Methods: Female Balb/c mice were maintained fasting for 7 hours and then sensitized with active Bromelain through intragastric route, once a week per 8 consecutive weeks. The body weight and blood sample are collected in 0, 21, 42 and 56 days. In day 56, animals were challenge by oral route with active Bromelain or fresh A.comosus (pineapple) extract . Early signals, rectal temperature and respiratory parameters (by Whole-body plethysmograph) were measured by up to 45 minutes.IgG1 and IgG2a specific-antibodies were quantified by ELISA and anaphylatic antibodies title was obtain by Active Anaphylaxis Cutaneous (ACA). Histological methods were realized for measure infiltrate in stomach and small intestine.
Results: Bromelain group mice were underweight when compared to the saline group. The oral challenge (day 56) promoted a drop of the body temperature when mice were challenge to both Bromelain and fresh pineapple extract. Decreases in expiratory time and relation time were induced by oral challenge with protease. Specific IgG1 and IgG2a were detected in the serum of sensitized mice. Antibodies produced in response to Bromelain promoted a positive and high title of anaphylactic antibodies (1/40) by ACA for fresh A.comosus extract and a smaller title for Bromelain. In addition, after 24 hour to oral challenge, sensitized mice presented infiltrate inflammatory cells in stomach and small intestine.
Conclusions: Using the mouse model of food allergy previously developed by us, we describe here the ability of majority protease Ananas, Bromelain, in breakdown oral tolerance and functions as Th2 adjuvant, sensitizing mice to respond positively after challenge to both fresh A. comosus extract and Bromelain.
Financial support: FAPESP and Institute for Investigation in Immunology (iii)–INCT-CNPq