Programmed death 1 and B and T lymphocyte attenuator immunoreceptors and their association with malignant T-lymphoproliferative disorders: brief review

Hematol Oncol. 2014 Sep;32(3):113-9. doi: 10.1002/hon.2098. Epub 2013 Sep 13.

Abstract

Malignant T-cell lymphoproliferative diseases are relatively rare. T cells are activated through the T-cell receptor with the aid of costimulating molecules that can be either excitatory or inhibitory. Such pathways have been also implicated in mechanisms of malignant T-cell lymphoproliferative diseases' persistence and relapse by circumventing immune responses. To date, three major immunoinhibitory molecules have been recognized, namely programmed cell death-1 (PD-1), B and T lymphocyte attenuator (BTLA) and cytotoxic T lymphocyte antigen 4 (CTLA-4). Although CTLA-4 is considered the 'gatekeeper' of immune tolerance, PD-1 negatively regulates immune responses broadly, whereas BTLA activation has been shown to inhibit CD8+ cancer-specific T cells. Both PD-1 and BTLA downregulate proximal T-cell receptor signalling cascade and are involved in immune evasion of leukaemias and lymphomas, even after allogeneic stem cell transplantation. These immunoregulatory molecules can have seemingly a synergistic effect on weakening the immune response of patients with haematological malignancies, and their manipulation represents a very active field of preclinical as well as clinical interest.

Keywords: immune evasion; immunoinhibitory molecules; malignant T-cell lymphoproliferative diseases.

Publication types

  • Review

MeSH terms

  • Animals
  • Communicable Diseases / genetics
  • Communicable Diseases / immunology
  • Communicable Diseases / metabolism
  • Humans
  • Immune System Diseases / genetics
  • Immune System Diseases / immunology
  • Immune System Diseases / metabolism
  • Lymphoproliferative Disorders / genetics
  • Lymphoproliferative Disorders / immunology
  • Lymphoproliferative Disorders / metabolism*
  • Monitoring, Immunologic
  • Neoplasms / genetics
  • Neoplasms / immunology
  • Neoplasms / metabolism
  • Programmed Cell Death 1 Receptor / genetics
  • Programmed Cell Death 1 Receptor / metabolism*
  • Receptors, Immunologic / genetics
  • Receptors, Immunologic / metabolism*
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism*
  • T-Lymphocytes / pathology*
  • Tumor Escape

Substances

  • BTLA protein, human
  • Programmed Cell Death 1 Receptor
  • Receptors, Immunologic