laura and Bannon، نويسنده , , Gary and Herman، نويسنده , , Rod and Ladics، نويسنده , , Gregory and McCLain، نويسنده , , Scott M. Stagg، نويسنده , , Nicola and Ward، نويسنده , , Jason and Herouet-Guicheney، نويسنده , , Corinne، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2011
Pages :
4
From page :
292
To page :
295
Abstract :
Thermal stability has been reported as a shared characteristic among some of the major food allergens and appears to have originated from the observation that some cooked foods retain their ability to cause allergic reactions by Immunoglobulin E (IgE) binding and the subsequent cascade of events that mediate allergic reactions. Based on this observation, the thermal stability of novel food proteins, like those in transgenic crops, is considered correlative with allergenic risk and has prompted requests from some regulatory agencies for additional testing to address safety concerns. Because human testing and serum IgE screening are not feasible nor are they necessarily useful for evaluating the thermal stability of a novel food protein, a protein function assay is often used to assess the thermal stability in the context of an allergenicity risk assessment. Some regulatory authorities also require immunodetection using polyclonal IgG antibodies and gel based methods. Here we review why heat stability as measured by these functional and immunodetection assays does not correlate with allergenicity and provides no useful safety information in assessing the allergenic potential of novel food proteins.
Keywords :
Transgenic crops , GM crops , Allergenicity , thermal , Regulatory , stability , Lability , Heat
Journal title :
Regulatory Toxicology and Pharmacology
Serial Year :
2011
Journal title :
Regulatory Toxicology and Pharmacology
Record number :
1489459
Link To Document :
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