Absence of MHC class II on cDCs results in microbial-dependent intestinal inflammation

Author:

Loschko Jakob1,Schreiber Heidi A.1,Rieke Gereon J.12,Esterházy Daria3,Meredith Matthew M.1,Pedicord Virginia A.3,Yao Kai-Hui1,Caballero Silvia4,Pamer Eric G.4,Mucida Daniel3,Nussenzweig Michel C.15

Affiliation:

1. Laboratory of Molecular Immunology, The Rockefeller University, New York, NY, 10065

2. Rheinische Friedrich-Wilhelms University Bonn, 53113 Bonn, Germany

3. Laboratory of Mucosal Immunology, The Rockefeller University, New York, NY, 10065

4. Immunology Program, Sloan Kettering Institute Infectious Diseases Service Clinical Microbiology Laboratory, Memorial Sloan Kettering Cancer Center, New York, NY, 10065

5. Howard Hughes Medical Institute, The Rockefeller University, New York, NY, 10065

Abstract

Conventional dendritic cells (cDCs) play an essential role in host immunity by initiating adaptive T cell responses and by serving as innate immune sensors. Although both innate and adaptive functions of cDCs are well documented, their relative importance in maintaining immune homeostasis is poorly understood. To examine the significance of cDC-initiated adaptive immunity in maintaining homeostasis, independent of their innate activities, we generated a cDC-specific Cre mouse and crossed it to a floxed MHC class II (MHCII) mouse. Absence of MHCII on cDCs resulted in chronic intestinal inflammation that was alleviated by antibiotic treatment and entirely averted under germ-free conditions. Uncoupling innate and adaptive functions of cDCs revealed that innate immune functions of cDCs are insufficient to maintain homeostasis and antigen presentation by cDCs is essential for a mutualistic relationship between the host and intestinal bacteria.

Funder

National Institutes of Health

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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