Opening up new VISTAs: V-domain immunoglobulin suppressor of T cell activation (VISTA) targeted near-infrared photoimmunotherapy (NIR-PIT) for enhancing host immunity against cancers

Cancer Immunol Immunother. 2022 Dec;71(12):2869-2879. doi: 10.1007/s00262-022-03205-5. Epub 2022 Apr 21.

Abstract

V-domain immunoglobulin suppressor of T cell activation (VISTA) is an inhibitory immune checkpoint molecule that is broadly expressed on lymphoid and myeloid cells, including regulatory T cells (Tregs) and myeloid-derived suppressor cells (MDSCs). Near-infrared photoimmunotherapy (NIR-PIT) is a cancer treatment that utilizes an antibody-photoabsorber (IRDye 700DX NHS ester) conjugate to selectively kill target cells after the local application of NIR light. Depletion of VISTA-expressing cells in the tumor microenvironment (TME) using NIR-PIT could enhance anti-tumor immune responses by removing immune suppressive cells. The purpose of this study was to evaluate the anti-tumor efficacy of VISTA-targeted NIR-PIT using two murine tumor models, MC38-luc and LL2-luc. VISTA was expressed on T cells including Tregs and MDSCs in the TME of these tumors. In contrast, CD45 - cells, including cancer cells, did not express VISTA. VISTA-targeted NIR-PIT depleted VISTA-expressing cells ex vivo. In vivo VISTA-targeted NIR-PIT inhibited tumor progression and prolonged survival in both models. After VISTA-targeted NIR-PIT, augmented CD8 + T cell and dendritic cell activation were observed in regional lymph nodes. In conclusion, VISTA-targeted NIR-PIT can effectively treat tumors by decreasing VISTA-expressing immune suppressor cells in the TME. Local depletion of VISTA-expressing cells in the tumor bed using NIR-PIT is a promising new cancer immunotherapy for treating various types of tumors.

Keywords: Myeloid-derived suppressor cell (MDSC); Near-infrared photoimmunotherapy (NIR-PIT); Regulatory T cell (Treg); V-domain immunoglobulin suppressor of T cell activation (VISTA).

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Esters
  • Humans
  • Immune Checkpoint Proteins
  • Immunotherapy
  • Mice
  • Neoplasms* / therapy
  • T-Lymphocytes, Regulatory*
  • Xenograft Model Antitumor Assays

Substances

  • Immune Checkpoint Proteins
  • Esters