Differential Modulation of 25-hydroxycholecalciferol on Innate Immunity of Broiler Breeder Hens

Simple Summary No predominant changes between R- vs. Ad-feed intake on leukocyte defense against pathogens were observed in broiler breeder hens despite some differences in inflammatory and respiratory burst responses. Overall, supplemental 25-OH-D-3 had more pronounced effects on the innate immunity of Ad-hens. In vitro studies confirmed the differential effects of 25-OH-D-3 to rescue immune functions altered by glucose and/or palmitic acid exposure. Past immunological studies in broilers focused on juveniles within the rapid pre-slaughter growth period and may not reflect adult immune responses, particularly in breeders managed with chronic feed restriction (R). The study aimed to assess innate immune cell functions in respect to R vs. ad libitum (Ad) feed intake in breeder hens with and without dietary 25-hydroxycholecalciferol (25-OH-D-3) supplementation. Ad-feed intake consistently suppressed IL-1 beta secretion, respiratory burst, and cell livability in peripheral heterophils and/or monocytes along the feeding trial from the age of 51 to 68 weeks. Supplemental 25-OH-D-3 repressed IL-1 beta secretion and respiratory burst of both cells mostly in R-hens, but promoted monocyte phagocytosis, chemotaxis, and bacterial killing activity in Ad-hens in accompany with relieved hyperglycemia, hyperlipidemia, and systemic inflammation. Overnight cultures with leukocytes from R-hens confirmed the differential effects of 25-OH-D-3 to rescue immune functions altered by glucose and/or palmitic acid exposure. Studies with specific inhibitors further manifested the operative mechanisms via glucolipotoxicity in a cell type- and function-dependent manner. The results concluded no predominant changes between R- vs. Ad-feed intake on leukocyte defense against pathogens despite some differential differences, but supplemental 25-OH-D-3 exerts more pronounced effects in Ad-hens.

Automated summary

The study found that ad-libitum feed intake suppressed IL-1 beta secretion, respiratory burst, and cell livability in white blood cells, while supplemental 25-OH-D-3 had more pronounced effects on innate immunity. In vitro studies confirmed the differential effects of 25-OH-D-3 on rescuing immune functions altered by glucose and/or palmitic acid exposure.