PD-1 on dendritic cells impedes innate immunity against bacterial infection

Author:

Yao Sheng1,Wang Shengdian2,Zhu Yuwen1,Luo Liqun1,Zhu Gefeng1,Flies Sarah1,Xu Haiying1,Ruff William1,Broadwater Megan1,Choi In-Hak3,Tamada Koji1,Chen Lieping1

Affiliation:

1. Department of Oncology and Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, MD;

2. Center for Infection and Immunity, Institute of Biophysics, Chinese Academy of Science, Beijing, China; and

3. Department of Microbiology, Inje University College of Medicine, Busan, Republic of Korea

Abstract

AbstractProgrammed death one (PD-1) is an inducible molecule belonging to the immunoglobulin superfamily. It is expressed on activated T and B lymphocytes and plays pivotal roles in the negative regulation of adaptive immune responses. We report here an unexpected finding: that PD-1 could also be induced on splenic dendritic cells (DCs) by various inflammatory stimuli. Adoptive transfer of PD-1–deficient DCs demonstrates their superior capacity to wild-type DCs in innate protection of mice against lethal infection by Listeria monocytogenes. Furthermore, PD-1–deficient mice are also more resistant to the infection than wild-type controls, even in the absence of T and B cells, accompanied by elevated production of DC-derived interleukin-12 and tumor necrosis factor-α. Our results reveal a novel role of PD-1 in the negative regulation of DC function during innate immune response.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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