Correspondingly, the Register has very few reports of adverse reactions caused by green pea or soy, a substantial number of reports regarding lupin selleck inhibitor and fenugreek, and many regarding peanut. These data show that there is a need to further investigate cross-allergy in legumes. Most of the work performed on legume allergy has focused on peanut as the major allergenic legume, and information on other

types of legume allergy is limited [4]. As we previously have established mouse models of lupin and fenugreek allergy [25, 26], we used these models to address the clinical cross-allergy between the four most common allergenic legumes: lupin, fenugreek, peanut and soy. We also assessed different serological and cellular responses to explore possible mechanisms related to the cross-allergic reactions. Animals.  Female inbred C3H/HeJ mice (Jackson Laboratories, Bar Harbor, ME, USA), 5 weeks old at the start of the experiments, were used. Several experiments have been combined in this study and an account of the animals with immunizations and challenges is therefore given in Table 1. Female Sprague-Dawley rats, 150–200 g (Taconic M&B A/S, Ry, Denmark) were used to perform the passive cutaneous anaphylaxis (PCA) tests. The animals were housed, 3–4

mice or two rats per cage, on NESTPAK bedding (Datesand Ltd, Manchester, UK) in type III macrolon cages in filter cabinets (Scantainers), exposed to a 12-hr/12-hr light/dark cycle very (30–60 lux in cages), room temperature of 21 ± 2 °C and 35–75% humidity. Pelleted food (RM1; PLX3397 SDS, Essex, UK) and tap water ad libitum were given. Before entering the experiments, the animals were allowed to rest for 1 week. The experiments were performed in conformity with the laws and regulations for experiments with live animals in Norway and were approved by the Norwegian Animal Research Authority under the Ministry of Agriculture. Legume extracts.  The National Veterinary Institute of Norway provided all protein extracts. In short, extracts of peanut, lupin and soy were made by extracting

homogenized peanuts, soybeans or lupin (Lupinus angustifolius) in Tris/glycine buffer, pH 8.7, overnight followed by centrifugation. The fenugreek extract was made using an extended protocol utilizing precipitation with (NH4)2SO4, dialysis and freeze-drying [26]. The total protein concentration of the extracts was measured by Lowry’s method. The endotoxin level of the extract was determined with the Limulus Amebocyte Lysate (LAL) Kinetic-QCL Kit (BioWhittaker, Walkersville, MD, USA) and found to be below 0.1 ng/ml for all extracts. Immunizations and challenges.  Immunizations were performed perorally (p.o.) according to the experimental protocols previously established [25, 26]. Briefly, immunizations were performed on days 0, 1, 2, 7, 21 and 28 and challenges on day 35. Lupin immunized mice received 5.