Intestinal microenvironment-mediated allergic dynamic phenotypes and endotypes in the development of gluten allergy

This study aimed to investigate the dynamic changes in intestinal microenvironment factors in the development of gluten-induced allergy (GA). Our results showed that GA provoked increasingly severe allergic phenotypes such as allergic and diarrheal symptoms with the gluten sensitization frequency, which was accompanied by dynamically rising levels of gluten-specific immunoglobulin (Ig) E, IgG2a and IgA, serum histamine, T cellrelated inflammatory cytokines, and intestinal indexes. An increase in luminal pH was more significant in the large intestine versus the small intestine, which was due to a dynamic decline in colonic short-chain fatty acid levels. Both antioxidant capacity and intestinal permeability in the large intestine varied with the GA severity, as evidenced by a dynamic increase in the malondialdehyde content and a decrease in the superoxide dismutase activity and total antioxidant capacity. Moreover, we demonstrated that intestinal microenvironment dysbiosis occurred before a true allergy reaction began. Spearman correlation analysis suggested that the characteristic bacterial cluster, namely Alistipes, Desulfovibrio, Ileibacterium, Parabacteroides, and Ruminococcus torques group, are essential in the association between GA and intestinal microenvironment homeostasis.

Automated summary

The study investigated the dynamic changes in intestinal microenvironment factors during the development of gluten-induced allergy (GA). Results showed that the severity of allergic symptoms and diarrhea increased with gluten sensitization frequency, along with rising levels of gluten-specific immunoglobulins, histamine, inflammatory cytokines, and intestinal markers. Dysbiosis of the intestinal microbiome occurred before the onset of true allergic reactions, and specific bacterial clusters were found to be essential in the association between GA and intestinal homeostasis.