“…Many studies on the gut have reported changes to the immune phenotype, with deficits of both the innate and adaptive immune components of the intestinal mucosa in GF mice. Several bacterial species have been shown to have different modulatory effects on the host immune system, highlighting the need for specific bacteria within a given developmental window for the normal patterning of host immunity ( Olszak et al, 2012 ; Ubags and Marsland, 2017 ). GF mice have a thinner lamina propria, with fewer resident mature immune cells, and the presence of a complex microbiota triggers the proliferation, differentiation, and maturation of immune cells, leading to an increase in microbiota-selected IgA + (immunoglobulin A) plasma cells or T-cell subsets, such as T reg Foxp3, Th1 (T-helper), Th2, and Th17 lymphocytes ( Macpherson and Uhr, 2004 ; Gaboriau-Routhiau et al, 2009 ; Ivanov et al, 2009 ).…”