T cell immunotherapy for melanoma from bedside to bench to barn and back: how conceptual advances in experimental mouse models can be translated into clinical benefit for patients

Pigment Cell Melanoma Res. 2013 Jul;26(4):441-56. doi: 10.1111/pcmr.12111. Epub 2013 May 15.

Abstract

A solid scientific basis now supports the concept that cytotoxic T lymphocytes can specifically recognize and destroy melanoma cells. Over the last decades, clinicians and basic scientists have joined forces to advance our concepts of melanoma immunobiology. This has catalyzed the rational development of therapeutic approaches to enforce melanoma-specific T cell responses. Preclinical studies in experimental mouse models paved the way for their successful translation into clinical benefit for patients with metastatic melanoma. A more thorough understanding of how melanomas develop resistance to T cell immunotherapy is necessary to extend this success. This requires a continued interdisciplinary effort of melanoma biologists and immunologists that closely connects clinical observations with in vitro investigations and appropriate in vivo mouse models: From bedside to bench to barn and back.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antigens, Neoplasm / chemistry
  • Cancer Vaccines
  • Carcinogens / chemistry
  • Dendritic Cells / cytology
  • Granulocyte-Macrophage Colony-Stimulating Factor / metabolism
  • Humans
  • Immunotherapy / methods*
  • Melanoma / immunology*
  • Melanoma / therapy*
  • Melanoma, Experimental
  • Mice
  • Mutation
  • Sarcoma / immunology
  • Sarcoma / therapy
  • T-Lymphocytes, Cytotoxic / cytology*
  • Translational Research, Biomedical / trends

Substances

  • Antigens, Neoplasm
  • Cancer Vaccines
  • Carcinogens
  • Granulocyte-Macrophage Colony-Stimulating Factor