Lipid-transfer protein is the major maize allergen maintaining IgE-binding activity after cooking at 100°C, as demonstrated in anaphylactic patients and patients with positive double-blind, placebo-controlled food challenge results

被引:76
作者
Pastorello, EA
Pompei, C
Pravettoni, V
Farioli, L
Calamari, AM
Scibilia, J
Robino, AM
Conti, A
Iametti, S
Fortunato, D
Bonomi, S
Ortolani, C
机构
[1] Univ Milan, Osped Maggiore, IRCCS, Div Gen Med 1,Allergy Ctr,Dept Internal Med, Milan, Italy
[2] Univ Milan, Dept Food Sci & Microbiol, Milan, Italy
[3] ICP, CEMOC, UOOML, Milan, Italy
[4] Osped Niguarda Ca Granda, Bizzozzero Div, Milan, Italy
[5] ISPA, Natl Res Council, Turin, Italy
[6] Univ Milan, Dept Agrifood Mol Sci, Milan, Italy
关键词
food anaphylaxis; maize allergy; lipid-transfer protein; thermal treatment; double-blind; placebo-controlled food challenge;
D O I
10.1016/S0091-6749(03)01942-0
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: In a previous study a 9-kd lipid-transfer protein (LTP) was identified as the major allergen of raw maize in a population of 22 anaphylactic patients. However, the stability of this protein in cooked maize is unknown. Objective: We investigated the allergenicity of 5 maize hybrids and its modification after different thermal treatments by using sera from anaphylactic patients and patients with positive double-blind, placebo-controlled food challenges. Methods: Five maize hybrids were extracted by using different methods, obtaining the water-soluble, zein, total zein, glutelin, and total protein fractions. The IgE-binding capacity of the different extracts, both raw and after thermal treatment, was investigated by means of SDS-PAGE immunoblotting. A 9-kd heat-stable allergen was purified by means of HPLC and sequenced. Changes in its secondary structure during and after heating from 25degreesC to 100degreesC were monitored by means of circular dichroism. Results: All raw maize hybrids showed similar protein and IgE-binding profiles. The SDS-PAGE of all the heat-treated hybrids demonstrated a decreased number of stained bands in respect to the raw samples. The IgE immunoblotting demonstrated that the major allergen of the water-soluble, total zein, total protein, and glutelin fractions was a 9-kd protein identified by means of amino acid sequence as an LTP and a subtilisin-chymotrypsin inhibitor (in total zein fraction). The IgE-binding capacity of this 9-kd protein remained unchanged after thermal treatments, even though circular dichroism demonstrated an altered secondary structure. Conclusions: Maize UP maintains its IgE-binding capacity after heat treatment, thus being the most eligible candidate for a causative role in severe anaphylactic reactions to both raw and cooked maize.
引用
收藏
页码:775 / 783
页数:9
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