Programmed Death-Ligand 2 Deficiency Exacerbates Experimental Autoimmune Myocarditis in Mice

Author:

Li Siqi,Tajiri KazukoORCID,Murakoshi Nobuyuki,Xu DongZhu,Yonebayashi Saori,Okabe Yuta,Yuan Zixun,Feng Duo,Inoue Keiko,Aonuma Kazuhiro,Shimoda Yuzuno,Song Zoughu,Mori Haruka,Huang Honglan,Aonuma KazutakaORCID,Ieda MasakiORCID

Abstract

Programmed death ligand 2 (PD-L2) is the second ligand of programmed death 1 (PD-1) protein. In autoimmune myocarditis, the protective roles of PD-1 and its first ligand programmed death ligand 1 (PD-L1) have been well documented; however, the role of PD-L2 remains unknown. In this study, we report that PD-L2 deficiency exacerbates myocardial inflammation in mice with experimental autoimmune myocarditis (EAM). EAM was established in wild-type (WT) and PD-L2-deficient mice by immunization with murine cardiac myosin peptide. We found that PD-L2-deficient mice had more serious inflammatory infiltration in the heart and a significantly higher myocarditis severity score than WT mice. PD-L2-deficient dendritic cells (DCs) enhanced CD4+ T cell proliferation in the presence of T cell receptor and CD28 signaling. These data suggest that PD-L2 on DCs protects against autoreactive CD4+ T cell expansion and severe inflammation in mice with EAM.

Funder

Japan Society for the Promotion of Science

KANAE Foundation for the Promotion of Medical Science

Bayer Scholarship for Cardiovascular Research

Takeda Science Foundation

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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