Deficiency in T follicular regulatory cells promotes autoimmunity

Author:

Fu Weiwei1,Liu Xindong2,Lin Xiang3ORCID,Feng Han1ORCID,Sun Lin1,Li Shuran4,Chen Hairong4,Tang Hong5,Lu Liwei3ORCID,Jin Wei1,Dong Chen1ORCID

Affiliation:

1. Institute for Immunology and School of Medicine, Tsinghua University, Beijing, China

2. Institute of Pathology and Southwest Cancer Center, Southwest Hospital, Third Military Medical University, Chongqing, China

3. Department of Pathology and Shenzhen Institute of Research and Innovation, University of Hong Kong, Hong Kong, China

4. CAS Key Laboratory of Infection and Immunity, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China

5. CAS Key Laboratory of Molecular Virology and Immunology, Institute Pasteur of Shanghai, Chinese Academy of Sciences, Beijing, China

Abstract

T follicular regulatory (Tfr) cells are a new subset of regulatory T (T reg) cells localized in the germinal center to limit the humoral response. Until now, the physiological function of Tfr cells has been largely unknown. In this study, we developed a Bcl6fl/flFoxp3Cre mouse to analyze the function of Tfr cells in immune and autoimmune responses. These mice exhibited enhanced immunity to influenza virus; moreover, Bcl6fl/flFoxp3Cre/Cre mice developed late-onset spontaneous autoimmune diseases, affecting the salivary glands with lymphocyte infiltration and antibody deposition. In a mouse experimental Sjögren’s syndrome model, ablation of Bcl6 in T reg cells greatly enhanced disease development. Conversely, Bcl6fl/flCd4Cre mice were protected in the model. Thus, our study indicates that Tfr cells control autoimmune diseases and can be targeted in infectious and autoimmune disease.

Funder

National Natural Science Foundation of China

Chinese Ministry of Science and Technology

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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