The T-win® technology: immune-modulating vaccines

21 Citations (Scopus)

Abstract

The T-win® technology is an innovative investigational approach designed to activate the body's endogenous anti-regulatory T cells (anti-Tregs) to target regulatory as well as malignant cells. Anti-Tregs are naturally occurring T cells that can directly react against regulatory immune cells because they recognize proteins that these targets express, including indoleamine 2,3-dioxygenase (IDO), tryptophan 2,6-dioxygenase, arginase, and programmed death ligand 1 (PD-L1). The T-win® technology is characterized by therapeutic vaccination with long peptide epitopes derived from these antigens and therefore offers a novel way to target genetically stable cells with regular human leukocyte antigen expression in the tumor microenvironment. The T-win® technology thus also represents a novel way to attract pro-inflammatory cells to the tumor microenvironment where they can directly affect immune inhibitory pathways, potentially altering tolerance to tumor antigens. The modification of an immune regulatory environment into a pro-inflammatory milieu potentiates effective anti-tumor T cell responses. Many regulatory immune cells may be reverted into effector cells given the right stimulus. Because T-win® technology is based on the immune-modulatory function of the vaccines, the vaccines activate both CD4 and CD8 anti-Tregs. Of importance, in clinical trials, vaccinations against IDO or PD-L1 to potentiate anti-Tregs have so far proved to be safe, with minimal toxicity.

Original languageEnglish
JournalSeminars in Immunopathology
Volume41
Issue number1
Pages (from-to)87-95
Number of pages8
ISSN1863-2297
DOIs
Publication statusPublished - Jan 2019

Keywords

  • Anti-Tregs
  • Arginase
  • IDO
  • Immune-modulating vaccines
  • PD-L1
  • T-win technology
  • Immunotherapy/methods
  • Humans
  • Cancer Vaccines/administration & dosage
  • T-Lymphocytes, Regulatory/immunology
  • Biomarkers, Tumor
  • Animals
  • Energy Metabolism
  • Immunomodulation/drug effects
  • T-Lymphocyte Subsets/immunology
  • Neoplasms/immunology

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