Adaptation of Innate Lymphoid Cells to a Micronutrient Deficiency Promotes Type 2 Barrier Immunity

Sean P. Spencer(National Institute of Allergy and Infectious Diseases), Christoph Wilhelm(National Institute of Allergy and Infectious Diseases), Qi Yang(University of Pennsylvania), J. A. Hall(National Institute of Allergy and Infectious Diseases), Nicolas Bouladoux(National Institute of Allergy and Infectious Diseases), Alexis Boyd(National Institute of Allergy and Infectious Diseases), Nutman Tb(National Institute of Allergy and Infectious Diseases), Joseph F. Urban(Beltsville Human Nutrition Research Center), Jie-lin Wang(University of California, Berkeley), T. R. Ramalingam(National Institute of Allergy and Infectious Diseases), Avinash Bhandoola(University of Pennsylvania), Thomas A. Wynn(National Institute of Allergy and Infectious Diseases), Yasmine Belkaid(National Institute of Allergy and Infectious Diseases)
Science
January 23, 2014
Cited by 436

Abstract

How the immune system adapts to malnutrition to sustain immunity at barrier surfaces, such as the intestine, remains unclear. Vitamin A deficiency is one of the most common micronutrient deficiencies and is associated with profound defects in adaptive immunity. Here, we found that type 3 innate lymphoid cells (ILC3s) are severely diminished in vitamin A-deficient settings, which results in compromised immunity to acute bacterial infection. However, vitamin A deprivation paradoxically resulted in dramatic expansion of interleukin-13 (IL-13)-producing ILC2s and resistance to nematode infection in mice, which revealed that ILCs are primary sensors of dietary stress. Further, these data indicate that, during malnutrition, a switch to innate type 2 immunity may represent a powerful adaptation of the immune system to promote host survival in the face of ongoing barrier challenges.


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