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1.
Clin Exp Allergy ; 39(9): 1427-37, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19624524

ABSTRACT

BACKGROUND: Plant food allergy in the Mediterranean area is mainly caused by non-specific lipid transfer proteins (nsLTP). The aim of this study was to characterize peanut nsLTP in comparison with peach nsLTP, Pru p 3, and assess its importance in peanut allergy. METHODS: Peanut-allergic patients from Spain (n=32) were included on the basis of a positive case history and either a positive skin prick test or specific IgE to peanut. For comparison, sera of 41 peanut-allergic subjects from outside the Mediterranean area were used. Natural Ara h 9 and two isoforms of recombinant Ara h 9, expressed in Pichia pastoris, were purified using a two-step chromatographic procedure. Allergen characterization was carried out by N-terminal sequencing, circular dichroism (CD) spectroscopy, immunoblotting, IgE inhibition tests and basophil histamine release assays. RESULTS: Compared with natural peanut nsLTP, the recombinant proteins could be purified in high amounts from yeast supernatant (> or =45 mg/L). The identity of the proteins was verified by N-terminal amino acid sequencing and with rabbit nsLTP-specific antibodies. CD spectroscopy revealed similar secondary structures for all preparations and Pru p 3. The Ara h 9 isoforms showed 62-68% amino acid sequence identity with Pru p 3. IgE antibody reactivity to rAra h 9 was present in 29/32 Spanish and 6/41 non-Mediterranean subjects. Recombinant Ara h 9 showed strong cross-reactivity to nPru p 3 and similar IgE-binding capacity as nAra h 9. The two Ara h 9 isoforms displayed similar IgE reactivity. In peanut-allergic patients with concomitant peach allergy, Ara h 9 showed a weaker allergenic potency than Pru p 3 in histamine release assays. CONCLUSIONS: Ara h 9 is a major allergen in peanut-allergic patients from the Mediterranean area. Ara h 9 is capable of inducing histamine release from basophils, but to a lesser extent than Pru p 3.


Subject(s)
Allergens/immunology , Antigens, Plant/immunology , Basophils/immunology , Carrier Proteins/immunology , Glycoproteins/immunology , Histamine/immunology , Immunoglobulin E/immunology , Peanut Hypersensitivity/immunology , Plant Proteins/immunology , Allergens/chemistry , Allergens/pharmacology , Animals , Antigens, Plant/chemistry , Antigens, Plant/pharmacology , Carrier Proteins/chemistry , Carrier Proteins/pharmacology , Circular Dichroism , Female , Glycoproteins/chemistry , Glycoproteins/pharmacology , Humans , Immunoglobulin E/blood , Male , Peanut Hypersensitivity/blood , Plant Proteins/chemistry , Plant Proteins/pharmacology , Protein Isoforms/chemistry , Protein Isoforms/immunology , Protein Isoforms/pharmacology , Protein Structure, Secondary , Rabbits , Recombinant Proteins/chemistry , Recombinant Proteins/immunology , Recombinant Proteins/pharmacology , Spain , Structural Homology, Protein
2.
Clin Exp Allergy ; 37(2): 261-9, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17250699

ABSTRACT

BACKGROUND: An association between plane tree pollen allergy and plant food allergy has been described, but the cross-reacting allergens have not yet been identified. The aim of this study was the identification of homologous non-specific lipid-transfer proteins (nsLTPs) in plane pollen, and to investigate its immunological relationship with the peach LTP, Pru p 3. METHODS: Three different patient groups were recruited in Spain: 22 plane pollen-allergic patients without food allergy (A), 36 plane pollen-allergic patients with peach allergy (B) and 10 peach-allergic patients without plane pollen allergy (C). Proteins from plane pollen extract were fractionated by ion-exchange and reversed-phase chromatography. Further methods applied were N-terminal amino acid sequence analysis, immunoblotting, enzyme allergosorbent test, CAP and basophil histamine release assays. RESULTS: A 10 kDa IgE-reactive protein was purified from plane pollen and identified as nsLTP. Pla a 3 was characterized as a minor allergen (27.3%) in plane pollen-allergic patients without food allergy (A) and as a major allergen in plane pollen-allergic patients with peach allergy (B) showing a prevalence of IgE-reactivity of 63.8%. Group B contained patients sensitized to Pru p 3 without IgE-reactivity to plane-LTP (16.6%). By contrast, Pla a 3 IgE-reactive patients without sensitization to Pru p 3 could be found (16.6%). The sera of patients sensitized to both LTPs (50%), Pla a 3 and Pru p 3, showed different biological activity in histamine release assay: depending on individual patient's sera tested, Pla a 3 showed a similar, a stronger or a weaker allergenic potency in comparison with Pru p 3. CONCLUSIONS: Plane LTP is a major allergen in plane pollen-allergic patients with peach allergy recruited in the Mediterranean area. The results of histamine release tests and different IgE-binding profiles pointed towards the existence of species-specific IgE epitopes. Likewise, no general conclusion on the sensitizer could be made.


Subject(s)
Antigens, Plant/immunology , Carrier Proteins/immunology , Food Hypersensitivity/immunology , Plant Proteins/immunology , Prunus/immunology , Rhinitis, Allergic, Seasonal/immunology , Trees/immunology , Allergens , Antigens, Plant/analysis , Carrier Proteins/analysis , Cross Reactions , Humans , Plant Proteins/analysis
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