1. Academic Validation
  2. RGMb is a novel binding partner for PD-L2 and its engagement with PD-L2 promotes respiratory tolerance

RGMb is a novel binding partner for PD-L2 and its engagement with PD-L2 promotes respiratory tolerance

  • J Exp Med. 2014 May 5;211(5):943-59. doi: 10.1084/jem.20130790.
Yanping Xiao 1 Sanhong Yu Baogong Zhu Denis Bedoret Xia Bu Loise M Francisco Ping Hua Jonathan S Duke-Cohan Dale T Umetsu Arlene H Sharpe Rosemarie H DeKruyff Gordon J Freeman
Affiliations

Affiliation

  • 1 Department of Medical Oncology, Dana-Farber Cancer Institute; 2 Division of Immunology and Department of Pediatrics, Boston Children's Hospital; 3 Department of Microbiology and Immunobiology and 4 Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115.
Abstract

We report that programmed death ligand 2 (PD-L2), a known ligand of PD-1, also binds to repulsive guidance molecule b (RGMb), which was originally identified in the nervous system as a co-receptor for bone morphogenetic proteins (BMPs). PD-L2 and BMP-2/4 bind to distinct sites on RGMb. Normal resting lung interstitial macrophages and alveolar epithelial cells express high levels of RGMb mRNA, whereas lung dendritic cells express PD-L2. Blockade of the RGMb-PD-L2 interaction markedly impaired the development of respiratory tolerance by interfering with the initial T cell expansion required for respiratory tolerance. Experiments with PD-L2-deficient mice showed that PD-L2 expression on non-T cells was critical for respiratory tolerance, but expression on T cells was not required. Because PD-L2 binds to both PD-1, which inhibits antitumor immunity, and to RGMb, which regulates respiratory immunity, targeting the PD-L2 pathway has therapeutic potential for asthma, Cancer, and Other immune-mediated disorders. Understanding this pathway may provide insights into how to optimally modulate the PD-1 pathway in Cancer Immunotherapy while minimizing adverse events.

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