Immunotherapy Resistance by Inflammation-Induced Dedifferentiation

Cancer Discov. 2018 Aug;8(8):935-943. doi: 10.1158/2159-8290.CD-17-1178. Epub 2018 Jun 13.

Abstract

A promising arsenal of targeted and immunotherapy treatments for metastatic melanoma has emerged over the last decade. With these therapies, we now face new mechanisms of tumor-acquired resistance. We report here a patient whose metastatic melanoma underwent dedifferentiation as a resistance mechanism to adoptive T-cell transfer therapy (ACT) to the MART1 antigen, a phenomenon that had been observed only in mouse studies to date. After an initial period of tumor regression, the patient presented in relapse with tumors lacking melanocytic antigens (MART1, gp100) and expressing an inflammation-induced neural crest marker (NGFR). We demonstrate using human melanoma cell lines that this resistance phenotype can be induced in vitro by treatment with MART1 T cell receptor-expressing T cells or with TNFα, and that the phenotype is reversible with withdrawal of inflammatory stimuli. This supports the hypothesis that acquired resistance to cancer immunotherapy can be mediated by inflammation-induced cancer dedifferentiation.Significance: We report a patient whose metastatic melanoma underwent inflammation-induced dedifferentiation as a resistance mechanism to ACT to the MART1 antigen. Our results suggest that future melanoma ACT protocols may benefit from the simultaneous targeting of multiple tumor antigens, modulating the inflammatory response, and inhibition of inflammatory dedifferentiation-inducing signals. Cancer Discov; 8(8); 935-43. ©2018 AACR.This article is highlighted in the In This Issue feature, p. 899.

Trial registration: ClinicalTrials.gov NCT00910650.

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Dedifferentiation
  • Cell Line, Tumor
  • Coculture Techniques
  • Drug Resistance, Neoplasm*
  • Humans
  • Immunotherapy, Adoptive
  • MART-1 Antigen / immunology*
  • Male
  • Melanoma / immunology
  • Melanoma / therapy*
  • Middle Aged
  • Neoplasm Metastasis
  • Nerve Tissue Proteins / metabolism*
  • Nevus, Pigmented / immunology
  • Nevus, Pigmented / therapy*
  • Receptors, Chimeric Antigen / metabolism
  • Receptors, Nerve Growth Factor / metabolism*
  • Recurrence

Substances

  • MART-1 Antigen
  • MLANA protein, human
  • NGFR protein, human
  • Nerve Tissue Proteins
  • Receptors, Chimeric Antigen
  • Receptors, Nerve Growth Factor

Associated data

  • ClinicalTrials.gov/NCT00910650