International Journal of Molecular Sciences (Jan 2021)

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

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

DOI
https://doi.org/10.3390/ijms22031426
Journal volume & issue
Vol. 22, no. 3
p. 1426

Abstract

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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.

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